Solids & Liquids

Preparation for General Chemistry · Dr. Karmach

Dr. Karmach

By the end of this unit, you can…

  • Name the six changes of state, label each endothermic or exothermic, and read a heating or cooling curve
  • Calculate the heat for warming steps with q = mcΔT and for phase changes with the heats of fusion and vaporization, and add them along a heating curve
  • Identify the intermolecular forces in a substance and rank substances by boiling point and vapor pressure
  • Explain vapor pressure, boiling point, surface tension, and viscosity from intermolecular forces, including why boiling point changes with outside pressure
  • Read a phase diagram: the stable phase at a given pressure and temperature, the triple point, and the normal melting and boiling points
  • Classify a solid as ionic, metallic, molecular, or network and predict its melting point, hardness, and conductivity
Dr. Karmach

Today's route 🗺️

  1. Intermolecular Forces
  2. Properties of Liquids
  3. IMFs & Boiling Point
  4. Phase Diagrams
  5. Heat of a Phase Change
  6. Heating & Cooling Curves
  7. Types of Solids
Dr. Karmach

1 · Intermolecular Forces

Identify which intermolecular forces a substance has and name the strongest one present, keeping these attractions between molecules distinct from the bonds inside them.

Dr. Karmach

Why water beads and geckos climb

Water beads up on a waxed car. A gecko walks up a glass wall. Faint attractions between molecules, far weaker than the bonds inside them, hold and lift.

Dr. Karmach

What decides solid, liquid, or gas

Particles are always moving, and they attract one another. When motion wins, the particles fly apart as a gas. When attraction wins, they stay in contact as a liquid or a solid.

at room temperature: CH₄ (16.04 g/mol) is a gas · H₂O (18.02 g/mol) is a liquid
nearly the same mass · water molecules attract one another far more strongly
Dr. Karmach

Forces between molecules, not the bonds within

An intermolecular force is an attraction between separate molecules. It is always weaker than the covalent bond holding one molecule together. Melting and boiling loosen these forces; the bonds inside stay intact.

Dr. Karmach

The four kinds, weakest to strongest

Every substance has London dispersion. Polar molecules add dipole–dipole. An H on N, O, or F adds hydrogen bonding. Dissolved ions give ion–dipole, the strongest.

memory hook: I Hate Doing Laundry, strongest first
Ion–dipole > Hydrogen bonding > Dipole–dipole > London dispersion
Dr. Karmach

Dispersion grows with size

London dispersion comes from the electron cloud shifting for an instant. A bigger, heavier cloud shifts more easily, so dispersion strengthens as molar mass rises. Among the nonpolar halogens, it climbs straight down the group.

F₂ · Cl₂ · Br₂ · I₂: all nonpolar
molar mass 38.00 → 70.90 → 159.80 → 253.80 g/mol · dispersion rises with it
Dr. Karmach

The method

  1. Identify the pieces. Ions in a polar solvent, or molecules? Polar? Any H on N, O, or F?
  2. Name every force present. Dispersion always; dipole–dipole if polar; hydrogen bonding if H–N/O/F; ion–dipole for dissolved ions.
  3. Pick the strongest.

Dr. Karmach

Guided example: chloroform

CHCl₃: carbon bonded to one H and three Cl
tetrahedral · wanted: every force present, and the strongest

Chloroform was one of the first surgical anesthetics. Name every intermolecular force in liquid chloroform, then the strongest.

Scan in order: an ion first, then an H on N, O, or F, then polarity.

Dr. Karmach

Guided example: identify the pieces

CHCl₃: carbon bonded to one H and three Cl
tetrahedral · wanted: every force present, and the strongest

Step 1 · Identify the pieces

an ion in a polar solvent? no
move 1 · CHCl₃ is a neutral molecule, not a dissolved ion
Dr. Karmach

Guided example: identify the pieces

CHCl₃: carbon bonded to one H and three Cl
tetrahedral · wanted: every force present, and the strongest

Step 1 · Identify the pieces

an ion in a polar solvent? no
move 1 · CHCl₃ is a neutral molecule, not a dissolved ion
H bonded to N, O, or F? no
move 2 · the only H sits on carbon · Cl is not N, O, or F
Dr. Karmach

Guided example: identify the pieces

CHCl₃: carbon bonded to one H and three Cl
tetrahedral · wanted: every force present, and the strongest

Step 1 · Identify the pieces

an ion in a polar solvent? no
move 1 · CHCl₃ is a neutral molecule, not a dissolved ion
H bonded to N, O, or F? no
move 2 · the only H sits on carbon · Cl is not N, O, or F
polar molecule? yes
move 3 · one H and three Cl around carbon · the bond dipoles do not cancel
Dr. Karmach

Guided example: identify the pieces

CHCl₃: carbon bonded to one H and three Cl
tetrahedral · wanted: every force present, and the strongest

Step 1 · Identify the pieces

an ion in a polar solvent? no
move 1 · CHCl₃ is a neutral molecule, not a dissolved ion
H bonded to N, O, or F? no
move 2 · the only H sits on carbon · Cl is not N, O, or F
polar molecule? yes
move 3 · one H and three Cl around carbon · the bond dipoles do not cancel
Three questions, answered no, no, yes. The first yes is polarity.
Dr. Karmach

Guided example: name the forces

CHCl₃: a neutral, polar molecule
no ion · no H on N, O, or F · polar

Step 2 · Name every force present

polar · H on C only → London dispersion + dipole–dipole

Dispersion is in every substance. Polarity adds dipole–dipole.

Dr. Karmach

Guided example: name the forces

CHCl₃: a neutral, polar molecule
no ion · no H on N, O, or F · polar
Step 2 · Name every force present
polar · H on C only → London dispersion + dipole–dipole
Step 3 · Pick the strongest
CHCl₃ → strongest force: dipole–dipole
dipole–dipole outranks dispersion · no hydrogen bonding, no ion–dipole
Dr. Karmach

Guided example: name the forces

CHCl₃: a neutral, polar molecule
no ion · no H on N, O, or F · polar
Step 2 · Name every force present
polar · H on C only → London dispersion + dipole–dipole
Step 3 · Pick the strongest
CHCl₃ → strongest force: dipole–dipole
dipole–dipole outranks dispersion · no hydrogen bonding, no ion–dipole
Chloroform holds three Cl atoms, but Cl is not a hydrogen-bond atom and the H sits on carbon. Dipole–dipole is the strongest. ✓
Dr. Karmach

Guided example: the route on the chart

CHCl₃: carbon bonded to one H and three Cl
found: dispersion + dipole–dipole · strongest: dipole–dipole

No, no, yes: chloroform exits at dipole–dipole. Dispersion comes along, as it does in every substance. ✓
Dr. Karmach

Worked example 1: methane

CH₄: carbon bonded to four hydrogens
tetrahedral · four identical C–H bonds · wanted: forces present, and the strongest

Natural gas is mostly methane. Name every intermolecular force it has, then the strongest.

Dr. Karmach

Worked example 1: solution

CH₄: carbon bonded to four hydrogens
tetrahedral · four identical C–H bonds

Step 1 · Identify the pieces

Methane is a molecule, not ions in a solvent. Its four C–H bonds sit in a symmetric tetrahedron, so the molecule is nonpolar. No H is bonded to N, O, or F.

Dr. Karmach

Worked example 1: solution

CH₄: carbon bonded to four hydrogens
tetrahedral · four identical C–H bonds
Step 1 · Identify the pieces Step 2 · Name every force present
nonpolar · no ionic pieces → London dispersion only

Dispersion is present in every substance. Nothing here adds dipole–dipole, hydrogen bonding, or ion–dipole.

Dr. Karmach

Worked example 1: solution

CH₄: carbon bonded to four hydrogens
tetrahedral · four identical C–H bonds
Step 1 · Identify the pieces Step 2 · Name every force present
nonpolar · no ionic pieces → London dispersion only
Step 3 · Pick the strongest
CH₄ → strongest force: London dispersion
the only force present, so it is also the strongest
Dr. Karmach

Worked example 1: solution

CH₄: carbon bonded to four hydrogens
tetrahedral · four identical C–H bonds
Step 1 · Identify the pieces Step 2 · Name every force present
nonpolar · no ionic pieces → London dispersion only
Step 3 · Pick the strongest
CH₄ → strongest force: London dispersion
the only force present, so it is also the strongest
A nonpolar molecule with no ions has just one option. Dispersion is the whole story for methane.
Dr. Karmach

Worked example 1: the route on the chart

CH₄: carbon bonded to four hydrogens
found: London dispersion only · strongest: London dispersion

Three "no" answers run straight across to dispersion only. A symmetric molecule with every H on carbon has nothing stronger. ✓
Dr. Karmach

Worked example 2: methanol

CH₃OH: an O–H group on a carbon
polar molecule · wanted: forces present, and the strongest

Methanol is the alcohol in some racing fuels. It is polar, so it has dipole–dipole attraction.

A common first answer: polar, so dipole–dipole is the strongest. Test it against the method.

Dr. Karmach

Worked example 2: forces present

CH₃OH: an O–H group on a carbon
polar molecule · the H sits directly on O

A common first answer

strongest force = dipole–dipole?
true for a polar molecule with no H on N, O, or F, but methanol has an O–H ✗

Methanol is polar, so dipole–dipole is real. It is not the strongest, because the H bonded to oxygen does more.

Dr. Karmach

Worked example 2: forces present

CH₃OH: an O–H group on a carbon
polar molecule · the H sits directly on O
A common first answer
strongest force = dipole–dipole?
true for a polar molecule with no H on N, O, or F, but methanol has an O–H ✗
Step 1 · Identify the pieces

A molecule, not ions. Polar. And one H is bonded directly to O: the trigger for hydrogen bonding.

Dr. Karmach

Worked example 2: forces present

CH₃OH: an O–H group on a carbon
polar molecule · the H sits directly on O
A common first answer
strongest force = dipole–dipole?
true for a polar molecule with no H on N, O, or F, but methanol has an O–H ✗
Step 1 · Identify the pieces Step 2 · Name every force present
dispersion · dipole–dipole · hydrogen bonding (H on O) → three forces present
Every molecule has dispersion. Polar adds dipole–dipole; the O–H adds hydrogen bonding on top.
Dr. Karmach

Worked example 2: the strongest force

CH₃OH: three forces present
dispersion · dipole–dipole · hydrogen bonding (H on O)

Step 3 · Pick the strongest

CH₃OH → strongest force: hydrogen bonding
H–O present · a strong special dipole–dipole, above ordinary dipole–dipole and dispersion
An H on N, O, or F lifts the strongest force from dipole–dipole up to hydrogen bonding.
Dr. Karmach

Worked example 2: the route on the chart

CH₃OH: an O–H group on a carbon
found: dispersion + dipole–dipole + hydrogen bonding · strongest: hydrogen bonding

The scan stops at the second question. An H on O exits at hydrogen bonding before polarity is ever asked. ✓
Dr. Karmach

Take-home: hydrogen bonding needs H on N, O, or F

hydrogen bonding: H₂O · NH₃ · CH₃OH · none: CH₄ · CH₃OCH₃ · PH₃
memory hook: hydrogen bonding is FON · the H must sit directly on F, O, or N · an H on C, P, S, or Cl does not qualify

The dashed link, a hydrogen bond, joins one water's δ+ hydrogen to a lone pair on the next molecule's δ− oxygen. It is far weaker than the covalent O–H.

Dr. Karmach

Practice 1

CH₃F · HBr · H₂O₂ · SiH₄
fluoromethane · hydrogen bromide · hydrogen peroxide · silane

Which substance forms hydrogen bonds in the pure liquid?

  1. CH₃F
  2. H₂O₂
  3. HBr
  4. SiH₄
Dr. Karmach

Practice 1 answer: B

H₂O₂: H–O–O–H → hydrogen bonding · answer B
each H bonded directly to O · CH₃F: H on C · HBr: H on Br · SiH₄: H on Si

A has fluorine, but every H sits on carbon; the F carries no H. C puts H on bromine, which is not N, O, or F. D has four H atoms, all on silicon.

The H must sit on N, O, or F itself. One of those atoms somewhere in the formula is not enough. ✓
Dr. Karmach

Practice 1: the route on the chart

H₂O₂ → strongest force: hydrogen bonding · answer B
a molecule, no ion · each H bonded directly to O

An H on O exits at the second question. The other three never reach that exit: their H atoms sit on C, Br, and Si. ✓
Dr. Karmach

Your turn: hydrogen sulfide

H₂S: bent, two S–H bonds
polar molecule · sulfur is not N, O, or F
step H₂S
1 · identify the pieces a molecule · polar · H bonded to
2 · name every force dispersion, plus
3 · pick the strongest

Fill the three cells. Watch the atom the H sits on.

Dr. Karmach

Your turn: hydrogen sulfide

H₂S: bent, two S–H bonds
polar molecule · sulfur is not N, O, or F
step H₂S
1 · identify the pieces a molecule · polar · H bonded to
2 · name every force dispersion, plus
3 · pick the strongest

Fill the three cells. Watch the atom the H sits on.

H₂S → strongest force: dipole–dipole
H on sulfur, not N/O/F → no hydrogen bonding · dispersion + dipole–dipole, strongest is dipole–dipole
Dr. Karmach

Where this goes wrong

Naming the covalent bond as the force between molecules. The bonds inside a molecule are intramolecular. They hold one molecule together and do not break when it melts or boils. Intermolecular forces act between molecules; melting and boiling loosen those.
Stopping at dipole–dipole when an H sits on N, O, or F. A polar molecule does have dipole–dipole. But an H bonded to nitrogen, oxygen, or fluorine upgrades the strongest force to hydrogen bonding, the stronger special case.
Defaulting to dispersion and missing the stronger force. Dispersion is in every molecule, but it is the weakest. Scan for an H on N, O, or F first, then for a dipole. The strongest present is the answer, not dispersion by default.
Ranking the forces in the wrong order. The order runs dispersion, dipole–dipole, hydrogen bonding, ion–dipole. Hydrogen bonding is not the strongest of all; ion–dipole outranks it.
Dr. Karmach

Practice 2

hydrogen fluoride, HF
a polar molecule · the single H is bonded to fluorine

What is the strongest intermolecular force present in HF?

  1. London dispersion: every molecule has it, so it must be the strongest
  2. Ordinary dipole–dipole: HF is polar, so dipole–dipole is as strong as it gets
  3. Hydrogen bonding: the H is bonded directly to fluorine, one of N, O, F
  4. The H–F covalent bond: that is the force holding the molecule to its neighbours
Dr. Karmach

Practice 2 answer: C

HF → strongest force: hydrogen bonding · answer C
H bonded directly to F · a strong special dipole–dipole, the strongest force here

B stopped one rung early: HF is polar, but the H bonded to fluorine upgrades the strongest force to hydrogen bonding, above ordinary dipole–dipole. A defaulted to the weakest force; dispersion is in every molecule but never the strongest when a stronger one is present. D named the H–F bond inside the molecule, which is intramolecular and does not act between molecules.

Scan from the top: an H on F means hydrogen bonding, and the scan stops there.
Dr. Karmach

Practice 2: the route on the chart

HF → strongest force: hydrogen bonding · answer C
a molecule, no ion · H bonded directly to F

An H on F exits at the second question. HF is polar too, but the scan never needs to ask. ✓
Dr. Karmach

Practice 3

PF₃: phosphorus bonded to three F
phosphorus trifluoride

Which list names every intermolecular force present in liquid PF₃?

  1. dispersion and dipole–dipole
  2. dispersion only
  3. dipole–dipole only
  4. dispersion, dipole–dipole, and hydrogen bonding
Dr. Karmach

Practice 3 answer: A

PF₃ → dispersion + dipole–dipole · answer A
a molecule, no ion · no H at all · one lone pair on P → trigonal pyramidal → polar

B treated PF₃ like BF₃: the lone pair on P makes it pyramidal, so the three P–F dipoles do not cancel. C left out dispersion, which every substance has. D counted the F as a hydrogen-bond trigger, but PF₃ has no H at all.

Two forces are present, and dipole–dipole is the stronger of them. ✓
Dr. Karmach

Practice 3: the route on the chart

PF₃ → dispersion + dipole–dipole · answer A
a molecule, no ion · no H at all · lone pair on P → polar

No, no, yes: PF₃ exits at dipole–dipole. Fluorine alone is not a yes at the second question; the H must be bonded to it. ✓
Dr. Karmach

Practice 4

CO₂ · CH₂F₂ · N₂H₄ · C₂H₆
carbon dioxide · difluoromethane · hydrazine · ethane

Which substance has dipole–dipole forces as its strongest intermolecular force?

  1. CO₂
  2. CH₂F₂
  3. N₂H₄
  4. C₂H₆
Dr. Karmach

Practice 4 answer: B

CH₂F₂ → strongest force: dipole–dipole · answer B
no ion · both H and both F bonded to C, so no H on F · two H and two F around carbon → polar

A has polar C=O bonds, but O=C=O is linear with matching ends: the dipoles cancel, leaving dispersion only. C is polar, but each H sits on N, so hydrogen bonding outranks dipole–dipole. D counted C–H as a polar bond; ethane is nonpolar, with dispersion only.

Only CH₂F₂ is polar with no H on N, O, or F. ✓
Dr. Karmach

Practice 4: the route on the chart

CH₂F₂ → strongest force: dipole–dipole · answer B
a molecule, no ion · H and F both bonded to C · lopsided → polar

CH₂F₂ holds fluorine, yet no H is bonded to F. Its first yes is polarity, so it exits at dipole–dipole. ✓
Dr. Karmach

Worked example 3: ranking three molecules

propane C₃H₈ · dimethyl ether CH₃OCH₃ · ethanol C₂H₅OH
molar mass ≈ 44, 46, 46 g/mol · wanted: rank by the strongest force each has

Three molecules of nearly equal molar mass. Rank them by the strength of the strongest intermolecular force in each, weakest first.

Dr. Karmach

Worked example 3: forces present

propane C₃H₈ · dimethyl ether CH₃OCH₃ · ethanol C₂H₅OH
molar mass ≈ 44, 46, 46 g/mol · dispersion is comparable in all three

Step 1 · Identify the pieces

Propane is a nonpolar hydrocarbon. Dimethyl ether is polar, but every H sits on carbon. Ethanol is polar and has an O–H.

Dr. Karmach

Worked example 3: forces present

propane C₃H₈ · dimethyl ether CH₃OCH₃ · ethanol C₂H₅OH
molar mass ≈ 44, 46, 46 g/mol · dispersion is comparable in all three
Step 1 · Identify the pieces Step 2 · Name every force present
propane → dispersion · ether → + dipole–dipole · ethanol → + hydrogen bonding
Each one has dispersion. The polar ether adds dipole–dipole; ethanol's O–H adds hydrogen bonding on top.
Dr. Karmach

Worked example 3: the ranking

propane · dimethyl ether · ethanol: same mass range
strongest force: dispersion < dipole–dipole < hydrogen bonding

Step 3 · Pick the strongest

Similar masses, so the strongest-force type sets the order: propane < dimethyl ether < ethanol.
Dr. Karmach

Worked example 3: the route on the chart

propane C₃H₈ · dimethyl ether CH₃OCH₃ · ethanol C₂H₅OH
found: dispersion < dipole–dipole < hydrogen bonding

Three molecules leave by three exits. Each exit names that molecule's strongest force, so the exits set the order: propane < dimethyl ether < ethanol. ✓
Dr. Karmach

Practice 5

argon (Ar) · formaldehyde (CH₂O) · methylamine (CH₃NH₂) · Na⁺ dissolved in water
CH₂O and CH₃NH₂ are polar molecules · rank weakest first

Which ranking orders the four by the strength of the strongest intermolecular force each one has, weakest first?

  1. Na⁺ in water < CH₃NH₂ < CH₂O < Ar
  2. Ar < CH₂O < Na⁺ in water < CH₃NH₂
  3. Na⁺ in water < CH₂O < CH₃NH₂ < Ar
  4. Ar < CH₂O < CH₃NH₂ < Na⁺ in water
Dr. Karmach

Practice 5 answer: D

Ar < CH₂O < CH₃NH₂ < Na⁺ in water · answer D
dispersion only · dipole–dipole · hydrogen bonding · ion–dipole

Argon is a lone nonpolar atom: dispersion only. CH₂O is polar, but both H atoms sit on carbon: dipole–dipole. CH₃NH₂ has H on N: hydrogen bonding. Na⁺ pulls on water's dipoles: ion–dipole.

B put hydrogen bonding at the top; ion–dipole outranks it. C ranked by molar mass, 22.99 < 30.03 < 31.06 < 39.95 g/mol, as if dispersion decided everything. A is the right order read strongest first.

Scan each one for a dissolved ion, then an H on N, O, or F, then polarity. The first test it passes names its strongest force.
Dr. Karmach

Practice 5: the route on the chart

Ar < CH₂O < CH₃NH₂ < Na⁺ in water · answer D
dispersion only · dipole–dipole · hydrogen bonding · ion–dipole

Four substances leave by four exits. Read the exits from right to left for the ranking, weakest first. ✓
Dr. Karmach

Check yourself

  1. Acetone (CH₃COCH₃) is a polar molecule with no O–H, N–H, or F–H bond. Name every intermolecular force it has, then the strongest.
  2. Two nonpolar gases differ only in size. Which has the stronger dispersion force, and why?

Stronger intermolecular forces hold a liquid together more tightly, so more heat is needed to boil it. Ranking these forces is the first step toward predicting which substance boils at the higher temperature.

Dr. Karmach

2 · Properties of Liquids

Explain surface tension, viscosity, capillary action, and vapor pressure from the strength of a liquid's intermolecular forces, read a boiling point at any outside pressure from a vapor-pressure curve, and predict which of two liquids shows more of each.

Dr. Karmach

A paper clip on water

Steel is denser than water, yet a paper clip can rest on a still surface. Insects stand on ponds the same way. The surface holds like a stretched skin.

Dr. Karmach

Gasoline and motor oil

gasoline: chains of 4 to 12 carbons · motor oil: chains of 20 to 50 carbons
both nonpolar: dispersion forces only

Gasoline pours thin, and a spill evaporates in minutes. Motor oil pours slowly, and a drip lasts for weeks. Which one's molecules hold each other more tightly?

Dr. Karmach

Gasoline and motor oil

gasoline: chains of 4 to 12 carbons · motor oil: chains of 20 to 50 carbons
both nonpolar: dispersion forces only

Gasoline pours thin, and a spill evaporates in minutes. Motor oil pours slowly, and a drip lasts for weeks. Which one's molecules hold each other more tightly?
Motor oil: its long chains touch more and tangle.

longer chains → stronger dispersion → tighter hold
tighter hold: slower flow and slower escape
Dr. Karmach

Intermolecular forces set a liquid's behavior

The attractions between molecules control how a liquid acts: how its surface holds, how it flows, and how readily its molecules escape as vapor. Stronger attractions hold the molecules together more tightly.

stronger intermolecular forces → higher surface tension · higher viscosity · lower vapor pressure
one cause, three effects · hydrogen bonding > dipole–dipole > dispersion · dispersion grows with molecular size
memory hook: strong forces hold on
the holding properties rise (surface tension, viscosity) · the escaping one falls (vapor pressure)
Dr. Karmach

Cohesion and adhesion

Cohesion is the attraction between molecules of the same liquid. Adhesion is the attraction between the liquid and a different material it touches. Behavior at any boundary follows from which attraction is stronger.

cohesion: liquid ↔ itself · adhesion: liquid ↔ another surface
a raindrop holds together: cohesion · water wets clean glass: adhesion
Dr. Karmach

Surface tension: an inward pull

A molecule inside the liquid is pulled equally in every direction. A surface molecule has neighbors only beside and below, so the net pull is inward. The tightened surface resists stretching.

stronger forces → tighter surface → higher surface tension
drops pull toward spheres, the shape with the least surface · a light object can rest on the tightened surface
Dr. Karmach

Viscosity: resistance to flow

Flow makes molecules slide past their neighbors. Anything that holds neighbors together slows the slide: stronger forces, longer molecules with more contact, lower temperature.

viscosity rises with stronger forces · longer chains · lower temperature
C₅H₁₂ < C₆H₁₄ < C₇H₁₆ in viscosity · warming a liquid always thins it
Dr. Karmach

Capillary action and the meniscus

Adhesion pulls water up the glass wall and cohesion drags the column along: water climbs, surface dipping in the middle. Mercury coheres more than it adheres to glass: it bulges and stays low.

Dr. Karmach

Vapor pressure: escape balanced by return

In a sealed flask, evaporation and condensation soon run at equal rates and the vapor's pressure holds steady: the vapor pressure. Stronger forces let fewer molecules escape, so it sits lower.

Dr. Karmach

Boiling: vapor pressure meets outside pressure

Vapor pressure climbs as a liquid warms. When it matches the external pressure above the liquid, vapor bubbles form throughout and the liquid boils. At exactly 1 atm, this is the normal boiling point.

boils when vapor pressure = external pressure
high mountain: less pressure above → boils cooler · pressure cooker: more pressure above → boils hotter
memory hook: boiling is a pressure match, not a fixed temperature
water: 100 °C at 1 atm · near 82 °C at 0.50 atm · near 120 °C at 2 atm, inside a pressure cooker
Dr. Karmach

Reading a vapor-pressure curve

A liquid boils where its curve meets the outside-pressure line. On a mountain at 0.50 atm, water boils at 82 °C, so pasta cooks slower.

read across at the outside pressure, then down to the temperature
1.00 atm: ether 35 °C · ethanol 78 °C · water 100 °C · weakest forces, lowest boiling point
Dr. Karmach

The method: boiling at an outside pressure

  1. Put the outside pressure in atm. 760 torr = 1 atm.
  2. Read across, then down. Across to the curve, down to the boiling point.
  3. Subtract the starting temperature. The difference is the warming.

Dr. Karmach

Guided example: water on a mountain

a mountain camp near 4,500 m
given: outside pressure 0.57 atm · water starts at 20 °C · wanted: boiling point, warming before it boils

Climbers heat a pot of water from 20 °C where the air presses at 0.57 atm. At what temperature does it boil, and how many degrees does it warm first?

Read the curve at the camp's pressure, not at 1 atm.

Dr. Karmach

Guided example: solution

a mountain camp near 4,500 m
given: outside pressure 0.57 atm · water starts at 20 °C · wanted: boiling point, warming before it boils

Step 1 · Put the outside pressure in atm

The pressure is already in atm: 0.57 atm. No conversion is needed.

Dr. Karmach

Guided example: solution

a mountain camp near 4,500 m
given: outside pressure 0.57 atm · water starts at 20 °C · wanted: boiling point, warming before it boils
Step 1 · Put the outside pressure in atm Step 2 · Read across, then down
0.57 atm → across to water's curve → down to 85 °C

Water boils at 85 °C at this camp, not at 100 °C.

Dr. Karmach

Guided example: solution

a mountain camp near 4,500 m
given: outside pressure 0.57 atm · water starts at 20 °C · wanted: boiling point, warming before it boils
Step 1 · Put the outside pressure in atm Step 2 · Read across, then down
0.57 atm → across to water's curve → down to 85 °C
Step 3 · Subtract the starting temperature
85 °C − 20 °C = 65 °C of warming before it boils
Dr. Karmach

Guided example: solution

a mountain camp near 4,500 m
given: outside pressure 0.57 atm · water starts at 20 °C · wanted: boiling point, warming before it boils
Step 1 · Put the outside pressure in atm Step 2 · Read across, then down
0.57 atm → across to water's curve → down to 85 °C
Step 3 · Subtract the starting temperature
85 °C − 20 °C = 65 °C of warming before it boils
Water boils 15 °C below its normal 100 °C at this camp, so the pot warms 65 °C, not 80 °C. The cooler boiling water cooks food more slowly. ✓
Dr. Karmach

Guided example: the route on the map

given: 0.57 atm · water starts at 20 °C
found: boils at 85 °C · warms 65 °C before it boils

The pressure came in atm, so the ÷ 760 branch stays dark: read the curve, then subtract the start. ✓
Dr. Karmach

The method: comparing two liquids

  1. Identify each liquid's strongest force. Hydrogen bonding, dipole–dipole, or dispersion; same type, then size decides.
  2. Name what the property measures. Holding a surface, flowing, or escaping.
  3. Stronger forces hold tighter. More surface tension, more viscosity, less vapor.

Dr. Karmach

Worked example 1: viscosity of two liquids

hexane (C₆H₁₄) vs 1-pentanol (C₅H₁₁OH)
86.17 g/mol · 88.15 g/mol · nearly equal size · wanted: the more viscous liquid

Two clear liquids of nearly the same molar mass. One pours like water; the other pours like a light oil.

Name the more viscous liquid, and the force that explains it.

Dr. Karmach

Worked example 1: solution

hexane (C₆H₁₄) vs 1-pentanol (C₅H₁₁OH)
86.17 g/mol · 88.15 g/mol · nearly equal size

Step 1 · Identify each liquid's strongest force

Hexane is a nonpolar hydrocarbon: dispersion only. 1-Pentanol carries an O–H, so it hydrogen bonds. Nearly equal size means nearly equal dispersion; the O–H is the difference.

Dr. Karmach

Worked example 1: solution

hexane (C₆H₁₄) vs 1-pentanol (C₅H₁₁OH)
86.17 g/mol · 88.15 g/mol · nearly equal size
Step 1 · Identify each liquid's strongest force Step 2 · Name what the property measures

Viscosity measures resistance to flow. To flow, each molecule must slide past its neighbors, and sliding means briefly pulling away from them.

Dr. Karmach

Worked example 1: solution

hexane (C₆H₁₄) vs 1-pentanol (C₅H₁₁OH)
86.17 g/mol · 88.15 g/mol · nearly equal size
Step 1 · Identify each liquid's strongest force Step 2 · Name what the property measures Step 3 · Stronger forces hold tighter
1-pentanol: hydrogen bonding vs hexane: dispersion → 1-pentanol is more viscous
Dr. Karmach

Worked example 1: solution

hexane (C₆H₁₄) vs 1-pentanol (C₅H₁₁OH)
86.17 g/mol · 88.15 g/mol · nearly equal size
Step 1 · Identify each liquid's strongest force Step 2 · Name what the property measures Step 3 · Stronger forces hold tighter
1-pentanol: hydrogen bonding vs hexane: dispersion → 1-pentanol is more viscous
Near room temperature 1-pentanol is about twelve times as viscous as hexane, at nearly the same molar mass. The hydrogen bonds make the difference. ✓
Dr. Karmach

Worked example 1: the route on the strip

hexane (C₆H₁₄) vs 1-pentanol (C₅H₁₁OH)
viscosity measures holding on · found: 1-pentanol is more viscous

A holding property rises with the stronger force. Hydrogen bonding beats dispersion, so 1-pentanol flows more slowly. ✓
Dr. Karmach

Worked example 2: vapor pressure in sealed flasks

diethyl ether (C₂H₅OC₂H₅) vs water (H₂O), sealed flasks at 20 °C
74.12 g/mol · 18.02 g/mol · wanted: the higher vapor pressure

Neither flask is anywhere near boiling.

A common first answer: neither shows a vapor pressure, because neither liquid is boiling.

Name the liquid with the higher vapor pressure.

Dr. Karmach

Worked example 2: solution

diethyl ether (C₂H₅OC₂H₅) vs water (H₂O), sealed flasks at 20 °C
74.12 g/mol · 18.02 g/mol

The common first answer, tested

Sealed above any liquid, at any temperature, some molecules escape while others return. Both flasks hold vapor at a steady pressure, so both liquids show a vapor pressure. Boiling is not required.

Dr. Karmach

Worked example 2: solution

diethyl ether (C₂H₅OC₂H₅) vs water (H₂O), sealed flasks at 20 °C
74.12 g/mol · 18.02 g/mol
The common first answer, tested Step 1 · Identify each liquid's strongest force

Water hydrogen bonds through its O–H. Diethyl ether is polar, but every H sits on carbon: ordinary dipole–dipole, far weaker.

Dr. Karmach

Worked example 2: solution

diethyl ether (C₂H₅OC₂H₅) vs water (H₂O), sealed flasks at 20 °C
74.12 g/mol · 18.02 g/mol
The common first answer, tested Step 1 · Identify each liquid's strongest force Step 2 · Name what the property measures

Vapor pressure measures escape: how much vapor builds before condensation catches up with evaporation.

Dr. Karmach

Worked example 2: solution

diethyl ether (C₂H₅OC₂H₅) vs water (H₂O), sealed flasks at 20 °C
74.12 g/mol · 18.02 g/mol
The common first answer, tested Step 1 · Identify each liquid's strongest force Step 2 · Name what the property measures Step 3 · Stronger forces hold tighter
ether: weaker forces → more molecules escape → diethyl ether has the higher vapor pressure
Dr. Karmach

Worked example 2: solution

diethyl ether (C₂H₅OC₂H₅) vs water (H₂O), sealed flasks at 20 °C
74.12 g/mol · 18.02 g/mol
The common first answer, tested Step 1 · Identify each liquid's strongest force Step 2 · Name what the property measures Step 3 · Stronger forces hold tighter
ether: weaker forces → more molecules escape → diethyl ether has the higher vapor pressure
At 20 °C, ether's vapor pressure is about 25 times water's: 442 torr against 17.5 torr. Weak forces, easy escape, high vapor pressure. ✓
Dr. Karmach

Worked example 2: the route on the strip

diethyl ether (C₂H₅OC₂H₅) vs water (H₂O), sealed flasks at 20 °C
vapor pressure measures escape · found: diethyl ether has the higher vapor pressure

An escaping property falls with the stronger force. Water's hydrogen bonds hold its molecules back, so ether's vapor pressure is the higher one. ✓
Dr. Karmach

Take-home: every liquid has a vapor pressure

Boiling is not required. Above any liquid in a closed space, escape and return balance at a steady vapor pressure. Warmer liquid, more molecules with escape energy, higher vapor pressure.

any liquid, any temperature → some vapor pressure
higher temperature → higher vapor pressure · stronger forces → lower vapor pressure at the same temperature
Dr. Karmach

Your turn: surface tension

water (H₂O) vs acetone (CH₃COCH₃)
18.02 g/mol · 58.08 g/mol · wanted: the higher surface tension
step comparison
1 · strongest force water: · acetone:
2 · what the property measures resistance to stretching the
3 · stronger forces hold tighter higher surface tension:

Fill the blanks. Acetone is the heavier molecule; watch which force each liquid can use.

Dr. Karmach

Your turn: surface tension

water (H₂O) vs acetone (CH₃COCH₃)
18.02 g/mol · 58.08 g/mol · wanted: the higher surface tension
step comparison
1 · strongest force water: · acetone:
2 · what the property measures resistance to stretching the
3 · stronger forces hold tighter higher surface tension:
water → higher surface tension
water: hydrogen bonding · acetone: dipole–dipole (no O–H) · water's surface pulls inward roughly three times harder
Force type outranks size: water's hydrogen bonds tighten its surface far more than acetone's dipoles can. ✓
Dr. Karmach

Where this goes wrong

Treating viscosity as density. Motor oil floats on water: it is less dense. Yet oil pours far more slowly: it is more viscous. Density is mass per volume; viscosity is resistance to flow. A liquid can be light and thick at the same time.
Waiting for boiling before vapor pressure. Every liquid has a vapor pressure at every temperature; a sealed bottle of water on a shelf holds vapor at its steady pressure. Boiling is the special temperature where the vapor pressure climbs to match the pressure outside.
Making stronger forces raise everything. Stronger forces raise surface tension and viscosity but lower vapor pressure. The first two measure how well molecules hold on; vapor pressure measures how easily they escape. One cause, opposite directions.
Expecting every liquid to curve like water. The meniscus reports a contest. Adhesion to glass beats cohesion in water: concave, and the liquid climbs. Cohesion beats adhesion in mercury: convex, and the level sits low.
Dr. Karmach

Practice 1: boiling below sea level

the floor of Death Valley: 86 m below sea level
at sea level: 1.00 atm · water's normal boiling point: 100 °C

How does water's boiling point on the valley floor compare with 100 °C?

  1. Lower: the air pressure there is below 1 atm
  2. The same: water always boils at 100 °C
  3. Higher: the air pressure there is above 1 atm
  4. Higher: water's hydrogen bonds are stronger there
Dr. Karmach

Practice 1 answer: C

below sea level → more air above → outside pressure above 1 atm → boils above 100 °C · answer C
boils when vapor pressure = outside pressure · about 1.01 atm on the valley floor · water boils near 100.3 °C

A reversed the direction: air pressure falls going up a mountain and rises going below sea level. B treated the boiling point as fixed; 100 °C holds only at exactly 1 atm. D changed the forces; water's hydrogen bonds are the same everywhere, and only the pressure it must match changes.

86 m adds only a little air, so water boils only slightly above 100 °C. More pressure above, hotter boil. ✓
Dr. Karmach

Practice 2: reading a vapor-pressure curve

From the curves, what are propane's normal boiling point and its boiling point at 0.40 atm, in °C?

  1. normal −42, at 0.40 atm −61
  2. normal −61, at 0.40 atm −42
  3. normal −42, at 0.40 atm −42
  4. normal −1, at 0.40 atm −23
Dr. Karmach

Practice 2 answer: A

1.00 atm line meets propane at −42 °C · 0.40 atm line meets it at −61 °C · answer A
read across at the outside pressure, then down to the temperature · less pressure above → boils cooler

B swaps the reads: a lower outside pressure pairs with the lower temperature, never the higher one. C read the 1.00 atm line twice, as if a boiling point were fixed. D read butane's curve, the one on the right.

Propane boils 19 °C cooler at 0.40 atm, the same direction as water on a mountain. ✓
Dr. Karmach

Practice 2: the route on the curve

propane: across at 1.00 atm, down to −42 °C · across at 0.40 atm, down to −61 °C
both pressures given in atm · no starting temperature, so nothing to subtract

Two reads on one curve. The lower outside pressure meets propane's curve at the cooler temperature. ✓
Dr. Karmach

Practice 3

an unknown liquid in a clean, narrow glass tube
the surface bulges upward (convex) · the level in the tube sits below the level outside

A clean glass capillary tube is dipped into a liquid. The liquid's surface bulges upward, and it does not climb. What does this show?

  1. Cohesion within the liquid is stronger than its adhesion to the glass
  2. Adhesion to the glass is stronger than cohesion within the liquid
  3. The glass repels the liquid, pushing its surface into a dome
  4. The liquid has no intermolecular forces, so nothing pulls it up the wall
Dr. Karmach

Practice 3 answer: A

convex meniscus, no climb → cohesion > adhesion · answer A
the liquid's own attractions beat its attraction to the wall · mercury in glass behaves this way

B describes water: when adhesion wins, the edge is dragged up the wall, giving a concave dip and a climbing column. C invents a repulsion; glass attracts every liquid at least weakly, and the dome comes from the liquid's own inward pull. D cannot happen: every substance has at least dispersion forces.

A dip in the middle means adhesion leads; a bulge means cohesion leads. The shape reads out the force balance directly.
Dr. Karmach

Practice 4

1-propanol (C₃H₇OH) · acetone (CH₃COCH₃) · pentane (C₅H₁₂), sealed flasks at 20 °C
60.09 g/mol · 58.08 g/mol · 72.15 g/mol

Rank the three liquids from lowest to highest vapor pressure.

  1. pentane < acetone < 1-propanol
  2. 1-propanol < acetone < pentane
  3. pentane < 1-propanol < acetone
  4. 1-propanol < pentane < acetone
Dr. Karmach

Practice 4 answer: B

1-propanol < acetone < pentane · answer B
hydrogen bonding · dipole–dipole · dispersion only · weaker forces, more escape

The masses sit close, so force type decides. 1-Propanol's O–H hydrogen bonds. Acetone is polar with no O–H. Pentane is nonpolar. Vapor pressure measures escape, so it rises as the forces weaken.

A ranked the attractions, not the vapor pressure; stronger forces lower it. C ranked by molar mass alone, but pentane's extra mass cannot outpull a dipole or a hydrogen bond. D read acetone as nonpolar; its C=O makes it polar, so it holds on harder than pentane.

Strong forces hold, weak forces let go. Vapor pressure climbs from the hydrogen-bonded liquid to the dispersion-only one.
Dr. Karmach

Practice 5: inside a pressure cooker

a sealed pressure cooker on the stove
given: 1270 torr above the water · water at 22 °C when the lid locks

The lid keeps 1270 torr over water that starts at 22 °C. By how many degrees Celsius does it warm before it boils?

  1. 115
  2. 78
  3. 100
  4. 93
Dr. Karmach

Practice 5 answer: D

pressure cooker: 1270 torr above the water · water starts at 22 °C
three moves: torr to atm · read the curve · subtract the start
1270 torr × 1 atm760 torr = 1.67 atm → curve: boils at 115 °C
Dr. Karmach

Practice 5 answer: D

pressure cooker: 1270 torr above the water · water starts at 22 °C
three moves: torr to atm · read the curve · subtract the start
1270 torr × 1 atm760 torr = 1.67 atm → curve: boils at 115 °C
115 °C − 22 °C = 93 °C of warming (answer D)

A stopped at the boiling point: 115 is where the water boils, not how far it warms. B used the normal boiling point: 100 − 22 = 78. C gave the normal boiling point itself, 100, a temperature and not a change.

Dr. Karmach

Practice 5 answer: D

pressure cooker: 1270 torr above the water · water starts at 22 °C
three moves: torr to atm · read the curve · subtract the start
1270 torr × 1 atm760 torr = 1.67 atm → curve: boils at 115 °C
115 °C − 22 °C = 93 °C of warming (answer D)
More pressure above, hotter boil: 115 °C instead of 100 °C, so food cooks faster. ✓
Dr. Karmach

Practice 5: the route on the map

given: 1270 torr · water starts at 22 °C
found: 1.67 atm · boils at 115 °C · warms 93 °C before it boils

The pressure came in torr, so this route runs through ÷ 760 before the curve, then subtracts the start. ✓
Dr. Karmach

Check yourself

  1. Glycerol's molecules each carry three O–H groups; acetone's carry none. Which liquid is more viscous at room temperature, and why?
  2. A sealed flask of water sits at a steady vapor pressure. Name the two processes still running at the liquid surface and compare their rates.

A liquid boils when its vapor pressure climbs to meet the pressure above it. Stronger intermolecular forces mean a lower vapor pressure, so more heat is needed: ranking forces predicts which liquid boils higher.

Dr. Karmach

3 · IMFs & Boiling Point

Predict which substance boils higher from its intermolecular forces: the stronger the attraction between molecules, the more energy needed to pull them apart, so the higher the boiling point; among nonpolar molecules the bigger one disperses more.

Dr. Karmach

Three liquids off your skin

Rubbing alcohol dries in seconds. Water lingers for minutes. Cooking oil barely leaves at all. Stronger attractions between molecules hold a liquid together longer.

Dr. Karmach

Boiling pulls molecules apart

To boil, molecules must break free of their neighbors, and stronger attractions take more energy to overcome. The stronger the intermolecular forces, the higher the boiling point.

stronger intermolecular forces → higher boiling point
also raises melting point, surface tension, viscosity · lowers vapor pressure
Dr. Karmach

Boiling points compare the forces

water boils at 100 °C · rubbing alcohol boils at 82 °C
both at 1 atm · to boil, molecules must pull free of their neighbors

Which liquid's molecules attract each other more strongly?

Dr. Karmach

Boiling points compare the forces

water boils at 100 °C · rubbing alcohol boils at 82 °C
both at 1 atm · to boil, molecules must pull free of their neighbors

Which liquid's molecules attract each other more strongly?
Water. It must be heated 18 °C further before its molecules break free. A higher boiling point means stronger intermolecular forces.

Dr. Karmach

Ranking the forces at equal size

When molecules are about the same size, the type of force sets the order. Hydrogen bonding pulls hardest, ordinary dipole–dipole attraction is weaker, and dispersion is weakest of the three.

at ≈ 44–46 g/mol: ethanol (hydrogen bonding) 78 °C · dimethyl ether (dipole–dipole) −24 °C · propane (dispersion) −42 °C
nearly equal mass, so dispersion is nearly equal · the stronger force type boils higher
memory hook: type first, size breaks the tie
compare force types first · only within one type does the bigger molecule win
Dr. Karmach

Bigger nonpolar molecules boil higher

Nonpolar molecules have only dispersion forces. Dispersion comes from the electrons, so a bigger molecule with more electrons and more surface attracts more strongly.

Dr. Karmach

The method

  1. Identify each substance's strongest force. Hydrogen bonding, dipole–dipole, or dispersion.
  2. The stronger force boils higher. Across types, rank them: hydrogen bonding > dipole–dipole > dispersion.
  3. For a tie, the bigger molecule attracts more. Same type: more electrons, more surface.

Dr. Karmach

Guided example: nitrogen and carbon monoxide

nitrogen (N₂) vs carbon monoxide (CO)
N₂ 28.02 g/mol · CO 28.01 g/mol · wanted: which boils higher, and why

Two gases with the same molar mass, so dispersion is the same for both. Nitrogen joins two identical atoms; carbon monoxide joins two different ones.

Name the higher-boiling gas, and the force that explains it.

Dr. Karmach

Guided example: solution

nitrogen (N₂) vs carbon monoxide (CO)
N₂ 28.02 g/mol · CO 28.01 g/mol

Step 1 · Identify each substance's strongest force

N₂ joins two identical atoms, so it is nonpolar: dispersion only. CO joins carbon to oxygen, which pull on the shared electrons unequally, so CO is polar: dipole–dipole.

Dr. Karmach

Guided example: solution

nitrogen (N₂) vs carbon monoxide (CO)
N₂ 28.02 g/mol · CO 28.01 g/mol
Step 1 · Identify each substance's strongest force Step 2 · The stronger force boils higher

The types differ, so the type decides. Dipole–dipole is stronger than dispersion alone, so CO boils higher.

CO −191.5 °C · N₂ −195.8 °C
dipole–dipole vs dispersion · 28.01 vs 28.02 g/mol
Dr. Karmach

Guided example: solution

nitrogen (N₂) vs carbon monoxide (CO)
N₂ 28.02 g/mol · CO 28.01 g/mol
Step 1 · Identify each substance's strongest force Step 2 · The stronger force boils higher
CO −191.5 °C · N₂ −195.8 °C
dipole–dipole vs dispersion · 28.01 vs 28.02 g/mol
CO boils 4.3 °C higher. A weak dipole gives a small lift, but the order follows the force type. ✓
Dr. Karmach

Guided example: the route on the map

nitrogen (N₂) vs carbon monoxide (CO)
given: 28.02 vs 28.01 g/mol · found: CO boils higher, −191.5 °C vs −195.8 °C

Two different force types, so only the top row was used. The masses match, so size never entered. ✓
Dr. Karmach

Practice 1

hydrogen fluoride (HF) vs hydrogen chloride (HCl)
HF 20.01 g/mol · HCl 36.46 g/mol · both polar molecules

Which has the higher boiling point?

  1. HCl: the heavier molecule has more dispersion
  2. HF: its H on F adds hydrogen bonding
  3. Neither: both are polar, so they boil near the same temperature
  4. HCl: its H on Cl adds hydrogen bonding
Dr. Karmach

Practice 1 answer: B

HF: hydrogen bonding · HCl: dipole–dipole · answer B
H on F qualifies · H on Cl does not · HF 20 °C vs HCl −85 °C

A ranked by mass alone; the force type comes first, and HF has the stronger type. C stopped at dipole–dipole; the H on F adds hydrogen bonding on top. D let chlorine qualify; only N, O, or F do.

HF boils 105 °C above HCl at about half its mass. Type first. ✓
Dr. Karmach

Practice 1 answer: B

HF: hydrogen bonding · HCl: dipole–dipole · answer B
H on F qualifies · H on Cl does not · HF 20 °C vs HCl −85 °C
HF boils 105 °C above HCl at about half its mass. Type first. ✓
The route on the map

Dr. Karmach

Worked example 1: same size, different force

dimethyl ether (CH₃OCH₃) vs ethanol (C₂H₅OH)
both C₂H₆O, molar mass 46.07 g/mol · wanted: which boils higher, and why

Two liquids built from the same atoms: the same molar mass, and nearly the same dispersion.

Name the higher-boiling liquid, and the force that explains it.

Dr. Karmach

Worked example 1: solution

dimethyl ether (CH₃OCH₃) vs ethanol (C₂H₅OH)
both C₂H₆O, 46.07 g/mol

Step 1 · Identify each substance's strongest force

Ethanol has an O–H bond, so it hydrogen bonds. Dimethyl ether is polar but has no O–H, so its strongest force is ordinary dipole–dipole attraction.

Dr. Karmach

Worked example 1: solution

dimethyl ether (CH₃OCH₃) vs ethanol (C₂H₅OH)
both C₂H₆O, 46.07 g/mol
Step 1 · Identify each substance's strongest force Step 2 · The stronger force boils higher

Equal molar mass means dispersion is the same for both, so only the force type differs. Hydrogen bonding is stronger than dipole–dipole, so ethanol boils higher.

ethanol 78 °C · dimethyl ether −24 °C
hydrogen bonding vs dipole–dipole · same 46.07 g/mol
Dr. Karmach

Worked example 1: solution

dimethyl ether (CH₃OCH₃) vs ethanol (C₂H₅OH)
both C₂H₆O, 46.07 g/mol
Step 1 · Identify each substance's strongest force Step 2 · The stronger force boils higher
ethanol 78 °C · dimethyl ether −24 °C
hydrogen bonding vs dipole–dipole · same 46.07 g/mol
Identical mass, and hydrogen bonding lifts ethanol's boiling point 102 °C above dimethyl ether's. The force type, not the size, made the difference. ✓
Dr. Karmach

Worked example 1: the route on the map

dimethyl ether (CH₃OCH₃) vs ethanol (C₂H₅OH)
given: both 46.07 g/mol · found: ethanol boils higher, 78 °C vs −24 °C

Hydrogen bonding against dipole–dipole: two different types, so the top row settles it. ✓
Dr. Karmach

Worked example 2: two halogens

chlorine (Cl₂) vs iodine (I₂)
Cl₂ 70.90 g/mol · I₂ 253.80 g/mol · both nonpolar · wanted: which boils higher, and why

A common first answer: both are nonpolar molecules with only dispersion forces, so they should boil at about the same temperature.

Name the higher-boiling halogen, and the reason.

Dr. Karmach

Worked example 2: solution

chlorine (Cl₂) vs iodine (I₂)
Cl₂ 70.90 g/mol · I₂ 253.80 g/mol · both nonpolar

Step 1 · Identify each substance's strongest force

Both are nonpolar, so dispersion is the only force acting in each.

Dr. Karmach

Worked example 2: solution

chlorine (Cl₂) vs iodine (I₂)
Cl₂ 70.90 g/mol · I₂ 253.80 g/mol · both nonpolar
Step 1 · Identify each substance's strongest force Step 2 · The stronger force boils higher

Same force type does not mean same strength. The molecule held by stronger dispersion boils higher.

Dr. Karmach

Worked example 2: solution

chlorine (Cl₂) vs iodine (I₂)
Cl₂ 70.90 g/mol · I₂ 253.80 g/mol · both nonpolar
Step 1 · Identify each substance's strongest force Step 2 · The stronger force boils higher Step 3 · For a tie, the bigger molecule attracts more

Iodine is far larger than chlorine, with many more electrons, so its dispersion is much stronger. Iodine boils higher.

iodine 184 °C · chlorine −34 °C
253.80 g/mol vs 70.90 g/mol · dispersion grows with size
Dr. Karmach

Worked example 2: solution

chlorine (Cl₂) vs iodine (I₂)
Cl₂ 70.90 g/mol · I₂ 253.80 g/mol · both nonpolar
Step 1 · Identify each substance's strongest force Step 2 · The stronger force boils higher Step 3 · For a tie, the bigger molecule attracts more
iodine 184 °C · chlorine −34 °C
253.80 g/mol vs 70.90 g/mol · dispersion grows with size
Iodine boils 218 °C above chlorine, and at room temperature iodine is a solid while chlorine is a gas. Same force type, very different strength. ✓
Dr. Karmach

Worked example 2: the route on the map

chlorine (Cl₂) vs iodine (I₂)
given: 70.90 vs 253.80 g/mol · found: iodine boils higher, 184 °C vs −34 °C

Both have only dispersion, a tie in type, so the bottom row settles it: the bigger molecule boils higher. ✓
Dr. Karmach

Take-home: type outranks mass

Size decides only among one force type. Across types, the stronger force wins against a far heavier molecule. Tin hydride is nearly seven times water's mass, yet water boils higher because water hydrogen bonds.

Dr. Karmach

Your turn: methanol and ethane

methanol (CH₃OH) 32.04 g/mol · ethane (C₂H₆) 30.07 g/mol
nearly equal mass, so dispersion is nearly equal
methanol: strongest force = · ethane: strongest force = · higher boiling point:

Fill each strongest force, then name the higher-boiling liquid.

Dr. Karmach

Your turn: methanol and ethane

methanol (CH₃OH) 32.04 g/mol · ethane (C₂H₆) 30.07 g/mol
nearly equal mass, so dispersion is nearly equal
methanol: strongest force = · ethane: strongest force = · higher boiling point:

Fill each strongest force, then name the higher-boiling liquid.

methanol: hydrogen bonding (O–H) · ethane: dispersion (nonpolar) · higher boiling point: methanol
Equal mass, so dispersion ties. Methanol's O–H adds hydrogen bonding, and it boils at 65 °C against ethane's −89 °C, 154 °C higher. ✓
Dr. Karmach

Where this goes wrong

Heavier always boils higher. Mass alone does not decide. Water, 18.02 g/mol, boils at 100 °C, above butane at 58.12 g/mol (−0.5 °C), because water hydrogen bonds while butane has only dispersion. Rank by force first; size counts only within one type.
Reversing the trend. "Lighter molecules move faster, so they need a higher temperature to boil." Weakly held molecules escape more easily, not less. Weak forces mean a low boiling point; strong forces mean a high one.
Confusing forces with bonds. "The bigger molecule boils higher because its covalent bonds are stronger." Boiling never breaks the covalent bonds inside a molecule. It overcomes the attractions between whole molecules, which are far weaker than bonds.
Same type, same boiling point. Two nonpolar molecules share the dispersion force but not its strength. Dispersion grows with size, so iodine (253.80 g/mol) boils far above chlorine (70.90 g/mol).
Dr. Karmach

Practice 2

pentane (C₅H₁₂) vs heptane (C₇H₁₆)
pentane 72.15 g/mol · heptane 100.20 g/mol · both nonpolar

Pentane and heptane are both nonpolar. Which boils at the higher temperature, and why?

  1. Heptane: it is the larger molecule, so its dispersion forces are stronger and take more energy to overcome.
  2. Heptane: its covalent bonds are stronger and must be broken for it to boil.
  3. Pentane: lighter molecules move faster, so a higher temperature is needed to boil them off.
  4. They boil at nearly the same temperature, since both are nonpolar and rely on the same force.
Dr. Karmach

Practice 2 answer: A

pentane (C₅H₁₂) vs heptane (C₇H₁₆)
pentane 72.15 g/mol · heptane 100.20 g/mol · both nonpolar: dispersion only

Both are nonpolar, so dispersion is the only force. Heptane is the larger molecule, so its dispersion is stronger and it boils higher. Answer A.

B confused forces with bonds: boiling overcomes the attractions between molecules, never the covalent bonds inside them. C reversed the trend: weakly held light molecules escape more easily and boil lower, not higher. D forgot that the same force type can differ in strength, and dispersion grows with size.

Heptane boils at 98 °C, pentane at 36 °C, 62 °C higher for the larger molecule. ✓
Dr. Karmach

Practice 2 answer: A

pentane (C₅H₁₂) vs heptane (C₇H₁₆)
pentane 72.15 g/mol · heptane 100.20 g/mol · both nonpolar: dispersion only
Heptane boils at 98 °C, pentane at 36 °C, 62 °C higher for the larger molecule. ✓
The route on the map

Dr. Karmach

Practice 3

hydrogen chloride (HCl) vs hydrogen bromide (HBr)
HCl 36.46 g/mol · HBr 80.91 g/mol · both polar · HCl is the more polar molecule

Which boils higher, and why?

  1. HCl: its larger dipole gives stronger dipole–dipole attraction
  2. HBr: the H on Br adds hydrogen bonding
  3. HBr: the larger molecule has stronger dispersion
  4. HCl: the H on Cl adds hydrogen bonding
Dr. Karmach

Practice 3 answer: C

HCl and HBr: both dipole–dipole, a tie in type · answer C
the bigger molecule breaks the tie · HBr 80.91 vs HCl 36.46 g/mol · HBr −67 °C vs HCl −85 °C

A let polarity decide inside a tie; with the type tied, size decides, and HBr's much larger electron cloud outweighs HCl's slightly larger dipole. B and D let Br or Cl qualify for hydrogen bonding; only N, O, or F do.

HBr boils 18 °C above HCl, though HCl is the more polar molecule. ✓
Dr. Karmach

Practice 3 answer: C

HCl and HBr: both dipole–dipole, a tie in type · answer C
the bigger molecule breaks the tie · HBr 80.91 vs HCl 36.46 g/mol · HBr −67 °C vs HCl −85 °C
HBr boils 18 °C above HCl, though HCl is the more polar molecule. ✓
The route on the map

Dr. Karmach

Worked example 3: rank three by boiling point

butane (C₄H₁₀) · acetone (C₃H₆O) · 1-propanol (C₃H₈O)
58.12 · 58.08 · 60.09 g/mol · nearly equal mass · wanted: order the boiling points

Three liquids of nearly equal molar mass, so dispersion is about the same for all three.

Rank the three boiling points from lowest to highest.

Dr. Karmach

Worked example 3: solution

butane (C₄H₁₀) · acetone (C₃H₆O) · 1-propanol (C₃H₈O)
58.12 · 58.08 · 60.09 g/mol · nearly equal mass

Step 1 · Identify each substance's strongest force

Butane is nonpolar: dispersion only. Acetone is polar with no O–H: dipole–dipole. 1-Propanol has an O–H: hydrogen bonding.

Dr. Karmach

Worked example 3: solution

butane (C₄H₁₀) · acetone (C₃H₆O) · 1-propanol (C₃H₈O)
58.12 · 58.08 · 60.09 g/mol · nearly equal mass
Step 1 · Identify each substance's strongest force Step 2 · The stronger force boils higher

Mass is nearly equal, so dispersion ties and the force type sets the order. Hydrogen bonding beats dipole–dipole beats dispersion, so 1-propanol > acetone > butane.

butane −0.5 °C · acetone 56 °C · 1-propanol 97 °C
dispersion < dipole–dipole < hydrogen bonding · masses within 2 g/mol
Dr. Karmach

Worked example 3: solution

butane (C₄H₁₀) · acetone (C₃H₆O) · 1-propanol (C₃H₈O)
58.12 · 58.08 · 60.09 g/mol · nearly equal mass
Step 1 · Identify each substance's strongest force Step 2 · The stronger force boils higher
butane −0.5 °C · acetone 56 °C · 1-propanol 97 °C
dispersion < dipole–dipole < hydrogen bonding · masses within 2 g/mol
Lowest to highest: butane −0.5 °C, acetone 56 °C, 1-propanol 97 °C. Propanol boils 41 °C above acetone on hydrogen bonding alone, at nearly the same mass. ✓
Dr. Karmach

Worked example 3: the route on the map

butane (C₄H₁₀) · acetone (C₃H₆O) · 1-propanol (C₃H₈O)
given: 58.12 · 58.08 · 60.09 g/mol · found: butane −0.5 °C · acetone 56 °C · 1-propanol 97 °C

Three different types at nearly equal mass: the top row alone sets the whole order. ✓
Dr. Karmach

Practice 4

neon (Ne) · krypton (Kr) · phosphine (PH₃) · ammonia (NH₃)
20.18 · 83.80 · 34.00 · 17.03 g/mol · PH₃ and NH₃ are polar molecules

Rank the four substances from lowest to highest boiling point.

  1. NH₃ < Ne < PH₃ < Kr
  2. Ne < Kr < NH₃ < PH₃
  3. Kr < Ne < PH₃ < NH₃
  4. Ne < Kr < PH₃ < NH₃
Dr. Karmach

Practice 4 answer: D

Ne < Kr < PH₃ < NH₃ · answer D
dispersion · dispersion, larger atom · dipole–dipole · hydrogen bonding

Neon and krypton are nonpolar atoms: dispersion only, and the larger krypton attracts more. PH₃ is polar, but its H sits on P: dipole–dipole. NH₃ has H on N: hydrogen bonding.

A ranked by mass alone; krypton is the heaviest, yet it has only dispersion. B let PH₃ hydrogen bond, but an H on P does not qualify. C reversed the size tie; the bigger atom disperses more and boils higher.

Measured: Ne −246 °C, Kr −153 °C, PH₃ −88 °C, NH₃ −33 °C. Type first, then size breaks the tie. ✓
Dr. Karmach

Practice 4 answer: D

Ne < Kr < PH₃ < NH₃ · answer D
dispersion · dispersion, larger atom · dipole–dipole · hydrogen bonding
Measured: Ne −246 °C, Kr −153 °C, PH₃ −88 °C, NH₃ −33 °C. Type first, then size breaks the tie. ✓
The route on the map

Dr. Karmach

More O–H groups, more hydrogen bonds

1-propanol (CH₃CH₂CH₂OH) 97 °C · ethylene glycol (HOCH₂CH₂OH) 197 °C
60.09 vs 62.07 g/mol · one O–H vs two · both hydrogen bond

Both hydrogen bond, at nearly the same mass. Each O–H group is one more site for hydrogen bonds, so two O–H groups hold far tighter. Ethylene glycol boils 100 °C higher.

Dr. Karmach

Practice 5

CS₂ · butanone (CH₃COCH₂CH₃) · 1-butanol (CH₃CH₂CH₂CH₂OH) · propylene glycol (CH₃CH(OH)CH₂OH)
76.13 · 72.10 · 74.12 · 76.09 g/mol

Rank the four from lowest to highest boiling point.

  1. butanone < 1-butanol < propylene glycol < CS₂
  2. CS₂ < butanone < propylene glycol < 1-butanol
  3. propylene glycol < 1-butanol < butanone < CS₂
  4. butanone < CS₂ < 1-butanol < propylene glycol
  5. CS₂ < butanone < 1-butanol < propylene glycol
Dr. Karmach

Practice 5 answer: E

CS₂ < butanone < 1-butanol < propylene glycol · answer E
dispersion · dipole–dipole · hydrogen bonding, one O–H · hydrogen bonding, two O–H

A ranked by molar mass alone; all four sit within 4.03 g/mol, so the force type decides. B ranked the two alcohols by chain length; the second O–H outweighs one extra carbon. C is the right order read highest first. D read butanone as nonpolar; its C=O makes it polar, like acetone.

Measured: CS₂ 46 °C, butanone 80 °C, 1-butanol 118 °C, propylene glycol 188 °C. Type first, then count the O–H groups. ✓
Dr. Karmach

Practice 5 answer: E

CS₂ < butanone < 1-butanol < propylene glycol · answer E
dispersion · dipole–dipole · hydrogen bonding, one O–H · hydrogen bonding, two O–H
Measured: CS₂ 46 °C, butanone 80 °C, 1-butanol 118 °C, propylene glycol 188 °C. Type first, then count the O–H groups. ✓
The route on the map

Dr. Karmach

Check yourself

  1. Neon and argon are both nonpolar. Which boils at the higher temperature, and which force decides it?
  2. Dimethyl ether and ethanol have the same molar mass. Which boils higher, and why?

The strength ranking you just built predicts which substances give up their liquid state easily and which hold on. Mapping when a substance melts, boils, or sublimes under any pressure comes next: the phase diagram.

Dr. Karmach

4 · Phase Diagrams

Read a pressure–temperature phase diagram: name the stable phase at any P,T, follow a constant-pressure or constant-temperature path and list the phase changes, and locate the triple point, critical point, and the normal melting and boiling points on the 1-atm line.

Dr. Karmach

One map for all three states

Water can be ice, liquid, or steam. A phase diagram is the single map that says which one you get, for any pressure and temperature you choose.

Dr. Karmach

The vapor-pressure curve is a border

a liquid boils when its vapor pressure = the outside pressure
water: vapor pressure 101.3 kPa = 1 atm at 100 °C → the normal boiling point

Every point on the curve is a temperature and pressure where liquid and gas coexist. Above it, water stays liquid; below it, gas. A phase diagram draws this border and two more.

Dr. Karmach

A phase diagram maps pressure vs temperature

A phase diagram plots pressure (y) against temperature (x) for one pure substance. Every point is one P,T pair. The region the point lands in names the stable phase: solid, liquid, or gas.

pick a pressure and a temperature → read off the stable phase
x-axis = Temperature · y-axis = Pressure · each point names one phase of one pure substance
Dr. Karmach

Three regions, three dividing curves

Three regions are separated by three curves. On a curve two phases coexist, so crossing a curve is a phase change.

memory hook: each curve is named for the change across it
fusion: solid | liquid · vaporization: liquid | gas · sublimation: solid | gas
Dr. Karmach

Two special points

triple point: the one P,T where solid, liquid, and gas all coexist
the single spot where all three curves meet
critical point (Tc, Pc): the top end of the vaporization curve
beyond it the liquid–gas boundary disappears → a supercritical fluid, neither true liquid nor gas

Above the critical temperature, no amount of pressure makes a separate liquid.

memory hook: triple means three phases meet · critical means the liquid–gas line ends
triple point sits low and left · critical point sits at the top of the vaporization curve
Dr. Karmach

The 1-atm line gives the normal points

The 1-atm line crosses the fusion curve at the normal melting point and the vaporization curve at the normal boiling point. For water: 0 °C and 100 °C.

a horizontal path = constant pressure · a vertical path = constant temperature
follow the path and list every curve you cross: each crossing is one phase change
Dr. Karmach

The solid–liquid slope: water breaks the rule

Squeezing favors the denser phase, usually the solid, so fusion curves slope up-and-right. Water's leans up-and-left: ice is less dense than the liquid, so pressure pushes ice toward water.

CO₂: triple point at 5.1 atm, above 1 atm
the 1-atm line never reaches the fusion curve · dry ice sublimes instead of melting
Dr. Karmach

Reading a phase diagram

  1. Find the point. T across, P up; its region names the phase.
  2. Choose the path. Constant P: horizontal. Constant T: vertical.
  3. Cross the curves. Each crossing is one phase change.
  4. Check the specials. Triple point, critical point.
Dr. Karmach

The route through a phase diagram

A state question stops after step 1. A path question lists every curve it crosses, in order, then checks that list against the triple point and the critical point.

Dr. Karmach

Guided example: water at 25 °C

water at 25 °C: once at 80 kPa, once at 1 kPa
given: water's phase diagram in kPa · wanted: the state at each point

Find the state of water at each point. Three moves per point: temperature across, pressure up, read the region.

Dr. Karmach

Guided example: solution

Step 1 · Find the point

Move 1: across the bottom to 25 °C. Move 2: up to 80 kPa. Move 3: the spot lies between the fusion and vaporization curves, so the water is liquid.

Dr. Karmach

Guided example: solution


Step 1 · Find the point
Same 25 °C, now down to 1 kPa. The point drops below the vaporization curve: gas.

25 °C, 80 kPa → liquid · 25 °C, 1 kPa → gas
one temperature, two pressures · the vaporization curve lies between them
Dr. Karmach

Guided example: solution


Step 1 · Find the point

25 °C, 80 kPa → liquid · 25 °C, 1 kPa → gas
one temperature, two pressures · the vaporization curve lies between them
Water's vapor pressure at 25 °C is 3.17 kPa. At 80 kPa the outside pressure is higher: liquid. At 1 kPa it is lower: gas. ✓
Dr. Karmach

Guided example: the route on the map

25 °C, 80 kPa → liquid · 25 °C, 1 kPa → gas
given: two points on water's diagram · found: the state at each

A state question: step 1 only. With no path, no curve is crossed. ✓
Dr. Karmach

Worked example 1: heat a solid at constant pressure

start: solid, at a pressure just above the triple-point pressure
given: a pure substance with a normal (positive-slope) fusion curve · path: heat at constant pressure · wanted: the phases crossed

The sample starts cold, in the solid region. Heat it at constant pressure until it is well past its boiling point. List the phases it passes through.

Dr. Karmach

Worked example 1: solution

start: solid, just above the triple-point pressure
heat at constant pressure · normal fusion curve

Step 1 · Find the point

The start sits in the solid region, so the sample begins solid.

Dr. Karmach

Worked example 1: solution

start: solid, just above the triple-point pressure
heat at constant pressure · normal fusion curve
Step 1 · Find the point Step 2 · Choose the path

Heating at constant pressure is a horizontal path to the right.

Dr. Karmach

Worked example 1: solution

start: solid, just above the triple-point pressure
heat at constant pressure · normal fusion curve
Step 1 · Find the point Step 2 · Choose the path Step 3 · Cross the curves

Above the triple point, the path crosses the fusion curve first, then the vaporization curve.

solid → (cross fusion) → liquid → (cross vaporization) → gas
two curves crossed = two phase changes: melts, then boils
Dr. Karmach

Worked example 1: solution

start: solid, just above the triple-point pressure
heat at constant pressure · normal fusion curve
Step 1 · Find the point Step 2 · Choose the path Step 3 · Cross the curves
solid → (cross fusion) → liquid → (cross vaporization) → gas
two curves crossed = two phase changes: melts, then boils
Below the triple-point pressure, the same rightward path would cross only the sublimation curve: solid straight to gas, no liquid. ✓
Dr. Karmach

Worked example 1: the route on the map

solid → (cross fusion) → liquid → (cross vaporization) → gas
heat at constant pressure · the path runs above the triple-point pressure

Above the triple point, both the fusion and the vaporization curves lie in the path. ✓
Dr. Karmach

Worked example 2: reading substance X

substance X at 30 °C and 1 atm, heated at constant pressure to 100 °C
wanted: the starting phase, and each phase change with its temperature

Read the diagram. Name the starting phase, then each phase change and its temperature.

Dr. Karmach

Worked example 2: solution

Step 1 · Find the point

On the 1-atm line, 30 °C lies between the fusion crossing (−15 °C) and the vaporization crossing (60 °C). That is the liquid region.

Dr. Karmach

Worked example 2: solution


Step 1 · Find the point
Step 2 · Choose the path

Constant pressure: move right along the 1-atm line, from 30 °C to 100 °C.

Dr. Karmach

Worked example 2: solution


Step 1 · Find the point
Step 2 · Choose the path
Step 3 · Cross the curves

liquid (30 °C) → vaporization curve at 60 °C → gas (100 °C)
one curve crossed = one phase change · X boils at 60 °C, its normal boiling point
The triple point (0.40 atm) lies below this path; the critical point (150 °C) lies past its end. ✓
Dr. Karmach

Worked example 2: the route on the map

liquid (30 °C) → vaporization curve at 60 °C → gas (100 °C)
substance X · 1 atm, above the 0.40-atm triple point · ends below the 150 °C critical temperature

The path started past the fusion curve, so only one crossing remained. ✓
Dr. Karmach

Your turn: squeeze water vapor at −5 °C

starts as: · first curve: → becomes · second curve: → becomes

Follow the vertical path up from low pressure. Watch which way water's fusion curve leans.

Dr. Karmach

Your turn: squeeze water vapor at −5 °C

starts as: · first curve: → becomes · second curve: → becomes
gas → (sublimation curve) → solid → (fusion curve) → liquid
two crossings · the left-leaning fusion curve means enough pressure melts ice below 0 °C
Dr. Karmach

Your turn: the route on the map

gas → (sublimation curve) → solid → (fusion curve) → liquid
water · constant −5 °C · squeezed up from low pressure

A vertical path holds the temperature. At −5 °C it starts left of the triple point, so the sublimation curve comes first. ✓
Dr. Karmach

Where this goes wrong

Swapping the axes. Temperature is the horizontal axis, pressure the vertical: read T across the bottom, P up the side, not the reverse.
Confusing the two special points. The triple point is where all three phases coexist; the critical point is where the liquid–gas distinction ends. They are different spots.
Assuming everything melts at 1 atm. If the triple point is above 1 atm (CO₂, 5.1 atm), the 1-atm line never reaches the fusion curve: the solid sublimes instead of melting.
Treating water's fusion line as normal. Water's solid–liquid line slopes up-to-the-left; ice is less dense than water, so raising the pressure on ice can melt it.
Dr. Karmach

Practice 1

What is the state of water at −10 °C and 50 kPa?

  1. liquid
  2. solid
  3. gas
Dr. Karmach

Practice 1 answer: B

−10 °C across, 50 kPa up → left of the fusion curve, above the sublimation curve
the solid region · answer B

A took the left-leaning fusion curve to mean cold water under pressure is liquid; at −10 °C that needs about 110,000 kPa (1,100 atm), and 50 kPa is half an atmosphere. C read any pressure below 101.3 kPa as gas; at −10 °C the gas region lies below 0.26 kPa.

Below 0 °C, and far above the 0.61-kPa triple point: ice. ✓
Dr. Karmach

Practice 1: the route on the map

−10 °C, 50 kPa → solid
given: one point on water's diagram · found: its state

The same single step as the guided example: find the point, read the region. ✓
Dr. Karmach

Practice 2

Substance Y is warmed at 1 atm from 0 °C to 200 °C. What happens?

  1. Sublimes at 10 °C, straight from solid to gas
  2. Melts at 10 °C, then boils at 118 °C
  3. Melts at 14 °C, then boils at 118 °C
  4. Melts at 14 °C and is still liquid at 200 °C
Dr. Karmach

Practice 2 answer: C

1-atm line: fusion curve at 14 °C · vaporization curve at 118 °C → melts at 14 °C, boils at 118 °C, answer C

A put the triple point on the path, but it sits at 0.25 atm, 0.75 atm below it. B read the triple-point temperature, 10 °C, as the melting point: 4 °C too low. D took the critical point, 320 °C, as the boiling point: 202 °C too high.

1 atm is above Y's triple-point pressure, so Y melts and then boils, like any normal substance in open air. ✓
Dr. Karmach

Practice 2: the route on the map

1-atm line: melts at 14 °C, then boils at 118 °C
substance Y · heated at 1 atm, above the 0.25-atm triple point

The same two crossings as worked example 1, now with temperatures read off the axis. ✓
Dr. Karmach

Practice 3: freeze-drying

water: triple point 0.01 °C, 0.61 kPa · normal melting point 0 °C · normal boiling point 100 °C
frozen strawberries at −30 °C · held at 0.10 kPa · warmed at constant pressure to 20 °C

A freeze-dryer pumps the pressure down, then warms the frozen fruit. What happens to the ice?

  1. It sublimes: solid straight to gas
  2. It melts at 0 °C and is still liquid at 20 °C
  3. It melts, then the water boils away
  4. It undergoes deposition
Dr. Karmach

Practice 3 answer: A

0.10 kPa lies below the 0.61-kPa triple point → the path meets only the sublimation curve · answer A
0.61 − 0.10 = 0.51 kPa below the triple point · the ice turns to vapor near −20 °C

B used the 1-atm points: 0 °C and 100 °C hold only at 101.3 kPa. C sent the path through the liquid region, which exists only above 0.61 kPa. D named the change backward: deposition runs gas → solid.

No liquid ever forms, so the fruit dries without turning soggy. That is the point of freeze-drying. ✓
Dr. Karmach

Practice 3: the route on the map

ice at 0.10 kPa → (sublimation curve) → vapor
water · heated at constant pressure · 0.10 kPa < 0.61 kPa

Below the triple-point pressure, a heating path meets one curve only. ✓
Dr. Karmach

Practice 4

substance W: triple point 3.2 atm, −28 °C · critical point 48 atm, 96 °C
normal fusion curve · a gas at 20 atm and 120 °C is cooled at constant pressure to −60 °C

Which phase changes occur along the way?

  1. Deposition only (gas → solid)
  2. Condensation (gas → liquid), then freezing (liquid → solid)
  3. None: it starts above the critical temperature, so it never condenses
  4. Condensation only (gas → liquid)
Dr. Karmach

Practice 4 answer: B

20 atm: above the 3.2-atm triple point · below the 48-atm critical point → condenses, then freezes, answer B

The horizontal path runs 16.8 atm above the triple point, so cooling crosses the vaporization curve, then the fusion curve. It ends at −60 °C, 32 °C below the triple-point temperature: solid.

A took the sublimation route, which runs only below 3.2 atm. D stopped at the liquid; the path continues past the fusion curve. C misread the critical point: the gas starts 24 °C above the critical temperature, but cooling carries it below 96 °C, and at 20 atm, 28 atm under the critical pressure, it condenses.

Compare the path's pressure with both special points first. Between them, a cooling gas condenses and then freezes. ✓
Dr. Karmach

Practice 4: the route on the map

20 atm: condenses, then freezes
substance W · 3.2 atm < 20 atm < 48 atm · cooled from 120 °C to −60 °C

Cooling runs the path right to left, so each curve is crossed in reverse: condense, then freeze. ✓
Dr. Karmach

Practice 5

substance Q: triple point −35 °C, 0.80 atm · critical point 120 °C, 38 atm
fusion curve slopes up to the right · start: gas at 60 °C, 0.20 atm · squeezed at 60 °C up to 50 atm

What does the sample go through as the pressure rises?

  1. Deposition only (gas → solid)
  2. Condensation (gas → liquid), then freezing (liquid → solid)
  3. No change: past 38 atm it is a supercritical fluid
  4. Condensation only (gas → liquid)
Dr. Karmach

Practice 5 answer: D

60 °C − (−35 °C) = 95 °C above the triple point · 120 °C − 60 °C = 60 °C below the critical point → condensation only, answer D

The vertical path at 60 °C crosses the vaporization curve once. The steep fusion curve rises from −35 °C and never reaches 60 °C.

A compared the starting 0.20 atm with the 0.80-atm triple point; a vertical path is judged by its temperature. B went on across the fusion curve, as a cooling path would. C checked only the pressure: 50 atm is 12 atm past 38 atm, but a supercritical fluid also needs a temperature above 120 °C.

Between the triple-point and critical temperatures, squeezing a gas makes a liquid, and more pressure keeps it liquid. ✓
Dr. Karmach

Practice 5: the route on the map

0.20 atm → 50 atm at 60 °C: condenses
substance Q · −35 °C < 60 °C < 120 °C

A vertical path is checked by its temperature. Between the triple point and the critical point, it crosses one curve. ✓
Dr. Karmach

Check yourself

  1. A substance with a normal fusion curve is heated at a constant pressure above its triple point. Which curve does the path cross first, and what phase change is it?
  2. Why can raising the pressure on ice just below 0 °C melt it, when raising the pressure on most solids does the opposite?

The solid region of any phase diagram hides very different kinds of solid. Sorting them by the particles they are built from explains why some melt near room temperature and others far above 1000 °C.

Dr. Karmach

5 · Heat of a Phase Change

Find the heat of a phase change with q = mass × ΔH in J/g or q = n × ΔH in kJ/mol, choosing the heat of fusion for melting or freezing and the heat of vaporization for boiling or condensing, while the temperature holds constant.

Dr. Karmach

Heat flows, the temperature holds

A glass of ice water stays at 0 °C until the last cube melts. Sweat cools your skin. Heat moves in or out; the temperature holds.

Dr. Karmach

Temperature holds during a phase change

A phase change runs at one temperature. The heat does not warm the sample; it pulls the molecules apart. Ice water holds at 0 °C until the last cube melts.

Dr. Karmach

A fixed heat for every mole

melting ice at 0 °C takes 6.02 kJ per mole
twice the moles, twice the heat · the temperature stays at 0 °C the whole time

Each mole of ice takes the same heat to melt. As a conversion factor, that heat cancels moles:

2.00 mol × 6.02 kJ1 mol = 12.0 kJ

How much heat melts 0.500 mol of ice?

Dr. Karmach

A fixed heat for every mole

melting ice at 0 °C takes 6.02 kJ per mole
twice the moles, twice the heat · the temperature stays at 0 °C the whole time

Each mole of ice takes the same heat to melt. As a conversion factor, that heat cancels moles:

2.00 mol × 6.02 kJ1 mol = 12.0 kJ

How much heat melts 0.500 mol of ice?

0.500 mol × 6.02 kJ1 mol = 3.01 kJ

Half a mole takes half the heat.

Dr. Karmach

Six changes of state

Changes toward the gas pull particles apart and absorb heat: endothermic. The reverses release that same heat: exothermic. Vaporization is also called evaporation. Dry ice goes straight from solid to gas; so does iodine warmed gently.

Dr. Karmach

Heat of fusion and heat of vaporization

for water: ΔHfus = 335 J/g · ΔHvap = 2259 J/g
melt or freeze: 335 J per gram · boil or condense: 2259 J per gram

Melting is called fusion. The heat of fusion, ΔHfus, melts one gram; the heat of vaporization, ΔHvap, boils one gram. Freezing and condensing release the same amounts, reversed.

Dr. Karmach

Vaporizing costs more than melting

ΔHvap is far larger than ΔHfus. Melting only loosens the packing; the molecules still touch. Vaporizing pulls them fully apart, which takes about seven times the energy.

Dr. Karmach

The phase-change heat equation

q = mass × ΔH
g × (J/g) = J · absorbed (+) to melt or boil · released (−) to freeze or condense

Each heat is a conversion factor in joules per gram. Multiply by the mass and grams cancel. Melting and boiling absorb heat; freezing and condensing release it, so q turns negative.

Dr. Karmach

The same heats, per mole

q = n × ΔH
for water: ΔHfus = 6.02 kJ/mol · ΔHvap = 40.7 kJ/mol · grams → moles → kilojoules

Phase-change heats also come per mole: 6.02 kJ melts a mole of ice, 40.7 kJ boils a mole of water. A mass in grams becomes moles first; either route lands on the same heat.

Dr. Karmach

The method

  1. Name the phase change.
  2. Pick its ΔH: fusion to melt or freeze, vaporization to boil or condense.
  3. Multiply: mass × ΔH (J/g), or moles × ΔH (kJ/mol).
  4. Set the direction: melting and boiling absorb; freezing and condensing release.

Dr. Karmach

Guided example: boiling off a pot of water

q = n × ΔH
given: 2.50 mol water boils at 100 °C · ΔHfus = 6.02 kJ/mol · ΔHvap = 40.7 kJ/mol · wanted: q in kJ

A pot of water at 100 °C boils until 2.50 mol of it has turned to steam. How much heat did the water absorb, in kJ?

Two molar heats are listed. Name the change first; the change picks the heat.

Dr. Karmach

Guided example: solution

q = n × ΔH
given: 2.50 mol water boils at 100 °C · ΔHfus = 6.02 kJ/mol · ΔHvap = 40.7 kJ/mol

Step 1 · Name the phase change

Liquid water turns to steam at 100 °C. The change is boiling.

Dr. Karmach

Guided example: solution

q = n × ΔH
given: 2.50 mol water boils at 100 °C · ΔHfus = 6.02 kJ/mol · ΔHvap = 40.7 kJ/mol
Step 1 · Name the phase change Step 2 · Pick its ΔH

Boiling uses the heat of vaporization, 40.7 kJ/mol. The 6.02 kJ/mol melts ice; it has no part here.

Dr. Karmach

Guided example: solution

q = n × ΔH
given: 2.50 mol water boils at 100 °C · ΔHfus = 6.02 kJ/mol · ΔHvap = 40.7 kJ/mol
Step 1 · Name the phase change Step 2 · Pick its ΔH Step 3 · Multiply
2.50 mol × 40.7 kJ1 mol = 102 kJ

Moles cancel; kilojoules remain.

Dr. Karmach

Guided example: solution

q = n × ΔH
given: 2.50 mol water boils at 100 °C · ΔHfus = 6.02 kJ/mol · ΔHvap = 40.7 kJ/mol
Step 1 · Name the phase change Step 2 · Pick its ΔH Step 3 · Multiply
2.50 mol × 40.7 kJ1 mol = 102 kJ
Step 4 · Set the direction
Boiling absorbs heat, so q is positive: q = +102 kJ. Each mole takes about 41 kJ, so 2.50 mol take about 100 kJ. ✓
Dr. Karmach

Guided example: the route on the map

q = n × ΔHvap
given: 2.50 mol water boils at 100 °C · found: q = +102 kJ

Boiling picks ΔHvap and a plus sign. Moles were given, so the route starts at the moles box: one factor to kilojoules. ✓
Dr. Karmach

Practice 1

q = n × ΔH
given: 1.60 mol steam condenses at 100 °C · ΔHfus = 6.02 kJ/mol · ΔHvap = 40.7 kJ/mol

Shower steam at 100 °C hits a cold mirror, and 1.60 mol of it condenses to liquid water. How much heat, in kJ, does the steam release?

  1. 9.63
  2. 0.0393
  3. 40.7
  4. 65.1
Dr. Karmach

Practice 1 answer: D

q = n × ΔHvap
condensing is boiling reversed: the vaporization heat applies · 1.60 mol · wanted: heat released
1.60 mol × 40.7 kJ1 mol = 65.1 kJ · answer D

A used the heat of fusion: 1.60 × 6.02 = 9.63, but nothing melts or freezes. B put the heat per mole upside down: 1.60 ÷ 40.7 = 0.0393, and moles do not cancel. C is the heat for one mole alone; the steam is 1.60 mol.

Condensing releases what boiling absorbs, 40.7 kJ per mole, so q for the steam is −65.1 kJ. ✓
Dr. Karmach

Practice 1: the route on the map

q = n × ΔHvap
given: 1.60 mol steam condenses at 100 °C · found: 65.1 kJ released

Condensing sits in the releases column with ΔHvap. Moles were given: one factor to kilojoules. ✓
Dr. Karmach

Worked example 1: melt ice

q = mass × ΔHfus
given: 60.0 g ice at 0 °C · ΔHfus = 335 J/g · wanted: q

A tray holds 60.0 g of ice at 0 °C. How much heat melts it completely? (ΔHfus of water: 335 J/g)

Name the change of state, then pick its heat.

Dr. Karmach

Worked example 1: solution

q = mass × ΔHfus
given: 60.0 g ice at 0 °C · ΔHfus = 335 J/g · wanted: q

Step 1 · Name the phase change

The ice is melting: solid water turns to liquid, all at 0 °C.

Dr. Karmach

Worked example 1: solution

q = mass × ΔHfus
given: 60.0 g ice at 0 °C · ΔHfus = 335 J/g · wanted: q
Step 1 · Name the phase change Step 2 · Pick its ΔH

Melting uses the heat of fusion, ΔHfus = 335 J/g.

Dr. Karmach

Worked example 1: solution

q = mass × ΔHfus
given: 60.0 g ice at 0 °C · ΔHfus = 335 J/g · wanted: q
Step 1 · Name the phase change Step 2 · Pick its ΔH Step 3 · Multiply

Write the factor so grams cancel. Only one orientation does:

335 J1 g cancels grams ✓    1 g335 J cancels nothing ✗
60.0 g × 335 J1 g = 20,100 J
Dr. Karmach

Worked example 1: solution

q = mass × ΔHfus
given: 60.0 g ice at 0 °C · ΔHfus = 335 J/g · wanted: q
Step 1 · Name the phase change Step 2 · Pick its ΔH Step 3 · Multiply
60.0 g × 335 J1 g = 20,100 J
Step 4 · Set the direction
Melting absorbs heat, so q is positive: 20,100 J (20.1 kJ) go in, and the temperature never leaves 0 °C. ✓
Dr. Karmach

Worked example 1: the route on the map

q = mass × ΔHfus
given: 60.0 g ice at 0 °C · found: q = +20,100 J

Melting picks ΔHfus and a plus sign. Grams in with a per-gram heat: the top lane, one factor. ✓
Dr. Karmach

Worked example 2: boil water to steam

q = mass × ΔHvap
given: 20.0 g water at 100 °C · ΔHvap = 2259 J/g · wanted: q

20.0 g of water at 100 °C boils away to steam. How much heat does it take? (ΔHvap of water: 2259 J/g)

Same route as melting, with the vaporization heat.

Dr. Karmach

Worked example 2: solution

q = mass × ΔHvap
given: 20.0 g water at 100 °C · ΔHvap = 2259 J/g · wanted: q

Step 1 · Name the phase change

The water is boiling: liquid turns to gas, all at 100 °C.

Dr. Karmach

Worked example 2: solution

q = mass × ΔHvap
given: 20.0 g water at 100 °C · ΔHvap = 2259 J/g · wanted: q
Step 1 · Name the phase change Step 2 · Pick its ΔH

Boiling uses the heat of vaporization, ΔHvap = 2259 J/g.

Dr. Karmach

Worked example 2: solution

q = mass × ΔHvap
given: 20.0 g water at 100 °C · ΔHvap = 2259 J/g · wanted: q
Step 1 · Name the phase change Step 2 · Pick its ΔH Step 3 · Multiply
20.0 g × 2259 J1 g = 45,180 J

Grams cancel; joules remain.

Dr. Karmach

Worked example 2: solution

q = mass × ΔHvap
given: 20.0 g water at 100 °C · ΔHvap = 2259 J/g · wanted: q
Step 1 · Name the phase change Step 2 · Pick its ΔH Step 3 · Multiply
20.0 g × 2259 J1 g = 45,180 J
Step 4 · Set the direction
Boiling absorbs heat: q = +45,180 J (45.2 kJ). Same 20.0 g would take only 6,700 J to melt: vaporizing costs far more. ✓
Dr. Karmach

Worked example 2: the route on the map

q = mass × ΔHvap
given: 20.0 g water at 100 °C · found: q = +45,180 J

Boiling picks ΔHvap. Same top lane as melting; only the factor changed. ✓
Dr. Karmach

Your turn: melt more ice

q = mass × ΔHfus
given: 40.0 g ice at 0 °C · ΔHfus = 335 J/g · wanted: q

40.0 g of ice at 0 °C melts to water. Fill in the heat of fusion, then compute.

40.0 g × J1 g = J
Dr. Karmach

Your turn: melt more ice

q = mass × ΔHfus
given: 40.0 g ice at 0 °C · ΔHfus = 335 J/g · wanted: q

40.0 g of ice at 0 °C melts to water. Fill in the heat of fusion, then compute.

40.0 g × J1 g = J
40.0 g × 335 J1 g = 13,400 J
335 J melts one gram, so 40.0 g take 40.0 × 335 = 13,400 J (13.4 kJ), all at 0 °C. ✓
Dr. Karmach

Where this goes wrong

q = mass × ΔHfus
60.0 g ice at 0 °C · ΔHfus = 335 J/g · correct q = 20,100 J
Leaving out the mass. 335 J melts a single gram. The sample has 60.0 of them. Scale it up: 60.0 g × 335 J/g = 20,100 J.
Dividing by the heat of fusion. 60.0 ÷ 335 = 0.179, in units of g²/J. Nothing cancels. Write the factor so grams cancel: 60.0 g × (335 J / 1 g).
Reporting kilojoules as joules. 60.0 × 335 = 20,100, then sliding the decimal gives 20.1. That is the value in kilojoules. In joules it is 20,100 J.
Using the vaporization heat to melt. Melting uses ΔHfus = 335 J/g, not ΔHvap = 2259 J/g. 60.0 × 2259 = 135,540 J is the heat to boil the water, not melt the ice.
Dr. Karmach

Practice 2

q = mass × ΔHvap
given: 5.00 × 10⁴ J absorbed by water at 100 °C · ΔHvap = 2259 J/g · wanted: mass boiled away

A kettle delivers 5.00 × 10⁴ J to water already boiling at 100 °C. What mass of water, in grams, boils away? (ΔHvap of water: 2259 J/g)

  1. 22.1
  2. 149
  3. 1.20 × 10⁴
  4. 1.13 × 10⁸
Dr. Karmach

Practice 2 answer: A

q = mass × ΔHvap
given: 5.00 × 10⁴ J absorbed at 100 °C · ΔHvap = 2259 J/g · wanted: g
5.00 × 10⁴ J × 1 g2259 J = 22.1 g · answer A

The heat is given, so ΔHvap enters upside down: J on the bottom, so joules cancel. B used the heat of fusion: 5.00 × 10⁴ ÷ 335 = 149 g is the ice this heat would melt, not the water it boils. C used water's specific heat: 5.00 × 10⁴ ÷ 4.184 = 1.20 × 10⁴, but a plateau has no ΔT, so c does not apply. D kept the factor right side up: 5.00 × 10⁴ × 2259 = 1.13 × 10⁸, in J²/g, nothing cancels.

Each gram takes 2259 J to boil, so 50,000 J boils a little over 20 g. ✓
Dr. Karmach

Practice 2: the route on the map

q = mass × ΔHvap
given: 5.00 × 10⁴ J absorbed at 100 °C · found: 22.1 g boiled away

The heat was given, so the top lane runs backward: ΔHvap upside down, joules cancel, grams remain. ✓
Dr. Karmach

Worked example 3: a steam burn

q = mass × ΔHvap
given: 8.00 g steam at 100 °C → water at 100 °C · ΔHvap = 2259 J/g · wanted: heat released

8.00 g of steam at 100 °C condenses on skin and releases heat. This is why a steam burn is so severe. How much heat comes out?

A common first attempt: add a q = mass × c × ΔT term for the temperature. Test it.

Dr. Karmach

Worked example 3: solution

q = mass × ΔHvap
8.00 g steam · condenses at 100 °C → water at 100 °C · wanted: heat released

A common first attempt

m·c·ΔT = 8.00 g × 4.184 J/g·°C × (100 − 100) °C = 0 J

The steam condenses at 100 °C into water at 100 °C. ΔT = 0, so the m·c·ΔT term adds nothing.

Dr. Karmach

Worked example 3: solution

q = mass × ΔHvap
8.00 g steam · condenses at 100 °C → water at 100 °C · wanted: heat released

A common first attempt

m·c·ΔT = 8.00 g × 4.184 J/g·°C × (100 − 100) °C = 0 J

The steam condenses at 100 °C into water at 100 °C. ΔT = 0, so the m·c·ΔT term adds nothing.
Step 1 · Name the phase change

The steam is condensing: gas turns to liquid, all at 100 °C.

Dr. Karmach

Worked example 3: solution

q = mass × ΔHvap
8.00 g steam · condenses at 100 °C → water at 100 °C · wanted: heat released

A common first attempt

m·c·ΔT = 8.00 g × 4.184 J/g·°C × (100 − 100) °C = 0 J

The steam condenses at 100 °C into water at 100 °C. ΔT = 0, so the m·c·ΔT term adds nothing.
Step 1 · Name the phase change
Step 2 · Pick its ΔH

Condensing uses the heat of vaporization, ΔHvap = 2259 J/g, the same value as boiling.

No temperature change means no m·c·ΔT term. The phase-change heat is the whole answer. ✓
Dr. Karmach

Worked example 3: heat released

q = mass × ΔHvap
8.00 g steam condensing at 100 °C · ΔHvap = 2259 J/g

Step 3 · Multiply

8.00 g × 2259 J1 g = 18,072 J
Dr. Karmach

Worked example 3: heat released

q = mass × ΔHvap
8.00 g steam condensing at 100 °C · ΔHvap = 2259 J/g
Step 3 · Multiply
8.00 g × 2259 J1 g = 18,072 J
Step 4 · Set the direction

Heat leaves the steam as it condenses, so q is negative: q = −18,072 J.

Condensing just 8.00 g of steam dumps 18,072 J (18.1 kJ) into the skin, all at 100 °C before the water even starts to cool. That is why steam burns are severe. ✓
Dr. Karmach

Worked example 3: the route on the map

q = mass × ΔHvap
given: 8.00 g steam condenses at 100 °C · found: q = −18,072 J

Condensing sits in the releases column: ΔHvap with a minus sign. The route is the top lane, with no m·c·ΔT anywhere. ✓
Dr. Karmach

Practice 3

q = mass × ΔH
given: 45.0 g water at 0 °C freezes · ΔHfus = 335 J/g · ΔHvap = 2259 J/g

An ice-cube tray holds 45.0 g of water at 0 °C, and all of it freezes. What is q for the water, sign included, in joules?

  1. 1.51 × 10⁴
  2. −1.02 × 10⁵
  3. −1.51 × 10⁴
  4. −0.134
Dr. Karmach

Practice 3 answer: C

q = mass × ΔHfus
freezing is melting reversed: the fusion heat applies, and heat leaves the water
45.0 g × 335 J1 g = 15,075 J → q = −1.51 × 10⁴ J · answer C

A dropped the sign: freezing releases heat, so q for the water is negative. B used the heat of vaporization: −(45.0 × 2259) = −1.02 × 10⁵, but nothing boils or condenses. D divided by the heat of fusion: 45.0 ÷ 335 = 0.134, and grams do not cancel.

Melting the same 45.0 g would absorb +1.51 × 10⁴ J. Freezing hands that heat back, so q = −1.51 × 10⁴ J. ✓
Dr. Karmach

Practice 3: the route on the map

q = mass × ΔHfus
given: 45.0 g water at 0 °C freezes · found: q = −1.51 × 10⁴ J

Freezing picks ΔHfus and a minus sign. Grams in with a per-gram heat: the top lane, one factor. ✓
Dr. Karmach

Worked example 4: melting by the molar route

q = n × ΔHfus
given: 60.0 g ice at 0 °C · ΔHfus = 6.02 kJ/mol · molar mass of water 18.02 g/mol · wanted: q in kJ

60.0 g of ice at 0 °C melts to water. Find the heat with the molar heat of fusion, 6.02 kJ/mol. The heat is per mole, so the grams must become moles first.

Dr. Karmach

Worked example 4: solution

q = n × ΔHfus
given: 60.0 g ice at 0 °C · ΔHfus = 6.02 kJ/mol · molar mass of water 18.02 g/mol

Step 1 · Name the phase change

The ice is melting at 0 °C, the same change as ever. Only the units of its heat are new: kilojoules per mole.

Dr. Karmach

Worked example 4: solution

q = n × ΔHfus
given: 60.0 g ice at 0 °C · ΔHfus = 6.02 kJ/mol · molar mass of water 18.02 g/mol
Step 1 · Name the phase change Step 2 · Pick its ΔH

Melting uses the heat of fusion: ΔHfus = 6.02 kJ/mol.

Dr. Karmach

Worked example 4: solution

q = n × ΔHfus
given: 60.0 g ice at 0 °C · ΔHfus = 6.02 kJ/mol · molar mass of water 18.02 g/mol
Step 1 · Name the phase change Step 2 · Pick its ΔH Step 3 · Multiply
60.0 g × 1 mol18.02 g × 6.02 kJ1 mol = 20.0 kJ

Grams cancel into moles, moles cancel into kilojoules.

Dr. Karmach

Worked example 4: solution

q = n × ΔHfus
given: 60.0 g ice at 0 °C · ΔHfus = 6.02 kJ/mol · molar mass of water 18.02 g/mol
Step 1 · Name the phase change Step 2 · Pick its ΔH Step 3 · Multiply
60.0 g × 1 mol18.02 g × 6.02 kJ1 mol = 20.0 kJ
Step 4 · Set the direction

The per-gram route on the same sample: 60.0 g × 335 J/g = 20,100 J = 20.1 kJ. Two routes, one heat, agreeing to the rounding of the constants.

Melting absorbs heat: q = +20.0 kJ. 3.33 mol of ice at 6.02 kJ each is about 20 kJ, and the 335 J/g route lands on the same number. ✓
Dr. Karmach

Worked example 4: the route on the map

q = n × ΔHfus
given: 60.0 g ice at 0 °C · found: q = +20.0 kJ

Grams given with a heat per mole: the bottom lane, molar mass first, then ΔHfus. Two factors. ✓
Dr. Karmach

Take-home: a phase change has no ΔT

temperature changes, one phase: q = m · c · ΔT
warming or cooling within a solid, liquid, or gas
temperature constant, changing phase: q = mass × ΔH or q = n × ΔH
melting, freezing, boiling, condensing. ΔT = 0, so no m·c·ΔT term

During a phase change the temperature holds, so ΔT = 0 and the m·c·ΔT term is zero. Use ΔH alone. The two never combine within one phase change.

Dr. Karmach

Practice 4

q = n × ΔH
given: 90.0 g water boiled away at 100 °C · ΔHfus = 6.02 kJ/mol · ΔHvap = 40.7 kJ/mol · water 18.02 g/mol

A pasta pot at a rolling boil loses 90.0 g of water to steam. How much heat, in kJ, did that water absorb?

  1. 30.1
  2. 3.66 × 10³
  3. 0.123
  4. 4.99
  5. 203
Dr. Karmach

Practice 4 answer: E

q = n × ΔHvap
boiling: the vaporization heat applies · 90.0 g water · 18.02 g/mol · 40.7 kJ/mol

Two conversion factors are needed.

90.0 g × 1 mol18.02 g × 40.7 kJ1 mol = 203 kJ · answer E

A used the heat of fusion: 4.99 × 6.02 = 30.1. B skipped the molar mass: 90.0 × 40.7 = 3.66 × 10³, as if each gram were a mole. C put the molar heat upside down: 4.99 ÷ 40.7 = 0.123. D stopped at moles: 4.99 mol, one factor short.

Boiling absorbs heat: q = +203 kJ. About 5 mol at about 41 kJ each is about 200 kJ. ✓
Dr. Karmach

Practice 4: the route on the map

q = n × ΔHvap
given: 90.0 g water boiled away at 100 °C · found: q = +203 kJ

Grams given with a heat per mole: the bottom lane, molar mass first, then ΔHvap. Two factors. ✓
Dr. Karmach

Practice 5

q = n × ΔH
given: 15.0 kJ removed from liquid water at 0 °C · ΔHfus = 6.02 kJ/mol · ΔHvap = 40.7 kJ/mol · water 18.02 g/mol · wanted: g of ice

A freezer removes 15.0 kJ of heat from liquid water at 0 °C. What mass of ice, in grams, forms?

  1. 6.64
  2. 44.9
  3. 0.138
  4. 2.49
Dr. Karmach

Practice 5 answer: B

q = n × ΔHfus
freezing is melting reversed: the fusion heat applies · 15.0 kJ released by the water · 18.02 g/mol
15.0 kJ × 1 mol6.02 kJ × 18.02 g1 mol = 44.9 g · answer B

The heat is given, so ΔHfus enters upside down and kJ cancels. A picked the vaporization heat: 15.0 ÷ 40.7 × 18.02 = 6.64 g, but no boiling or condensing happens here. C divided by the molar mass: 2.49 ÷ 18.02 = 0.138 g. D stopped at moles: 2.49 mol of water, one factor short of grams.

Freezing releases heat, so q for the water is −15.0 kJ; the mass of ice is positive. 2.49 mol at 18.02 g each is about 45 g. ✓
Dr. Karmach

Practice 5: the route on the map

q = n × ΔHfus
given: 15.0 kJ removed from water at 0 °C · found: 44.9 g of ice

Freezing picks ΔHfus. The heat was given, so the bottom lane runs backward: kilojoules to moles, then moles to grams. ✓
Dr. Karmach

Check yourself

  1. A block of ice at 0 °C melts to water at 0 °C. What happens to the temperature while it melts, and where does the heat go?
  2. Which is larger for water, the heat of fusion or the heat of vaporization, and why?

Melting and boiling are the flat steps of a heating curve. Between those steps the temperature climbs, and there q = m·c·ΔT takes over. The full curve chains both kinds of heat, segment by segment.

Dr. Karmach

6 · Heating & Cooling Curves

Break a heating path into segments, use q = m·c·ΔT for each slope and the phase-change energy for each plateau, and add them for the total heat.

Dr. Karmach

From the freezer to a rolling boil

Heat a block of ice steadily. Temperature climbs, holds at 0 °C while it melts, climbs, then holds at 100 °C while it boils.

Dr. Karmach

Reading a heating curve, one segment at a time

Heat flows in steadily. The temperature climbs while one phase warms and holds while the phase changes. Which letter shows ice and liquid water together? Which shows liquid water warming?

Dr. Karmach

Reading a heating curve, one segment at a time

Heat flows in steadily. The temperature climbs while one phase warms and holds while the phase changes. Which letter shows ice and liquid water together? Which shows liquid water warming?

B: ice and liquid water together, melting at 0 °C · C: liquid water warming from 0 to 100 °C
read right to left, the same path is a cooling curve: steam condenses along D, water freezes along B
Dr. Karmach

Warming and phase changes alternate

Heating a substance alternates between warming one phase (a sloped step, q = m·c·ΔT) and changing the phase (a flat step, phase-change energy). The total heat is the sum of every step.

Dr. Karmach

Two kinds of segment, two equations

sloped segment: one phase warming
q = m · c · ΔT · uses that phase's specific heat c
flat plateau: a phase change at constant T
q = m · ΔH · the temperature does not move, so there is no ΔT

Read the graph one segment at a time. A slope warms a single phase. A plateau holds the temperature fixed while the phase changes. Each segment needs its own equation.

Dr. Karmach

Water's constants for each segment

slopes: q = m · c · ΔT
c(ice) = 2.03 · c(liquid water) = 4.184 · c(steam) = 1.9 J/g·°C
plateaus: q = m · ΔH
ΔHfus = 335 J/g at 0 °C · ΔHvap = 2259 J/g at 100 °C

Each phase carries its own specific heat. Each phase change carries its own energy. Ice and steam sit near 2 J/g·°C; only liquid water earns 4.184.

Dr. Karmach

The method

  1. Identify each segment. Each slope and each plateau is one piece.
  2. Compute each piece. A slope uses q = m·c·ΔT with that phase's c. A plateau uses the phase-change energy, ΔHfus or ΔHvap.
  3. Add every piece for the total.
Dr. Karmach

Guided example: water to steam

total q = warm water + boil
given: 40.0 g water at 80.0 °C → steam at 100 °C · c(water) = 4.184 J/g·°C · ΔHvap = 2259 J/g · wanted: q

A kettle holds 40.0 g of water at 80.0 °C. It heats until all of the water has boiled away as steam at 100 °C. How much heat does that take?

Find the start and the end on the curve, then follow it between them.

Dr. Karmach

Guided example: solution

total q = warm water + boil
given: 40.0 g water at 80.0 °C → steam at 100 °C · c(water) = 4.184 J/g·°C · ΔHvap = 2259 J/g

Step 1 · Identify each segment

Two pieces. The liquid warms from 80.0 °C to 100 °C, a slope. Then it boils at 100 °C, a plateau.

Dr. Karmach

Guided example: solution

total q = warm water + boil
given: 40.0 g water at 80.0 °C → steam at 100 °C · c(water) = 4.184 J/g·°C · ΔHvap = 2259 J/g
Step 1 · Identify each segment Step 2 · Compute each piece
warm water: 40.0 g × 4.184 J1 g·°C × 20.0 °C = 3347 J · boil: 40.0 g × 2259 J1 g = 90,360 J

The slope has a ΔT of 20.0 °C. The plateau has none, so ΔHvap alone gives its heat.

Dr. Karmach

Guided example: solution

total q = warm water + boil
given: 40.0 g water at 80.0 °C → steam at 100 °C · c(water) = 4.184 J/g·°C · ΔHvap = 2259 J/g
Step 1 · Identify each segment Step 2 · Compute each piece
warm water: 40.0 g × 4.184 J1 g·°C × 20.0 °C = 3347 J · boil: 40.0 g × 2259 J1 g = 90,360 J
Step 3 · Add every piece
q = 3347 J + 90,360 J = 93,707 J = 9.37 × 10⁴ J
Boiling costs 27 times the warming. Almost all the heat goes into the plateau. ✓
Dr. Karmach

Guided example: the route on the curve

total q = warm water + boil
given: 40.0 g water, 80.0 °C → steam, 100 °C · found: q = 9.37 × 10⁴ J

Two pieces lie between the start and the end: one slope, one plateau. ✓
Dr. Karmach

Practice 1

total q = the sum of every segment crossed
given: ice at −15 °C → liquid water at 60 °C · wanted: the pieces

A snowball at −15 °C goes into a hot pot and ends as liquid water at 60 °C. Which pieces make up the total heat?

  1. warm ice + melt + warm water
  2. melt + warm water
  3. warm ice + warm water
  4. warm ice + melt
Dr. Karmach

Practice 1 answer: A

ice at −15 °C → liquid water at 60 °C
warm ice, −15 → 0 °C · melt at 0 °C · warm water, 0 → 60 °C · 60 °C is below 100 °C, so nothing boils

B started at the melting point: the ice must first warm from −15 °C to 0 °C. C skipped the plateau: melting takes heat even though the temperature holds. D stopped at the melting point: the water still has to warm to 60 °C.

Three pieces, answer A: two slopes and the plateau between them. ✓
Dr. Karmach

Practice 1: the route on the curve

ice at −15 °C → liquid water at 60 °C
three pieces: warm ice · melt · warm water

Each segment between the start and the end is one piece. Boiling lies past the end. ✓
Dr. Karmach

Worked example 1: ice at 0 °C to warm water

total q = melt + warm
given: 30 g ice at 0 °C → liquid water at 25 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C · wanted: q

A 30 g block of ice, already at 0 °C, is heated until it becomes liquid water at 25 °C. How much heat does it take?

Identify each segment, then add the pieces.

Dr. Karmach

Worked example 1: solution

total q = melt + warm
given: 30 g ice at 0 °C → liquid water at 25 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C

Step 1 · Identify each segment

The ice sits at its melting point. Two pieces follow: melt at a constant 0 °C, then warm the liquid to 25 °C.

Dr. Karmach

Worked example 1: solution

total q = melt + warm
given: 30 g ice at 0 °C → liquid water at 25 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C
Step 1 · Identify each segment Step 2 · Compute each piece
melt: 30 g × 335 J1 g = 10,050 J · warm: 30 g × 4.184 J1 g·°C × 25 °C = 3138 J
Dr. Karmach

Worked example 1: solution

total q = melt + warm
given: 30 g ice at 0 °C → liquid water at 25 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C
Step 1 · Identify each segment Step 2 · Compute each piece
melt: 30 g × 335 J1 g = 10,050 J · warm: 30 g × 4.184 J1 g·°C × 25 °C = 3138 J
Step 3 · Add every piece
q = 10,050 J + 3138 J = 13,188 J
Melting alone costs 10,050 J, more than warming the liquid 25 °C. The flat step costs more. ✓
Dr. Karmach

Worked example 1: the route on the curve

total q = melt + warm
given: 30 g ice at 0 °C → liquid water at 25 °C · found: q = 13,188 J

The ice starts on the plateau, so no ice warms. Two pieces: melt, then warm water. ✓
Dr. Karmach

Worked example 2: melt, then warm to 40 °C

total q = melt + warm
given: 45 g ice at 0 °C → liquid water at 40 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C · wanted: q

A 45 g block of ice at 0 °C is melted and then warmed to 40 °C.

A common first attempt: the sample ends 40 °C warmer, so multiply the melting heat by 40 as well. Test it.

Dr. Karmach

Worked example 2: the melting step

total q = melt + warm
given: 45 g ice at 0 °C → liquid water at 40 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C

A common first attempt

melt: 45 g × 335 J1 g × 40 °C = 603,000 J ✗

Melting happens at a constant 0 °C. There is no temperature change to multiply, so ΔHfus already gives the whole melting heat.

Dr. Karmach

Worked example 2: the melting step

total q = melt + warm
given: 45 g ice at 0 °C → liquid water at 40 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C
A common first attempt
melt: 45 g × 335 J1 g × 40 °C = 603,000 J ✗
Step 1 · Identify each segment

Two pieces: melt at 0 °C, then warm the liquid from 0 °C to 40 °C. Only the warming piece has a ΔT.

The melting step holds at 0 °C, so it carries no temperature change. Only the warming step does. ✓
Dr. Karmach

Worked example 2: the two pieces

total q = melt + warm
given: 45 g ice at 0 °C → liquid water at 40 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C

Step 2 · Compute each piece

melt: 45 g × 335 J1 g = 15,075 J · warm: 45 g × 4.184 J1 g·°C × 40 °C = 7531.2 J
Dr. Karmach

Worked example 2: the two pieces

total q = melt + warm
given: 45 g ice at 0 °C → liquid water at 40 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C
Step 2 · Compute each piece
melt: 45 g × 335 J1 g = 15,075 J · warm: 45 g × 4.184 J1 g·°C × 40 °C = 7531.2 J
Step 3 · Add every piece
q = 15,075 J + 7531.2 J = 22,606 J
The two pieces add to 22,606 J. The plateau-times-ΔT shortcut, 603,000 J, was about 27 times too large. ✓
Dr. Karmach

Worked example 2: the route on the curve

total q = melt + warm
given: 45 g ice at 0 °C → liquid water at 40 °C · found: q = 22,606 J

The same two pieces. Only the slope carries a ΔT; the plateau is m·ΔHfus alone. ✓
Dr. Karmach

Take-home: a plateau is not q = m·c·ΔT

melt at 0 °C: correct
q = m · ΔHfus = 45 g × 335 J/g = 15,075 J · temperature stays 0 °C
treating the plateau as q = m·c·ΔT: wrong
45 g × 335 J/g × 40 °C = 603,000 J ✗ · there is no ΔT on a plateau

On a flat plateau the temperature is constant, so ΔT is zero. The heat comes from ΔHfus or ΔHvap. A phase-change energy is never multiplied by a temperature change.

Dr. Karmach

Worked example 3: ice at −20 °C to steam at 120 °C

total q = warm ice + melt + warm water + boil + warm steam
given: 20 g · −20 °C → 120 °C · c(ice) 2.03 · c(water) 4.184 · c(steam) 1.9 J/g·°C · ΔHfus 335 · ΔHvap 2259 J/g · wanted: q

A 20 g sample starts as ice at −20 °C and ends as steam at 120 °C.

Count the segments between the start and end, then compute and add each one.

Dr. Karmach

Worked example 3: warming and melting

total q = warm ice + melt + warm water + boil + warm steam
20 g · −20 °C → 120 °C · five segments to cross

Step 1 · Identify each segment

Five pieces: warm ice (−20 → 0), melt at 0 °C, warm water (0 → 100), boil at 100 °C, warm steam (100 → 120). Three slopes and two plateaus.

Dr. Karmach

Worked example 3: warming and melting

total q = warm ice + melt + warm water + boil + warm steam
20 g · −20 °C → 120 °C · five segments to cross
Step 1 · Identify each segment Step 2 · Compute each piece
warm ice: 20 g × 2.03 J1 g·°C × 20 °C = 812 J · melt: 20 g × 335 J1 g = 6700 J
warm water: 20 g × 4.184 J1 g·°C × 100 °C = 8368 J
Each slope uses its own phase's c: ice 2.03, water 4.184. The plateaus still to come cost more. ✓
Dr. Karmach

Worked example 3: boiling, then the total

total q = warm ice + melt + warm water + boil + warm steam
warm ice 812 · melt 6700 · warm water 8368 J so far

Step 2 · Compute each piece

boil: 20 g × 2259 J1 g = 45,180 J · warm steam: 20 g × 1.9 J1 g·°C × 20 °C = 760 J
Dr. Karmach

Worked example 3: boiling, then the total

total q = warm ice + melt + warm water + boil + warm steam
warm ice 812 · melt 6700 · warm water 8368 J so far
Step 2 · Compute each piece
boil: 20 g × 2259 J1 g = 45,180 J · warm steam: 20 g × 1.9 J1 g·°C × 20 °C = 760 J
Step 3 · Add every piece
q = 812 + 6700 + 8368 + 45,180 + 760 = 61,820 J
Boiling alone is 45,180 J, about three-quarters of the total. Vaporizing water takes the most heat. ✓
Dr. Karmach

Worked example 3: the route on the curve

total q = warm ice + melt + warm water + boil + warm steam
given: 20 g ice at −20 °C → steam at 120 °C · found: q = 61,820 J

The whole curve: three slopes, each with its own c, and both plateaus. ✓
Dr. Karmach

Plateau heats per mole

q = n · ΔH
n = mass ÷ 18.02 g/mol · ΔHfus = 6.02 kJ/mol · ΔHvap = 40.7 kJ/mol
slopes give J · a per-mole plateau gives kJ
1 kJ = 1000 J · every piece goes into one unit before adding

Plateau heats also come per mole. Grams convert to moles first, and that piece comes out in kilojoules. The slopes still give joules.

Dr. Karmach

Worked example 4: boil, then warm the steam

total q = boil + warm steam
given: 36.0 g water at 100.0 °C → steam at 130.0 °C · ΔHvap = 40.7 kJ/mol · c(steam) = 1.9 J/g·°C · 18.02 g/mol · wanted: q in kJ

36.0 g of water sits at its boiling point, 100.0 °C. It boils completely, and the steam warms to 130.0 °C. How much heat does it take, in kJ?

The heat of vaporization is given per mole.

Dr. Karmach

Worked example 4: solution

total q = boil + warm steam
given: 36.0 g water at 100.0 °C → steam at 130.0 °C · ΔHvap = 40.7 kJ/mol · c(steam) = 1.9 J/g·°C · 18.02 g/mol

Step 1 · Identify each segment

Two pieces: boil at 100.0 °C, then warm the steam to 130.0 °C. The water starts at its boiling point, so no liquid warms.

Dr. Karmach

Worked example 4: solution

total q = boil + warm steam
given: 36.0 g water at 100.0 °C → steam at 130.0 °C · ΔHvap = 40.7 kJ/mol · c(steam) = 1.9 J/g·°C · 18.02 g/mol
Step 1 · Identify each segment Step 2 · Compute each piece
boil: 36.0 g × 1 mol18.02 g × 40.7 kJ1 mol = 81.3 kJ
warm steam: 36.0 g × 1.9 J1 g·°C × 30.0 °C = 2052 J
Grams became moles before ΔHvap applied. The plateau came out in kJ, the slope in J. ✓
Dr. Karmach

Worked example 4: adding the pieces

total q = boil + warm steam
boil 81.3 kJ · warm steam 2052 J · wanted: q in kJ

A common first attempt

81.3 + 2052 = 2133 ✗

The two numbers carry different units. Kilojoules and joules do not add as they stand.

Dr. Karmach

Worked example 4: adding the pieces

total q = boil + warm steam
boil 81.3 kJ · warm steam 2052 J · wanted: q in kJ
A common first attempt
81.3 + 2052 = 2133 ✗
Step 3 · Add every piece
2052 J × 1 kJ1000 J = 2.052 kJ · q = 81.3 kJ + 2.052 kJ = 83.4 kJ
Boiling carries almost all of it: 81.3 of the 83.4 kJ. ✓
Dr. Karmach

Worked example 4: the route on the curve

total q = boil + warm steam
given: 36.0 g water at 100.0 °C → steam at 130.0 °C · found: q = 83.4 kJ

The per-mole plateau adds two moves: grams to moles, then kJ and J into one unit. ✓
Dr. Karmach

Your turn: 15 g of ice to warm water

total q = melt + warm
given: 15 g ice at 0 °C → liquid water at 50 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C
melt: 15 g × ( J / 1 g) = J · warm: 15 g × 4.184 J/(g·°C) × °C = 3138 J

Fill in ΔHfus, the melt heat, and the temperature change, then add the two pieces.

Dr. Karmach

Your turn: 15 g of ice to warm water

total q = melt + warm
given: 15 g ice at 0 °C → liquid water at 50 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C
melt: 15 g × ( J / 1 g) = J · warm: 15 g × 4.184 J/(g·°C) × °C = 3138 J

Fill in ΔHfus, the melt heat, and the temperature change, then add the two pieces.

melt: 15 g × (335 J / 1 g) = 5025 J · warm: 15 g × 4.184 J/(g·°C) × 50 °C = 3138 J
total = 5025 J + 3138 J = 8163 J
The melt costs 5025 J, more than warming the liquid all the way to 50 °C. Melting is the larger step. ✓
Dr. Karmach

Where this goes wrong

reference: 30 g ice at 0 °C → liquid water at 25 °C
melt 10,050 J + warm 3138 J = 13,188 J · ΔHfus 335 · c(ice) 2.03 · c(water) 4.184 J/g·°C
Treating a plateau as q = m·c·ΔT. Multiplying the fusion heat by a ΔT, 45 g × 335 J/g × 40 °C = 603,000 J, invents heat. Melting holds at 0 °C, so 45 g × 335 J/g = 15,075 J, no ΔT.
Skipping the melting plateau. Warming the liquid only, 30 g × 4.184 J/g·°C × 25 °C = 3138 J, leaves the ice unmelted. Melting first costs another 10,050 J.
Stopping at the melting point. 30 g × 335 J/g = 10,050 J melts the ice but leaves it at 0 °C. Warming to 25 °C adds 3138 J.
Using the wrong phase's specific heat. Warming ice with water's 4.184, 20 g × 4.184 × 20 °C = 1673.6 J, overcharges it. Ice's c is 2.03: 20 g × 2.03 × 20 °C = 812 J.
Dr. Karmach

Practice 2

total q = melt + warm
given: 20.0 g ice at 0 °C → liquid water at 30.0 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C · wanted: q

A 20.0 g block of ice at 0 °C is melted and warmed to 30.0 °C. How much heat, in J, does it take?

  1. 2.51 × 10³
  2. 6.70 × 10³
  3. 9.21 × 10³
  4. 2.01 × 10⁵
Dr. Karmach

Practice 2 answer: C

total q = melt + warm
given: 20.0 g ice at 0 °C → liquid water at 30.0 °C · ΔHfus = 335 J/g · c(water) = 4.184 J/g·°C
melt: 20.0 g × (335 J / 1 g) = 6.70 × 10³ J · warm: 20.0 g × 4.184 J/(g·°C) × 30.0 °C = 2.51 × 10³ J
q = 6.70 × 10³ J + 2.51 × 10³ J = 9.21 × 10³ J · answer C

A skipped the melting plateau: 20.0 × 4.184 × 30.0 = 2.51 × 10³ J warms the liquid but never melts the ice. B stopped at the melting point: 20.0 × 335 = 6.70 × 10³ J leaves the water at 0 °C. D multiplied the plateau by a ΔT: 20.0 × 335 × 30.0 = 2.01 × 10⁵ J.

Melting and warming are two separate costs, so both add ✓
Dr. Karmach

Practice 2: the route on the curve

total q = melt + warm
given: 20.0 g ice at 0 °C → liquid water at 30.0 °C · found: q = 9.21 × 10³ J

Two pieces: the melting plateau, then the water slope up to 30.0 °C. ✓
Dr. Karmach

Practice 3

total q = melt + warm
given: 72.1 g ice at 0 °C → liquid water at 20.0 °C · ΔHfus = 6.02 kJ/mol · c(water) = 4.184 J/g·°C · 18.02 g/mol · wanted: q in kJ

A cooler bag holds 72.1 g of ice at 0 °C. What heat, in kJ, turns it into liquid water at 20.0 °C?

  1. 4.40 × 10²
  2. 30.1
  3. 24.1
  4. 6.06 × 10³
Dr. Karmach

Practice 3 answer: B

total q = melt + warm
72.1 g ice, 0 °C → water, 20.0 °C · ΔHfus 6.02 kJ/mol · c(water) 4.184 J/g·°C · 18.02 g/mol
melt: 72.1 g × 1 mol18.02 g × 6.02 kJ1 mol = 24.1 kJ · warm: 72.1 × 4.184 × 20.0 = 6033 J = 6.03 kJ
q = 24.1 kJ + 6.03 kJ = 30.1 kJ · answer B

A used grams as moles: 72.1 × 6.02 + 6.03 = 4.40 × 10². C stopped at the melting point: 24.1 kJ leaves the water at 0 °C. D added J to kJ as they stand: 24.1 + 6033 = 6.06 × 10³.

72.1 g is 4.00 mol, so the melt is about 24 kJ. The warming adds a quarter more. ✓
Dr. Karmach

Practice 3: the route on the curve

total q = melt + warm
given: 72.1 g ice at 0 °C → liquid water at 20.0 °C · found: q = 30.1 kJ

The plateau per mole gives kJ, the slope gives J. One unit before adding. ✓
Dr. Karmach

Practice 4

total q = cool steam + condense + cool water
given: 10.0 g steam at 115 °C → liquid water at 70.0 °C · c(steam) 1.9 · c(water) 4.184 J/g·°C · ΔHvap 2259 J/g · wanted: q, signed

A 10.0 g sample of steam at 115 °C cools, condenses, and ends as liquid water at 70.0 °C. What is q for the sample, in J?

  1. +2.41 × 10⁴
  2. −1.54 × 10³
  3. −2.29 × 10⁴
  4. −2.41 × 10⁴
Dr. Karmach

Practice 4 answer: D

total q = cool steam + condense + cool water
given: 10.0 g · 115 °C → 70.0 °C · c(steam) 1.9 · c(water) 4.184 J/g·°C · ΔHvap 2259 J/g · ΔT = Tfinal − Tinitial
cool steam: 10.0 g × 1.9 × (100 − 115) °C = −285 J · condense: −(10.0 g × 2259 J/g) = −22,590 J · cool water: 10.0 g × 4.184 × (70.0 − 100) °C = −1255 J
q = −285 J + (−22,590 J) + (−1255 J) = −24,130 J = −2.41 × 10⁴ J · answer D

A lost the sign: a cooling path releases heat, so q is negative. B skipped the condensation plateau: −285 − 1255 = −1.54 × 10³ J. C stopped at 100 °C: −285 − 22,590 = −2.29 × 10⁴ J.

Heating curve run backward: every step is negative, condensing dominates ✓
Dr. Karmach

Practice 4: the route on the curve

total q = cool steam + condense + cool water
given: 10.0 g steam at 115 °C → liquid water at 70.0 °C · found: q = −2.41 × 10⁴ J

A cooling path runs the curve backward. Every piece releases heat: each q is negative. ✓
Dr. Karmach

Practice 5

total q = the sum of every segment crossed
given: 27.0 g ice at −12.0 °C → liquid water at 35.0 °C · c(ice) 2.03 · c(water) 4.184 J/g·°C · ΔHfus 6.02 kJ/mol · 18.02 g/mol · wanted: q in J

A 27.0 g ice cube at −12.0 °C is heated until it is liquid water at 35.0 °C. What heat, in J, does it absorb?

  1. 1.30 × 10⁴
  2. 4.61 × 10³
  3. 1.43 × 10⁴
  4. 9.68 × 10³
  5. 1.36 × 10⁴
Dr. Karmach

Practice 5 answer: E

given: 27.0 g ice, −12.0 °C → water, 35.0 °C · c(ice) 2.03 · c(water) 4.184 J/g·°C · ΔHfus 6.02 kJ/mol · 18.02 g/mol
warm ice: 27.0 × 2.03 × 12.0 = 658 J · warm water: 27.0 × 4.184 × 35.0 = 3954 J
melt: 27.0 g × 1 mol18.02 g × 6.02 kJ1 mol = 9020 J · q = 658 + 9020 + 3954 = 1.36 × 10⁴ J · answer E

A skipped the ice leg: 9020 + 3954 = 1.30 × 10⁴. B skipped the melt: 658 + 3954 = 4.61 × 10³. C used c(water) on ice: 1356 + 9020 + 3954 = 1.43 × 10⁴. D stopped at 0 °C: 658 + 9020 = 9.68 × 10³.

The melt, 9.02 kJ = 9020 J, is two-thirds of the total. ✓
Dr. Karmach

Practice 5: the route on the curve

total q = warm ice + melt + warm water
given: 27.0 g ice at −12.0 °C → liquid water at 35.0 °C · found: q = 1.36 × 10⁴ J

Two slopes and the per-mole plateau between them. Its kJ became J before the sum. ✓
Dr. Karmach

Check yourself

  1. A path crosses a flat plateau, then a rising slope. Which equation does each part use? Why does the plateau carry no ΔT?
  2. Water at 100 °C and steam at 100 °C are the same temperature. Why does boiling the water still take heat?

The plateaus are long because melting and boiling pull particles apart. How hard the particles hold on differs from solid to solid: ionic, metallic, molecular, and network solids melt at very different temperatures.

Dr. Karmach

7 · Types of Solids

Classify a solid as crystalline or amorphous and, for a crystal, sort it into one of the four types (ionic, metallic, covalent-network, molecular) from the particle at its lattice points and the force holding them, then predict its melting point, hardness, and conductivity.

Dr. Karmach

Four solids, four melting points

Ice melts at 0 °C. Diamond stays solid until about 3550 °C. The particles inside each solid, and what holds them together, set the difference.

Dr. Karmach

Crystalline vs amorphous

A crystalline solid has a regular, repeating lattice, so it melts sharply at one temperature. An amorphous solid has no long-range order; heated, it softens gradually over a range.

crystalline = ordered, repeating lattice → sharp melting point
amorphous = no long-range order → softens over a range · glass, rubber, most plastics
Dr. Karmach

What holds a solid together

A solid holds its particles in fixed positions. A force keeps them there, and melting must overcome it. That force is one of the three intermolecular forces or one of three kinds of bond.

between separate molecules: intermolecular forces
dispersion · dipole-dipole · hydrogen bonding · weak: a molecular solid melts low
through the whole crystal: bonds
ionic bonds · metallic bonding · covalent bonds · ionic and network solids melt high · metals vary
Dr. Karmach

Two questions sort every crystal

Two answers classify a crystalline solid: the particle at each lattice point, and the force holding those particles. The force sets the properties: stronger force, higher melting point, harder solid.

particle + force → type → properties
ionic · metallic · covalent network · molecular
memory hook: metal only, metallic · metal with nonmetal, ionic · nonmetals only, molecular
except the short network list: C (diamond, graphite), Si, SiO₂, SiC · a polyatomic ion also means ionic (NH₄Cl)
Dr. Karmach

Ionic & metallic solids

Ionic: positive & negative ions · electrostatic ionic bonds
high mp, hard but brittle; conducts only when molten or dissolved · NaCl, MgO
Metallic: metal cations in a sea of shared electrons · metallic bonding
melting point varies, malleable & ductile; conducts as a solid · Cu, Fe, Au

The mobile sea of electrons lets a metal bend without shattering and carry a current.

memory hook: metal electrons are already free · ions must be set free
a metal conducts as a solid · an ionic solid conducts only once melted or dissolved
Dr. Karmach

Covalent-network & molecular solids

Covalent network: atoms joined in one continuous covalent network
very high mp, very hard, usually nonconducting · diamond, SiO₂ (quartz), SiC
Molecular: whole molecules held by intermolecular forces
low mp, soft, nonconducting · ice, dry ice (CO₂), sugar · solid argon sorts here too: lone atoms held by dispersion

Graphite is the exception among network solids: its sheets slide (soft, a lubricant), and its delocalized electrons conduct.

Dr. Karmach

The whole picture

Read any row across: the particle sets the force, and the force sets every property.

Dr. Karmach

Classify a solid in three steps

  1. Name the particle: ions, metal atoms, network atoms, or molecules.
  2. Name the force: ionic, metallic, covalent network, or intermolecular.
  3. Predict the properties from that force: melting point, hardness, conductivity.

Dr. Karmach

Guided example: hydrogen chloride

HCl(s): hydrogen chloride, frozen
given: the formula HCl · wanted: the solid type, its strongest force, its properties

Hydrogen chloride is a gas at room temperature. Cooled far enough, it freezes into a crystal. Classify solid HCl, then predict its properties.

Step 1 asks the formula questions in order: metal only? A metal or NH₄⁺ with a nonmetal? On the network list?

Dr. Karmach

Guided example: name the particle

HCl(s): hydrogen chloride, frozen
given: the formula HCl · wanted: type, strongest force, properties

Step 1 · Name the particle

move 1 · metal only? no
H sits above the group 1 metals, but hydrogen is a nonmetal
Dr. Karmach

Guided example: name the particle

HCl(s): hydrogen chloride, frozen
given: the formula HCl · wanted: type, strongest force, properties

Step 1 · Name the particle

move 1 · metal only? no
H sits above the group 1 metals, but hydrogen is a nonmetal
move 2 · a metal or NH₄⁺ with a nonmetal? no
no metal, no NH₄⁺ · H and Cl share electrons: no ions
Dr. Karmach

Guided example: name the particle

HCl(s): hydrogen chloride, frozen
given: the formula HCl · wanted: type, strongest force, properties

Step 1 · Name the particle

move 1 · metal only? no
H sits above the group 1 metals, but hydrogen is a nonmetal
move 2 · a metal or NH₄⁺ with a nonmetal? no
no metal, no NH₄⁺ · H and Cl share electrons: no ions
move 3 · on the network list? no
not C, Si, SiO₂, or SiC · particle: the HCl molecule → a molecular solid
Dr. Karmach

Guided example: name the particle

HCl(s): hydrogen chloride, frozen
given: the formula HCl · wanted: type, strongest force, properties

Step 1 · Name the particle

move 1 · metal only? no
H sits above the group 1 metals, but hydrogen is a nonmetal
move 2 · a metal or NH₄⁺ with a nonmetal? no
no metal, no NH₄⁺ · H and Cl share electrons: no ions
move 3 · on the network list? no
not C, Si, SiO₂, or SiC · particle: the HCl molecule → a molecular solid
Three no answers leave one type. Each HCl unit is a separate molecule. ✓
Dr. Karmach

Guided example: force and properties

HCl(s): a molecular solid
particle: HCl molecules · wanted: strongest force, properties

Step 2 · Name the force

Cl pulls the shared electrons harder than H does. The H–Cl bond is polar, so the molecule is polar.

polar molecule · H bonded to Cl, not to N, O, or F → dipole-dipole, plus dispersion
Dr. Karmach

Guided example: force and properties

HCl(s): a molecular solid
particle: HCl molecules · wanted: strongest force, properties
Step 2 · Name the force
polar molecule · H bonded to Cl, not to N, O, or F → dipole-dipole, plus dispersion
Step 3 · Predict the properties
intermolecular forces only → low melting point · soft · nonconducting
Solid HCl melts at −114 °C, 114 °C below ice. Its molecules carry no net charge, so the solid does not conduct. ✓
Dr. Karmach

Guided example: the route on the map

HCl(s): molecular solid · dipole-dipole
metal only? no · metal or NH₄⁺? no · network list? no · polar, no H on N, O, or F

The formula row alone found the type. No melting point or conductivity test was needed. ✓
Dr. Karmach

Worked example 1: calcium chloride

CaCl₂: a road de-icer
Ca is a metal · Cl is a nonmetal · wanted: the solid type, then its melting point, hardness, and conductivity

Classify solid calcium chloride, then predict its properties.

Dr. Karmach

Worked example 1: solution

CaCl₂: a road de-icer
Ca is a metal · Cl is a nonmetal

Step 1 · Name the particle

A metal with a nonmetal gives ions: one Ca²⁺ for every two Cl⁻, so +2 + 2(−1) = 0.

Dr. Karmach

Worked example 1: solution

CaCl₂: a road de-icer
Ca is a metal · Cl is a nonmetal
Step 1 · Name the particle Step 2 · Name the force
Ca²⁺ and Cl⁻ ions → ionic bonds → ionic solid
Dr. Karmach

Worked example 1: solution

CaCl₂: a road de-icer
Ca is a metal · Cl is a nonmetal
Step 1 · Name the particle Step 2 · Name the force
Ca²⁺ and Cl⁻ ions → ionic bonds → ionic solid
Step 3 · Predict the properties
ionic solid → high melting point · hard but brittle · conducts only when molten or dissolved
CaCl₂ melts at 772 °C, near table salt's 801 °C. Dissolved on a road, its free ions conduct. ✓
Dr. Karmach

Worked example 1: the route on the map

CaCl₂: an ionic solid
metal only? no, Cl is a nonmetal · a metal or NH₄⁺ with a nonmetal? yes, Ca with Cl

The second question answered yes. The network list never came up. ✓
Dr. Karmach

Worked example 2: an unknown shiny solid

unknown solid: shiny, melts at 1085 °C
bends without breaking · conducts electricity as a solid · wanted: its type and the particle feature behind it

Only the properties are known. Work the three steps from this evidence.

Dr. Karmach

Worked example 2: solution

unknown solid: shiny, melts at 1085 °C
bends without breaking · conducts as a solid

Step 1 · Name the particle

Shiny, bendable, and conducting as a solid: only a metal fits all three. Its lattice holds metal cations in a sea of mobile electrons.

Dr. Karmach

Worked example 2: solution

unknown solid: shiny, melts at 1085 °C
bends without breaking · conducts as a solid
Step 1 · Name the particle Step 2 · Name the force
cations + mobile electrons → metallic bonding → metallic solid
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Worked example 2: solution

unknown solid: shiny, melts at 1085 °C
bends without breaking · conducts as a solid
Step 1 · Name the particle Step 2 · Name the force
cations + mobile electrons → metallic bonding → metallic solid
Step 3 · Predict the properties
metallic: shiny · malleable · conducts as a solid · mp varies
every observed property matches · this is copper
NaCl answers the conductivity test the other way. Its ions stay locked in the lattice, so it conducts only once melted or dissolved. ✓
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Worked example 2: the route on the map

unknown shiny solid: a metallic solid
no formula given · conducts as a solid? yes

Only properties were known, so the bottom row sorted it. One yes settled it. ✓
Dr. Karmach

Your turn: iodine

I₂: a nonmetal element built of I₂ molecules
nonpolar molecule · wanted: the particle, the force, the properties
step solid iodine
1 · name the particle
2 · name the force
3 · predict the properties melting point, soft,

Fill the blanks. Iodine and diamond are both nonmetal elements; check the network list.

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Your turn: iodine

I₂: a nonmetal element built of I₂ molecules
nonpolar molecule · wanted: the particle, the force, the properties
step solid iodine
1 · name the particle
2 · name the force
3 · predict the properties melting point, soft,

Fill the blanks. Iodine and diamond are both nonmetal elements; check the network list.

I₂ → molecular solid
particle: I₂ molecules · force: dispersion (intermolecular) · low mp (114 °C), soft, nonconducting
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Where this goes wrong

Ionic solids conduct as solids. They do not. The ions are locked in place. An ionic solid conducts only once molten or dissolved, when the ions can move.
Dry ice is a network solid like SiO₂. No. CO₂ freezes as a molecular solid: discrete molecules, weak forces, sublimes at −78 °C. SiO₂ is a covalent network that melts near 1700 °C.
A wide melting range means crystalline. Backwards. A sharp melting point marks a crystal. Softening over a range marks an amorphous solid.
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Practice 1

Ni · NiO · Si · S₈
nickel · nickel(II) oxide · silicon · sulfur

Which of these forms a metallic solid?

  1. Ni
  2. NiO
  3. Si
  4. S₈
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Practice 1 answer: A

Ni: metal atoms only → metallic solid, answer A

B contains a metal, but Ni with O is a metal with a nonmetal: ionic. C is shiny and gray, but silicon is on the network list: a covalent network. D is a single element, but sulfur is a nonmetal: S₈ molecules make a molecular solid.

A metallic solid holds metal atoms and nothing else. Nickel is the only choice with no nonmetal in it. ✓
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Practice 1: the route on the map

Ni · NiO · Si · S₈
Ni: metal only · NiO: metal with O · Si: network list · S₈: molecules, nonpolar

Four formulas leave by four exits. Only Ni stops at the first question. ✓
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Practice 2

an unknown colorless solid
extremely hard · melts near 2000 °C · does not conduct as a solid or when molten

Which type of solid is it?

  1. Ionic: hard, with a very high melting point, like most salts
  2. Metallic: only a metal stays solid past 1000 °C
  3. Covalent network: hard, very high melting point, no ions to carry current
  4. Molecular: it does not conduct, so it must be built of molecules
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Practice 2 answer: C

extremely hard · very high mp · no conduction, solid or molten → covalent network, answer C

A matched hardness and melting point but skipped the molten test: a melted ionic solid conducts. B ignored the conductivity; a metal conducts as a solid. D read only the conductivity; a molecular solid melts low and is soft, never near 2000 °C.

Quartz and silicon carbide fit this profile. The whole crystal is one covalent network, so melting means breaking covalent bonds. ✓
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Practice 2: the route on the map

the colorless solid: covalent network
conducts as a solid? no · melted? no · very hard, very high mp? yes

No formula was given, so the property row did the sorting. Three questions were needed. ✓
Dr. Karmach

Practice 3

ammonium nitrate, NH₄NO₃: a fertilizer
a white crystalline solid · wanted: the solid type and when it conducts

Which type of solid is ammonium nitrate, and when does it conduct?

  1. Molecular: only nonmetals, so it never conducts
  2. Ionic: conducts once melted or dissolved
  3. Covalent network: nonmetal atoms bonded throughout one crystal
  4. Ionic: conducts as a solid
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Practice 3 answer: B

NH₄⁺ and NO₃⁻ ions → ionic bonds → ionic solid, conducts once melted or dissolved, answer B

A applied the nonmetals-only rule without looking for a polyatomic ion. NH₄⁺ and NO₃⁻ carry charges, so the solid is built of ions. C picked a network solid, but the network list is short: C, Si, SiO₂, SiC. D named the right type but let the ions move in the solid; in the lattice they are locked in place.

Ammonium nitrate is a salt like NaCl. Dissolved in soil water, its ions move freely, and the solution conducts. ✓
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Practice 3: the route on the map

NH₄NO₃: an ionic solid
metal only? no · a metal or NH₄⁺ with a nonmetal? yes, NH₄⁺ with NO₃⁻

NH₄⁺ answers the second question just as a metal would. ✓
Dr. Karmach

Practice 4

urea, CO(NH₂)₂: a crystalline fertilizer
melts at 133 °C

What type of solid is urea, and what is the strongest force between its particles?

  1. Ionic · ionic bonds
  2. Covalent network · covalent bonds
  3. Molecular · dispersion
  4. Molecular · dipole-dipole
  5. Molecular · hydrogen bonding
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Practice 4 answer: E

nonmetals only · no NH₄⁺ · not on the network list → molecules · H bonded to N → molecular, hydrogen bonding, answer E

A read each NH₂ group as ammonium. NH₄⁺ carries 4 H and a charge; urea holds 2 × 2 = 4 H in two neutral NH₂ groups and no ion. B named the covalent bonds inside each molecule; melting separates whole molecules and breaks none of those bonds. C stopped at dispersion, the force every molecule has. D saw a polar molecule but missed H bonded to N.

No network solid melts near 133 °C. The heat separates whole urea molecules held by N–H hydrogen bonds. ✓
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Practice 4: the route on the map

CO(NH₂)₂: molecular · hydrogen bonding
metal only? no · metal or NH₄⁺? no · network list? no · H bonded to N

Three no answers reach molecular; the H on N picks the strongest force. ✓
Dr. Karmach

Practice 5

an unlabeled stockroom solid
soft enough to cut with a knife · melts at 98 °C · conducts electricity as a solid

What type of solid is it?

  1. Ionic
  2. Molecular (nonpolar)
  3. Molecular (polar)
  4. Metallic
  5. Covalent network
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Practice 5 answer: D

conducts as a solid? yes → metallic, answer D

Conductivity decides first. Softness and a 98 °C melting point fit a metal too: metallic melting points vary widely.

A let the ions move in the solid; an ionic solid conducts only once melted or dissolved. B let the softness and the low melting point outvote the conductivity. C read polarity as charge; polar molecules carry no net charge and never conduct. E reached for graphite, the one conducting network; graphite stays solid past 3500 °C.

This is sodium: soft, melting at 98 °C, conducting like any metal. ✓
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Practice 5: the route on the map

the 98 °C solid: metallic
conducts as a solid? yes · softness and melting point never enter the route

The first property question settles it. Softness and a low melting point do not rule out a metal. ✓
Dr. Karmach

Check yourself

  1. Diamond and dry ice are both built only from nonmetal atoms, yet diamond melts near 3550 °C while dry ice sublimes at −78 °C. Which is covalent network and which is molecular, and what force explains the gap?
  2. Sugar and table salt both dissolve in water, but only one solution conducts. Which one, and what does that say about each solid's particles?

Dissolved ions carry current; dissolved molecules do not. That difference runs through the solutions unit.

Dr. Karmach

Can you…?

  • ☐ name the six changes of state, label each endothermic or exothermic, and read a heating or cooling curve?
  • ☐ calculate the heat for warming steps with q = mcΔT and for phase changes with the heats of fusion and vaporization, and add them along a heating curve?
  • ☐ identify the intermolecular forces in a substance and rank substances by boiling point and vapor pressure?
  • ☐ explain vapor pressure, boiling point, surface tension, and viscosity from intermolecular forces, including why boiling point changes with outside pressure?
  • ☐ read a phase diagram: the stable phase at a given pressure and temperature, the triple point, and the normal melting and boiling points?
  • ☐ classify a solid as ionic, metallic, molecular, or network and predict its melting point, hardness, and conductivity?

If any box stays empty, the practice site has a drill for it. 🧪

Dr. Karmach