Acids & Bases

Preparation for General Chemistry · Dr. Karmach

Dr. Karmach

By the end of this unit, you can…

  • Recognize acids and bases by their properties and define them by the Arrhenius and Brønsted-Lowry definitions
  • Identify the Brønsted-Lowry acid, base, and conjugate pairs in a reaction, and write a species' conjugate acid or base
  • Classify acids and bases as strong or weak, write their ionization with the correct arrow, and predict the products of neutralization and gas-forming reactions
  • Use K_w, pH = −log[H₃O⁺], pOH, and pH + pOH = 14 to convert among [H₃O⁺], [OH⁻], pH, and pOH and label a solution acidic, basic, or neutral
  • Find an unknown acid or base concentration from titration data
Dr. Karmach

Today's route 🗺️

  1. Acids and Bases, Strong vs Weak
  2. Acids and Bases, Definitions and Neutralization
  3. The pH Scale
  4. Electrolytes & Dissociation
  5. Titration Calculations
Dr. Karmach

1 · Acids and Bases, Strong vs Weak

Classify any acid or base as strong or weak using the memorize-lists, write its ionization with the correct arrow (→ for full, ⇌ for partial), and predict the products of neutralization and gas-evolution reactions.

Dr. Karmach

Strong is not the same as a lot

Stomach acid is hydrochloric acid, HCl, a strong acid, yet dilute. Strong and weak describe how completely an acid ionizes, not how much of it is dissolved.

Dr. Karmach

Three reactions with an acid in them

Mg(s) + H₂SO₄(aq): bubbles
single displacement · the gas is H₂
Na₂CO₃(aq) + HCl(aq): bubbles
gas formation · washing soda meets hydrochloric acid
HNO₃(aq) + Ba(OH)₂(aq): no bubbles, the beaker warms
neutralization · an acid meets a base

In all three, the acid hands over H⁺. Strong and weak describe how completely an acid does that in plain water, before any partner is added.

Dr. Karmach

What makes something an acid or a base

Dissolved in water, an acid produces H⁺, carried as the hydronium ion H₃O⁺. A base produces OH⁻.

acid → H⁺ (H₃O⁺) in water · base → OH⁻ in water
Arrhenius definitions · Brønsted–Lowry widens them: an acid donates a proton (H⁺), a base accepts one

Every acid here has an H to release; every hydroxide carries its OH⁻.

Dr. Karmach

Strong vs weak = the degree of ionization

Strong means essentially every molecule ionizes; weak means a small fraction. The ⇌ arrow marks the reverse reaction: ions rejoin as fast as molecules split, so the mixture settles mostly intact.

HCl → H⁺ + Cl⁻ (≈100%, one → arrow) · CH₃COOH ⇌ H⁺ + CH₃COO⁻ (partial, ⇌)
strong = fully ionized = a strong electrolyte · weak = barely ionized = a weak electrolyte
Dr. Karmach

What a 1 M acid bottle contains

a bottle labeled 1 M HCl actually has no HCl in it, but 1 M H⁺(aq) and 1 M Cl⁻(aq)
strong acid: every molecule ionized · nothing left to match the label
a bottle labeled 1 M HA, where HA is a weak acid, actually has mostly HA in it and only a small amount of H⁺(aq) and A⁻(aq)
weak acid: the molecules survive · few ions

The label names what was dissolved. The strong or weak classification tells what the water holds now.

Dr. Karmach

The seven strong acids: memorize them

Only seven common acids are strong; everything not on the list is weak. The list is measured, not deduced: these seven ionize essentially completely in water.

HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ · HClO₃
3 hydrohalic (HCl, HBr, HI) + 4 oxoacids (HNO₃, H₂SO₄, HClO₄, HClO₃) = 3 + 4 = 7
not on it: CH₃COOH · HF · H₂CO₃ · H₃PO₄ → all weak, partial ionization (⇌)
the structural reason for the split waits for equilibrium
Dr. Karmach

Strong bases, and neutralization

The strong bases are the metal hydroxides that ionize completely: every group 1 hydroxide, plus the heavy group 2 hydroxides.

group 1: LiOH NaOH KOH RbOH CsOH · group 2 (heavy): Ca(OH)₂ Sr(OH)₂ Ba(OH)₂
5 + 3 = 8 strong bases · Ca(OH)₂ → Ca²⁺ + 2 OH⁻ releases 2 × 1 = 2 hydroxide ions · Ca(OH)₂ and Sr(OH)₂ barely dissolve (the chart says insoluble), but all that dissolves ionizes fully
NH₃ + H₂O ⇌ NH₄⁺ + OH⁻ · acid + base → salt + water
ammonia and amines make OH⁻ only partially: weak bases · an acid and a base neutralize to a salt plus water

Ammonia and the amines are weak bases. An acid and a base neutralize each other.

Dr. Karmach

The method

  1. Acid or base? An H to release: acid. Hydroxide or NH₃/amine: base.
  2. On a memorize list? Listed: strong. Not listed: weak.
  3. Pick the arrow. Strong ionizes fully: →. Weak, partially: ⇌.
  4. Ignore concentration. Strength is the fraction ionized.

Dr. Karmach

Guided example: lactic acid

HC₃H₅O₃ dissolved in water
given: lactic acid · wanted: strong or weak, and its ionization with the right arrow

Lactic acid sours milk and builds up in hard-working muscle. Classify it and write its ionization.

Each method step is one move. Name the step, then make the move.

Dr. Karmach

Guided example: classify

HC₃H₅O₃ dissolved in water
given: lactic acid · wanted: strong or weak, and its ionization

Step 1 · Acid or base?

HC₃H₅O₃: an H written first
move 1 · the H in front is the one it releases · answer: an acid
Dr. Karmach

Guided example: classify

HC₃H₅O₃ dissolved in water
given: lactic acid · wanted: strong or weak, and its ionization

Step 1 · Acid or base?

HC₃H₅O₃: an H written first
move 1 · the H in front is the one it releases · answer: an acid
Step 2 · On a memorize list?
HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ · HClO₃
move 2 · HC₃H₅O₃ is not among the seven · answer: weak
Dr. Karmach

Guided example: classify

HC₃H₅O₃ dissolved in water
given: lactic acid · wanted: strong or weak, and its ionization

Step 1 · Acid or base?

HC₃H₅O₃: an H written first
move 1 · the H in front is the one it releases · answer: an acid
Step 2 · On a memorize list?
HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ · HClO₃
move 2 · HC₃H₅O₃ is not among the seven · answer: weak
An acid, and off the list: a weak acid. The list decided it, not the look of the formula. ✓
Dr. Karmach

Guided example: write the ionization

HC₃H₅O₃ dissolved in water
classified: an acid, not among the seven → weak

Step 3 · Pick the arrow

HC₃H₅O₃(aq) ⇌ H⁺(aq) + C₃H₅O₃⁻(aq)
weak: ⇌ · H: 6 = 1 + 5 ✓ · C: 3 = 3 ✓ · O: 3 = 3 ✓ · charge: (1+) + (1−) = 0
Dr. Karmach

Guided example: write the ionization

HC₃H₅O₃ dissolved in water
classified: an acid, not among the seven → weak
Step 3 · Pick the arrow
HC₃H₅O₃(aq) ⇌ H⁺(aq) + C₃H₅O₃⁻(aq)
weak: ⇌ · H: 6 = 1 + 5 ✓ · C: 3 = 3 ✓ · O: 3 = 3 ✓ · charge: (1+) + (1−) = 0
Step 4 · Ignore concentration

Sour milk or a 1 M lab bottle: most lactic acid molecules stay whole in both. Concentration never enters the call.

Dr. Karmach

Guided example: write the ionization

HC₃H₅O₃ dissolved in water
classified: an acid, not among the seven → weak
Step 3 · Pick the arrow
HC₃H₅O₃(aq) ⇌ H⁺(aq) + C₃H₅O₃⁻(aq)
weak: ⇌ · H: 6 = 1 + 5 ✓ · C: 3 = 3 ✓ · O: 3 = 3 ✓ · charge: (1+) + (1−) = 0
Step 4 · Ignore concentration
Four named steps, four moves: acid, off the list, ⇌, concentration ignored. Only a small fraction of the molecules release H⁺. ✓
Dr. Karmach

Guided example: the route on the chart

HC₃H₅O₃(aq) ⇌ H⁺(aq) + C₃H₅O₃⁻(aq)
acid: yes · one of the seven: no · found: weak acid, ⇌

One branch and one list check. The base questions never came up. ✓
Dr. Karmach

Worked example 1: classify three species

HNO₃ · HF · Ca(OH)₂
for each: strong or weak? which electrolyte? which arrow: → or ⇌?

Nitric acid, hydrofluoric acid, and calcium hydroxide. Check each against the memorize-lists, then write how it behaves in water.

Dr. Karmach

Worked example 1: solution

HNO₃ · on the strong-acid list

HNO₃ is one of the seven strong acids, so it ionizes completely: a strong electrolyte.

HNO₃ → H⁺ + NO₃⁻
full ionization, single → arrow · 1 + 1 = 2 ions per formula unit
Dr. Karmach

Worked example 1: solution

HNO₃ · on the strong-acid list

HNO₃ → H⁺ + NO₃⁻
full ionization, single → arrow · 1 + 1 = 2 ions per formula unit
HF · not on the list → weak

HF is not one of the seven, so it is a weak acid: a weak electrolyte, partial ionization.

HF ⇌ H⁺ + F⁻
mostly intact HF molecules · the ⇌ arrow marks partial ionization
Dr. Karmach

Worked example 1: solution

HNO₃ · on the strong-acid list

HNO₃ → H⁺ + NO₃⁻
full ionization, single → arrow · 1 + 1 = 2 ions per formula unit
HF · not on the list → weak
HF ⇌ H⁺ + F⁻
mostly intact HF molecules · the ⇌ arrow marks partial ionization
Ca(OH)₂ · a heavy group 2 hydroxide → strong base
Ca(OH)₂ → Ca²⁺ + 2 OH⁻
strong base, strong electrolyte · 1 + 2 = 3 ions, of which 2 × 1 = 2 are OH⁻
Dr. Karmach

Worked example 1: solution

HNO₃ · on the strong-acid list

HNO₃ → H⁺ + NO₃⁻
full ionization, single → arrow · 1 + 1 = 2 ions per formula unit
HF · not on the list → weak
HF ⇌ H⁺ + F⁻
mostly intact HF molecules · the ⇌ arrow marks partial ionization
Ca(OH)₂ · a heavy group 2 hydroxide → strong base
Ca(OH)₂ → Ca²⁺ + 2 OH⁻
strong base, strong electrolyte · 1 + 2 = 3 ions, of which 2 × 1 = 2 are OH⁻
On the lists, HNO₃ and Ca(OH)₂ ionize fully (→); HF is off the list, mostly intact (⇌).
Dr. Karmach

Worked example 1: the route on the chart

HNO₃ → H⁺ + NO₃⁻ · HF ⇌ H⁺ + F⁻ · Ca(OH)₂ → Ca²⁺ + 2 OH⁻
HNO₃: acid, one of the seven · HF: acid, not one of the seven · Ca(OH)₂: base, a strong base

Three formulas leave by three exits. Only the two lists decided strong or weak. ✓
Dr. Karmach

Where this goes wrong

"HF is strong because F is so electronegative." Electronegativity does not decide it: HF is simply not on the list of seven, so it is weak (⇌).
"Concentrated means strong." Concentration is amount dissolved; strength is the fraction ionized. 10 M acetic acid is still weak; 0.01 M HCl is still strong.
Sulfuric ↔ acetic mix-up. H₂SO₄ is on the list (strong, →); acetic acid CH₃COOH is not (weak, ⇌). Being an acid does not make it strong.
"NH₃ can't be a base: it has no OH." It makes OH⁻ by pulling H⁺ off water: NH₃ + H₂O ⇌ NH₄⁺ + OH⁻: a weak base.
Dr. Karmach

Practice 1: spot the exception

Three of these ionize essentially 100% in water. Which one is not a strong acid?

  1. HClO₄
  2. HCl
  3. HClO
  4. HNO₃
Dr. Karmach

Practice 1: answer C

HClO ⇌ H⁺ + ClO⁻: a weak acid (answer C)
HClO (hypochlorous) is not among the seven; HClO₄, HCl, HNO₃ all are

Watch the chlorine oxoacids: HClO₄ (perchloric) and HClO₃ (chloric) are on the strong list, but HClO (hypochlorous) is weak: it ionizes only partially (⇌). HCl and HNO₃ are strong (→).

Two fewer oxygens separate HClO₃, strong, from HClO, weak. Classify from the list, not from the look of the formula.
Dr. Karmach

Practice 1: the route on the chart

HClO ⇌ H⁺ + ClO⁻ (answer C)
all four: acids · HClO₄, HCl, HNO₃: one of the seven · HClO: not one of the seven

All four take the acid branch. The list check splits them: three strong exits, one weak. ✓
Dr. Karmach

Practice 2: label four species

HClO₃ · HCOOH · Ba(OH)₂ · C₂H₅NH₂
chloric acid · formic acid · barium hydroxide · ethylamine

Which labels, in order, fit the four species in water?

  1. strong acid · weak acid · weak base · weak base
  2. weak acid · weak acid · strong base · weak base
  3. strong acid · weak base · strong base · weak base
  4. strong acid · weak acid · strong base · weak acid
  5. strong acid · weak acid · strong base · weak base
Dr. Karmach

Practice 2: answer E

HClO₃ → H⁺ + ClO₃⁻ · HCOOH ⇌ H⁺ + HCOO⁻
HClO₃: one of the seven, strong acid · HCOOH: the H of –COOH leaves, off the list, weak acid
Ba(OH)₂ → Ba²⁺ + 2 OH⁻ · C₂H₅NH₂ + H₂O ⇌ C₂H₅NH₃⁺ + OH⁻ (answer E)
Ba(OH)₂: heavy group 2 hydroxide, strong base, (2+) + 2(1−) = 0 · ethylamine: an amine, weak base, H: 7 + 2 = 9 = 8 + 1 ✓

A stopped the strong-base list at group 1; the heavy group 2 hydroxides, Ba(OH)₂ among them, ionize fully too. B mixed up chloric acid HClO₃ with hypochlorous acid HClO. C read the OH inside –COOH as hydroxide. D counted an amine's H atoms as acidic; its nitrogen takes H⁺ from water.

Every call came from a list or a formula feature. The strong-base list runs past group 1. ✓
Dr. Karmach

Practice 2: the route on the chart

HClO₃ · HCOOH · Ba(OH)₂ · C₂H₅NH₂ (answer E)
two acids: one on the list, one off · two bases: one on the list, one amine

Four species leave by all four exits. Each took exactly two questions. ✓
Dr. Karmach

Worked example 2: predict and balance a neutralization

H₃PO₄(aq) + Ca(OH)₂(aq) → ?
acid + base → salt + water · wanted: the products and the coefficients

Phosphoric acid meets calcium hydroxide. One HCl releases one H⁺: monoprotic. H₂SO₄ releases two: diprotic. H₃PO₄ releases three: triprotic. Predict both products, then balance.

Dr. Karmach

Worked example 2: the products

H₃PO₄(aq) + Ca(OH)₂(aq) → ?
wanted: the products and the coefficients

Predict the products

The salt pairs Ca²⁺ with PO₄³⁻; charge balance builds Ca₃(PO₄)₂. The other product of every neutralization is water.

Dr. Karmach

Worked example 2: the products

H₃PO₄(aq) + Ca(OH)₂(aq) → ?
wanted: the products and the coefficients

Predict the products

The salt pairs Ca²⁺ with PO₄³⁻; charge balance builds Ca₃(PO₄)₂. The other product of every neutralization is water.

H₃PO₄ + Ca(OH)₂ → Ca₃(PO₄)₂ + H₂O (skeleton)
Ca₃(PO₄)₂: 3(2+) + 2(3−) = 0 ✓
Dr. Karmach

Worked example 2: the products

H₃PO₄(aq) + Ca(OH)₂(aq) → ?
wanted: the products and the coefficients

Predict the products

The salt pairs Ca²⁺ with PO₄³⁻; charge balance builds Ca₃(PO₄)₂. The other product of every neutralization is water.

H₃PO₄ + Ca(OH)₂ → Ca₃(PO₄)₂ + H₂O (skeleton)
Ca₃(PO₄)₂: 3(2+) + 2(3−) = 0 ✓
The salt's formula comes from the ion charges, never from the coefficients: the products must be neutral before any balancing starts.
Dr. Karmach

Worked example 2: the coefficients

H₃PO₄ + Ca(OH)₂ → Ca₃(PO₄)₂ + H₂O (skeleton)
products predicted · wanted: the coefficients

Match H⁺ to OH⁻

Balancing a neutralization needs equal moles of H⁺ and OH⁻: one water forms per pair. Three H⁺ against two OH⁻ meet at six: write 2 H₃PO₄ and 3 Ca(OH)₂.

2 H₃PO₄ + 3 Ca(OH)₂ → Ca₃(PO₄)₂ + 6 H₂O
H⁺: 2 × 3 = 6 · OH⁻: 3 × 2 = 6 · 6 pairs → 6 H₂O
Dr. Karmach

Worked example 2: the coefficients

H₃PO₄ + Ca(OH)₂ → Ca₃(PO₄)₂ + H₂O (skeleton)
products predicted · wanted: the coefficients
Match H⁺ to OH⁻
2 H₃PO₄ + 3 Ca(OH)₂ → Ca₃(PO₄)₂ + 6 H₂O
H⁺: 2 × 3 = 6 · OH⁻: 3 × 2 = 6 · 6 pairs → 6 H₂O
Recheck every count
2 H₃PO₄(aq) + 3 Ca(OH)₂(aq) → Ca₃(PO₄)₂(s) + 6 H₂O(l)
Ca: 3 = 3 ✓ · P: 2 = 2 ✓ · H: 6 + 6 = 12 = 12 ✓ · O: 8 + 6 = 14 = 14 ✓
Dr. Karmach

Worked example 2: the coefficients

H₃PO₄ + Ca(OH)₂ → Ca₃(PO₄)₂ + H₂O (skeleton)
products predicted · wanted: the coefficients
Match H⁺ to OH⁻
2 H₃PO₄ + 3 Ca(OH)₂ → Ca₃(PO₄)₂ + 6 H₂O
H⁺: 2 × 3 = 6 · OH⁻: 3 × 2 = 6 · 6 pairs → 6 H₂O
Recheck every count
2 H₃PO₄(aq) + 3 Ca(OH)₂(aq) → Ca₃(PO₄)₂(s) + 6 H₂O(l)
Ca: 3 = 3 ✓ · P: 2 = 2 ✓ · H: 6 + 6 = 12 = 12 ✓ · O: 8 + 6 = 14 = 14 ✓
The coefficients 2 and 3 came from matching six H⁺ to six OH⁻, and one water forms per pair: 6 H₂O.
Dr. Karmach

Worked example 2: the route on the chart

2 H₃PO₄(aq) + 3 Ca(OH)₂(aq) → Ca₃(PO₄)₂(s) + 6 H₂O(l)
partner: a hydroxide · exchange: salt + water · nothing breaks up

A hydroxide partner stops after the exchange: a salt and water, no gas. ✓
Dr. Karmach

Practice 3: an acid and a hydroxide

hydroiodic acid + barium hydroxide → ?
both solutions clear · wanted: the balanced equation, with states

Hydroiodic acid is mixed with a solution of barium hydroxide. Which equation shows the reaction?

  1. HI(aq) + Ba(OH)₂(aq) → BaI₂(aq) + H₂O(l)
  2. HI(aq) + BaOH(aq) → BaI(aq) + H₂O(l)
  3. 2 HI(aq) + Ba(OH)₂(aq) → BaI₂(s) + 2 H₂O(l)
  4. 2 HI(aq) + Ba(OH)₂(aq) → BaI₂(aq) + 2 H₂O(l)
Dr. Karmach

Practice 3: answer D

2 HI(aq) + Ba(OH)₂(aq) → BaI₂(aq) + 2 H₂O(l) (answer D)
H⁺: 2 × 1 = 2 · OH⁻: 1 × 2 = 2 · Ba: 1 = 1 · I: 2 = 2 · H: 2 + 2 = 4 = 4 · O: 2 = 2 ✓

A skipped matching H⁺ to OH⁻: I: 1 ≠ 2, and H: 1 + 2 = 3 ≠ 2. B wrote barium hydroxide as BaOH: (2+) + (1−) = 1+, and Ba²⁺ needs two OH⁻. C called BaI₂ insoluble; iodides dissolve except with Ag⁺, Pb²⁺, Hg₂²⁺.

Two H⁺ meet two OH⁻: two waters, and the salt stays dissolved. ✓
Dr. Karmach

Practice 3: the route on the chart

2 HI(aq) + Ba(OH)₂(aq) → BaI₂(aq) + 2 H₂O(l) (answer D)
partner: a hydroxide · exchange: salt + water · nothing breaks up

The same lane as the phosphoric acid example: a hydroxide partner ends at salt plus water. ✓
Dr. Karmach

Worked example 3: acid plus a carbonate

Na₂CO₃(aq) + 2 HCl(aq) → ?
wanted: the products, found in two steps

Washing soda meets hydrochloric acid, and the mixture fizzes. The gas is the product to explain. Work the exchange first, then watch what the exchange product does.

Dr. Karmach

Worked example 3: the exchange

Na₂CO₃(aq) + 2 HCl(aq) → ?
the mixture fizzes: a gas leaves

First reaction · exchange partners

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
Na: 2 = 2 · C: 1 = 1 · O: 3 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
Dr. Karmach

Worked example 3: the exchange

Na₂CO₃(aq) + 2 HCl(aq) → ?
the mixture fizzes: a gas leaves

First reaction · exchange partners

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
Na: 2 = 2 · C: 1 = 1 · O: 3 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
The exchange is ordinary. The product H₂CO₃, carbonic acid, is not: it cannot survive in water.
Dr. Karmach

Worked example 3: the exchange

Na₂CO₃(aq) + 2 HCl(aq) → ?
the mixture fizzes: a gas leaves

First reaction · exchange partners

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
Na: 2 = 2 · C: 1 = 1 · O: 3 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
The exchange is ordinary. The product H₂CO₃, carbonic acid, is not: it cannot survive in water.
On paper the swap looks routine. The fizz says otherwise: one of these products refuses to stay in the water.
Dr. Karmach

Worked example 3: the gas appears

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
the exchange product H₂CO₃ cannot survive in water

Second reaction · the unstable product breaks up

H₂CO₃(aq) → H₂O(l) + CO₂(g)
H: 2 = 2 · C: 1 = 1 · O: 3 = 1 + 2 = 3 ✓ · the fizz is CO₂ leaving
Dr. Karmach

Worked example 3: the gas appears

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
the exchange product H₂CO₃ cannot survive in water
Second reaction · the unstable product breaks up
H₂CO₃(aq) → H₂O(l) + CO₂(g)
H: 2 = 2 · C: 1 = 1 · O: 3 = 1 + 2 = 3 ✓ · the fizz is CO₂ leaving
Overall
Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂O(l) + CO₂(g)
Na: 2 = 2 · C: 1 = 1 · O: 3 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
Dr. Karmach

Worked example 3: the gas appears

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂CO₃(aq)
the exchange product H₂CO₃ cannot survive in water
Second reaction · the unstable product breaks up
H₂CO₃(aq) → H₂O(l) + CO₂(g)
H: 2 = 2 · C: 1 = 1 · O: 3 = 1 + 2 = 3 ✓ · the fizz is CO₂ leaving
Overall
Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂O(l) + CO₂(g)
Na: 2 = 2 · C: 1 = 1 · O: 3 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
Acid plus a carbonate or bicarbonate always ends here: CO₂, water, and a salt. The two-step explains the fizz that one overall line hides.
Dr. Karmach

Worked example 3: the route on the chart

Na₂CO₃(aq) + 2 HCl(aq) → 2 NaCl(aq) + H₂O(l) + CO₂(g)
partner: a carbonate · exchange: NaCl + H₂CO₃ · H₂CO₃ breaks up

A carbonate partner runs the full lane: the exchange, then the breakup into water and CO₂. ✓
Dr. Karmach

Three products that never survive

H₂CO₃ → H₂O(l) + CO₂(g) · H₂SO₃ → H₂O(l) + SO₂(g) · NH₄OH → H₂O(l) + NH₃(g)
memorize all three · each breaks into water plus a gas the moment it forms

Three exchange products are unstable. When one appears among the products, replace it with its water and gas. Acid plus a carbonate or bicarbonate always gives CO₂, water, and a salt.

Dr. Karmach

Your turn: acid plus a sulfite

K₂SO₃(aq) + 2 HCl(aq) → ?
exchange first · then check the unstable-products list
step your work
exchange partners 2 KCl +
unstable product breaks up H₂SO₃ → H₂O(l) +
overall equation K₂SO₃(aq) + 2 HCl(aq) → 2 KCl(aq) + +

Complete all three lines.

Dr. Karmach

Your turn: acid plus a sulfite

K₂SO₃(aq) + 2 HCl(aq) → ?
exchange first · then check the unstable-products list
step your work
exchange partners 2 KCl +
unstable product breaks up H₂SO₃ → H₂O(l) +
overall equation K₂SO₃(aq) + 2 HCl(aq) → 2 KCl(aq) + +

Complete all three lines.

K₂SO₃(aq) + 2 HCl(aq) → 2 KCl(aq) + H₂O(l) + SO₂(g)
K: 2 = 2 · S: 1 = 1 · O: 3 = 1 + 2 = 3 · H: 2 = 2 · Cl: 2 = 2 ✓
An acid meeting a sulfite releases SO₂, the sharp smell of a struck match.
Dr. Karmach

Practice 4

NaHCO₃(aq) + CH₃COOH(aq) → ?
baking soda + vinegar's acetic acid

Baking soda is stirred into vinegar. Which products form?

  1. NaCH₃COO(aq) + H₂CO₃(aq)
  2. NaCH₃COO(aq) + H₂(g)
  3. No reaction: acetic acid is weak, so its molecules stay whole
  4. NaCH₃COO(aq) + H₂O(l) + CO₂(g)
Dr. Karmach

Practice 4: answer D

NaHCO₃(aq) + CH₃COOH(aq) → NaCH₃COO(aq) + H₂CO₃(aq)
first reaction: exchange partners · H₂CO₃ is on the never-survive list
NaHCO₃(aq) + CH₃COOH(aq) → NaCH₃COO(aq) + H₂O(l) + CO₂(g) (answer D)
Na: 1 = 1 · C: 1 + 2 = 3 = 2 + 1 · H: 1 + 4 = 5 = 3 + 2 · O: 3 + 2 = 5 = 2 + 1 + 2 ✓

A stopped at the exchange: H₂CO₃ breaks into H₂O and CO₂ the moment it forms. B expects H₂, the gas an acid releases from an active metal; a bicarbonate trades partners instead. C reads weak as unreactive: weak describes the fraction ionized, and acid plus a carbonate or bicarbonate always gives CO₂, water, and a salt.

The fizz in the cup is the CO₂ from the H₂CO₃ breakup, even with a weak acid.
Dr. Karmach

Practice 4: the route on the chart

NaHCO₃(aq) + CH₃COOH(aq) → NaCH₃COO(aq) + H₂O(l) + CO₂(g) (answer D)
partner: a bicarbonate · exchange: NaCH₃COO + H₂CO₃ · H₂CO₃ breaks up

A weak acid takes the same lane as HCl. The partner picks the lane; the acid's strength does not. ✓
Dr. Karmach

Practice 5: bicarbonate and sulfuric acid

potassium bicarbonate + sulfuric acid → ?
both solutions clear · wanted: the balanced overall equation, with states

Potassium bicarbonate solution is poured into sulfuric acid. Which equation shows the overall reaction?

  1. 2 KHCO₃(aq) + H₂SO₄(aq) → K₂SO₄(aq) + 2 H₂CO₃(aq)
  2. 2 KHCO₃(aq) + H₂SO₄(aq) → K₂SO₄(aq) + 2 H₂O(l) + 2 CO₂(g)
  3. KHCO₃(aq) + H₂SO₄(aq) → KSO₄(aq) + H₂O(l) + CO₂(g)
  4. 2 KHCO₃(aq) + H₂SO₄(aq) → K₂SO₄(aq) + H₂O(l) + CO₂(g)
  5. No reaction: K₂SO₄ is soluble, so nothing leaves the solution
Dr. Karmach

Practice 5: answer B

2 KHCO₃(aq) + H₂SO₄(aq) → K₂SO₄(aq) + 2 H₂CO₃(aq)
first reaction: exchange partners · the two H⁺ of H₂SO₄ go to two HCO₃⁻ · H₂CO₃ never survives
2 KHCO₃(aq) + H₂SO₄(aq) → K₂SO₄(aq) + 2 H₂O(l) + 2 CO₂(g) (answer B)
K: 2 = 2 · H: 2 + 2 = 4 = 4 · C: 2 = 2 · S: 1 = 1 · O: 2 × 3 + 4 = 10 = 4 + 2 + 4 ✓

A stopped at the exchange. C swapped partners one for one: KSO₄ strands a charge, (1+) + (2−) = 1−. D dropped the 2 in the breakup: C: 2 ≠ 1, O: 10 ≠ 4 + 1 + 2 = 7. E looked only for a precipitate; a gas leaving also drives the reaction.

Each bicarbonate makes one H₂CO₃, and each H₂CO₃ makes one CO₂: the 2 carries through to the gas. ✓
Dr. Karmach

Practice 5: the route on the chart

2 KHCO₃(aq) + H₂SO₄(aq) → K₂SO₄(aq) + 2 H₂O(l) + 2 CO₂(g) (answer B)
partner: a bicarbonate · exchange: K₂SO₄ + 2 H₂CO₃ · each H₂CO₃ breaks up

A diprotic acid runs the same lane twice per formula unit: two H₂CO₃, two CO₂. ✓
Dr. Karmach

2 · Acids and Bases, Definitions and Neutralization

Recognize an acid or a base from its properties, state the Arrhenius and Brønsted–Lowry definitions, identify the proton donor and acceptor in an equation, and predict the salt and water a neutralization forms.

Dr. Karmach

Sour, bitter, slippery

Lemon juice and vinegar taste sour. Soap and baking soda taste bitter and feel slippery. A strip of litmus paper sorts household chemicals into the same two families.

Dr. Karmach

What acid reactions share

HBr + KOH → KBr + H₂O · 2 HCl + K₂CO₃ → 2 KCl + H₂O + CO₂
review · acid + hydroxide: salt + water · acid + carbonate: salt + water + CO₂, from H₂CO₃ → H₂O + CO₂ · H: 1 + 1 = 2 ✓ · H: 2 = 2 ✓

In each, the acid's H leaves as H⁺ and lands on a partner. OH⁻ becomes H₂O. CO₃²⁻ becomes H₂CO₃.

Which reactant lost its H in the first reaction?

Dr. Karmach

What acid reactions share

HBr + KOH → KBr + H₂O · 2 HCl + K₂CO₃ → 2 KCl + H₂O + CO₂
review · acid + hydroxide: salt + water · acid + carbonate: salt + water + CO₂, from H₂CO₃ → H₂O + CO₂ · H: 1 + 1 = 2 ✓ · H: 2 = 2 ✓

In each, the acid's H leaves as H⁺ and lands on a partner. OH⁻ becomes H₂O. CO₃²⁻ becomes H₂CO₃.

Which reactant lost its H in the first reaction?

HBr. Its H now sits in H₂O. ✓
Dr. Karmach

Two families of compounds

Acids share one property set; bases share another. One cause: every member of a family makes the same ion in water.

acids: taste sour · turn litmus red · react with active metals, releasing H₂ gas
bases: taste bitter · feel slippery · turn litmus blue
both families: dissolved, they conduct electricity

Taste and touch are never tests in a laboratory. Litmus does that work safely.

Dr. Karmach

Arrhenius: the ion each family makes

Dissolved in water, an Arrhenius acid produces H⁺, which rides on a water molecule as the hydronium ion H₃O⁺. An Arrhenius base produces OH⁻, the hydroxide ion.

HCl → H⁺ + Cl⁻, the H⁺ carried as H₃O⁺ · NaOH → Na⁺ + OH⁻
free ions carry current: this is why both families conduct as electrolytes
Dr. Karmach

Why H⁺ is called a proton

H atom: 1 proton + 1 electron · H⁺ ion: 1 proton, 0 electrons
an H⁺ ion is a bare proton · donating a proton = giving away H⁺

Moving one H⁺ changes two things together: one H in the formula and one unit of charge. Apply it to water.

Dr. Karmach

Why H⁺ is called a proton

H atom: 1 proton + 1 electron · H⁺ ion: 1 proton, 0 electrons
an H⁺ ion is a bare proton · donating a proton = giving away H⁺

Moving one H⁺ changes two things together: one H in the formula and one unit of charge. Apply it to water.

H₂O − H⁺ → OH⁻ · H₂O + H⁺ → H₃O⁺
H: 2 − 1 = 1, charge 0 − 1 = 1− · H: 2 + 1 = 3, charge 0 + 1 = 1+
Dr. Karmach

Brønsted–Lowry: donor and acceptor

A wider definition tracks the H⁺ itself. A Brønsted–Lowry acid donates a proton; a base accepts one. Every Arrhenius acid or base still qualifies, and the label now depends on the reaction.

HCl + H₂O → H₃O⁺ + Cl⁻
HCl loses the H⁺: donor, the acid · H₂O gains it: acceptor, the base
Dr. Karmach

Conjugate pairs

NH₃ holds no OH⁻, yet it accepts H⁺ from water: a base. The ⇌ transfer also runs backward. Species differing by one H⁺ form a conjugate acid-base pair.

Dr. Karmach

Your turn: write the conjugate

conjugate base = the acid minus one H⁺: charge drops by 1
conjugate acid = the base plus one H⁺: charge rises by 1
given wanted answer
HSO₄⁻ conjugate base
H₂PO₄⁻ conjugate base
HCO₃⁻ conjugate acid
OH⁻ conjugate acid

Change one H and the charge by one, together.

Dr. Karmach

Your turn: write the conjugate

conjugate base = the acid minus one H⁺: charge drops by 1
conjugate acid = the base plus one H⁺: charge rises by 1
given wanted answer
HSO₄⁻ conjugate base
H₂PO₄⁻ conjugate base
HCO₃⁻ conjugate acid
OH⁻ conjugate acid

Change one H and the charge by one, together.

HSO₄⁻ → SO₄²⁻ · H₂PO₄⁻ → HPO₄²⁻ · HCO₃⁻ → H₂CO₃ · OH⁻ → H₂O
each H removed takes a 1+ with it: 1− becomes 2− · each H added brings a 1+: 1− becomes 0
Dr. Karmach

The method

  1. Track the proton. Which species lost an H⁺? Which gained?
  2. Label donor and acceptor. Donor = acid, acceptor = base.
  3. Predict the products. Base's cation + acid's anion = the salt; H⁺ + OH⁻ = water.
  4. Balance and check.

Dr. Karmach

Guided example: green apples

H₂C₄H₄O₅(aq) + H₂O(l) ⇌ H₃O⁺(aq) + HC₄H₄O₅⁻(aq)
H: 6 + 2 = 3 + 5 ✓ · wanted: the acid, the base, the conjugate acid, the conjugate base

Malic acid, H₂C₄H₄O₅, gives green apples their tartness. It hands one H⁺ to water. Label all four species.

Match each reactant to the product it becomes: same atoms, one H different.

Dr. Karmach

Guided example: solution

H₂C₄H₄O₅(aq) + H₂O(l) ⇌ H₃O⁺(aq) + HC₄H₄O₅⁻(aq)
wanted: acid, base, conjugate acid, conjugate base

Three moves: two method steps, then the partners.

Dr. Karmach

Guided example: solution

H₂C₄H₄O₅(aq) + H₂O(l) ⇌ H₃O⁺(aq) + HC₄H₄O₅⁻(aq)
wanted: acid, base, conjugate acid, conjugate base
Step 1 · Track the proton
H₂C₄H₄O₅ → HC₄H₄O₅⁻: one H fewer · H₂O → H₃O⁺: one H more
charge: 0 → 1− and 0 → 1+ · one H⁺ moved from H₂C₄H₄O₅ to H₂O
Dr. Karmach

Guided example: solution

H₂C₄H₄O₅(aq) + H₂O(l) ⇌ H₃O⁺(aq) + HC₄H₄O₅⁻(aq)
wanted: acid, base, conjugate acid, conjugate base
Step 1 · Track the proton
H₂C₄H₄O₅ → HC₄H₄O₅⁻: one H fewer · H₂O → H₃O⁺: one H more
charge: 0 → 1− and 0 → 1+ · one H⁺ moved from H₂C₄H₄O₅ to H₂O
Step 2 · Label donor and acceptor

H₂C₄H₄O₅ lost the H⁺: the donor, the acid. H₂O gained it: the acceptor, the base.

Dr. Karmach

Guided example: solution

H₂C₄H₄O₅(aq) + H₂O(l) ⇌ H₃O⁺(aq) + HC₄H₄O₅⁻(aq)
wanted: acid, base, conjugate acid, conjugate base
Step 1 · Track the proton
H₂C₄H₄O₅ → HC₄H₄O₅⁻: one H fewer · H₂O → H₃O⁺: one H more
charge: 0 → 1− and 0 → 1+ · one H⁺ moved from H₂C₄H₄O₅ to H₂O
Step 2 · Label donor and acceptor Name the conjugates
acid H₂C₄H₄O₅ → HC₄H₄O₅⁻, its conjugate base · base H₂O → H₃O⁺, its conjugate acid
pairs: H₂C₄H₄O₅/HC₄H₄O₅⁻ and H₂O/H₃O⁺ · each pair differs by one H⁺ and one charge
Dr. Karmach

Guided example: solution

H₂C₄H₄O₅(aq) + H₂O(l) ⇌ H₃O⁺(aq) + HC₄H₄O₅⁻(aq)
wanted: acid, base, conjugate acid, conjugate base
Step 1 · Track the proton
H₂C₄H₄O₅ → HC₄H₄O₅⁻: one H fewer · H₂O → H₃O⁺: one H more
charge: 0 → 1− and 0 → 1+ · one H⁺ moved from H₂C₄H₄O₅ to H₂O
Step 2 · Label donor and acceptor Name the conjugates
acid H₂C₄H₄O₅ → HC₄H₄O₅⁻, its conjugate base · base H₂O → H₃O⁺, its conjugate acid
pairs: H₂C₄H₄O₅/HC₄H₄O₅⁻ and H₂O/H₃O⁺ · each pair differs by one H⁺ and one charge
Read backward, HC₄H₄O₅⁻ takes an H⁺: a base. H₃O⁺ gives one up: an acid. The conjugate labels fit. ✓
Dr. Karmach

Guided example: the route on the map

H₂C₄H₄O₅ + H₂O ⇌ H₃O⁺ + HC₄H₄O₅⁻
found: acid H₂C₄H₄O₅ · base H₂O · conjugate acid H₃O⁺ · conjugate base HC₄H₄O₅⁻

The top lane gave the labels. The dashed arrow carries them down: each label's partner sits across the ⇌. ✓
Dr. Karmach

Practice 1

What is the conjugate base of HPO₄²⁻?

  1. H₂PO₄⁻
  2. PO₄³⁻
  3. PO₄²⁻
  4. HPO₄³⁻
Dr. Karmach

Practice 1: answer B

HPO₄²⁻ − H⁺ → PO₄³⁻ (answer B)
H: 1 − 1 = 0 · charge: 2− minus one 1+ = 3−

A added an H⁺ instead of removing one: H₂PO₄⁻ is the conjugate acid. C removed the H but kept the 2− charge; the H⁺ takes its 1+ with it. D lowered the charge but left the H in place.

A conjugate base has one H fewer and one more negative charge than its acid. ✓
Dr. Karmach

Practice 1: the route on the map

HPO₄²⁻ − H⁺ → PO₄³⁻
given: one formula, no reaction · found: the conjugate base PO₄³⁻

A formula given alone needs no labeling first: the conjugate lane applies directly. ✓
Dr. Karmach

Worked example 1: nitric acid in water

HNO₃(aq) + H₂O(l) → H₃O⁺(aq) + NO₃⁻(aq)
one proton changes hands · H: 1 + 2 = 3 on each side ✓

Nitric acid ionizes in water. Identify the Brønsted–Lowry acid and the Brønsted–Lowry base.

Dr. Karmach

Worked example 1: solution

Step 1 · Track the proton

HNO₃ → NO₃⁻, one H⁺ lighter · H₂O → H₃O⁺, one H⁺ heavier
H check: 1 + 2 = 3 before and after ✓
Dr. Karmach

Worked example 1: solution

Step 1 · Track the proton

HNO₃ → NO₃⁻, one H⁺ lighter · H₂O → H₃O⁺, one H⁺ heavier
H check: 1 + 2 = 3 before and after ✓
Step 2 · Label donor and acceptor

HNO₃ lost the proton: the donor, the Brønsted–Lowry acid. H₂O gained it: the acceptor, the base.

Dr. Karmach

Worked example 1: solution

Step 1 · Track the proton

HNO₃ → NO₃⁻, one H⁺ lighter · H₂O → H₃O⁺, one H⁺ heavier
H check: 1 + 2 = 3 before and after ✓
Step 2 · Label donor and acceptor
The acid ends one H smaller; the base ends one H larger. The products record the transfer: H₃O⁺ carries the proton, NO₃⁻ is the donor's leftover.
Dr. Karmach

Worked example 1: the route on the map

HNO₃(aq) + H₂O(l) → H₃O⁺(aq) + NO₃⁻(aq)
found: HNO₃ the acid (donor) · H₂O the base (acceptor)

Only the acid and the base were wanted: the top lane alone. ✓
Dr. Karmach

Worked example 2: ammonia in water

NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
no OH⁻ anywhere inside NH₃ · H: 3 + 2 = 5 on each side ✓

Ammonia contains no hydroxide, yet its solution turns litmus blue. Identify the donor and the acceptor.

Dr. Karmach

Worked example 2: solution

Step 1 · Track the proton

NH₃ → NH₄⁺, one H⁺ heavier · H₂O → OH⁻, one H⁺ lighter
H check: 3 + 2 = 5 before and after ✓
Dr. Karmach

Worked example 2: solution

Step 1 · Track the proton

NH₃ → NH₄⁺, one H⁺ heavier · H₂O → OH⁻, one H⁺ lighter
H check: 3 + 2 = 5 before and after ✓
Step 2 · Label donor and acceptor

Water lost the proton: the donor, the acid in this reaction. NH₃ gained it: the acceptor, the base. Arrhenius has no name for NH₃ here; Brønsted–Lowry does.

Dr. Karmach

Worked example 2: solution

Step 1 · Track the proton

NH₃ → NH₄⁺, one H⁺ heavier · H₂O → OH⁻, one H⁺ lighter
H check: 3 + 2 = 5 before and after ✓
Step 2 · Label donor and acceptor
The OH⁻ that turns litmus blue appears because water gave up a proton. A base needs no OH⁻ of its own.
Dr. Karmach

Worked example 2: the route on the map

NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
found: H₂O the acid (donor) · NH₃ the base (acceptor)

The same top lane. Here water lands on the acid side: the label depends on the reaction. ✓
Dr. Karmach

Practice 2

SO₃²⁻(aq) + H₂O(l) ⇌ HSO₃⁻(aq) + OH⁻(aq)
H: 0 + 2 = 1 + 1 ✓

Which two species form a conjugate acid-base pair?

  1. SO₃²⁻ and HSO₃⁻
  2. SO₃²⁻ and H₂O
  3. HSO₃⁻ and OH⁻
  4. H₂O and HSO₃⁻
Dr. Karmach

Practice 2: answer A

SO₃²⁻ → HSO₃⁻: one H⁺ gained · H₂O → OH⁻: one H⁺ lost
pairs: SO₃²⁻/HSO₃⁻ (answer A) and H₂O/OH⁻ · charge: 2− → 1− and 0 → 1−

B paired the two reactants: the acid and the base react with each other, and neither becomes the other. C paired the two products. D paired the two species that hold the H⁺, the acid before and the conjugate acid after: two different species.

A conjugate pair is one species before the transfer and the same species after: one H⁺ apart, one on each side. ✓
Dr. Karmach

Practice 2: the route on the map

SO₃²⁻ + H₂O ⇌ HSO₃⁻ + OH⁻
found: base SO₃²⁻ · acid H₂O · pairs SO₃²⁻/HSO₃⁻ and H₂O/OH⁻

Labels first, then each partner across the ⇌. The second pair, H₂O/OH⁻, was not among the choices. ✓
Dr. Karmach

Neutralization: acid + base

acid + base → salt + water
H⁺ + OH⁻ join as H₂O · the salt = the base's cation + the acid's anion

Mix the two families and both property sets vanish. In chemistry a salt is any cation-anion compound left behind, not only table salt: KBr, CaCl₂, and K₂SO₄ all qualify.

Dr. Karmach

Worked example 3: predict the products

HCl(aq) + NaOH(aq) → ?
given: the acid HCl and the base NaOH · wanted: the products, balanced

Hydrochloric acid meets sodium hydroxide. Predict both products and balance the equation.

Dr. Karmach

Worked example 3: solution

Step 1 · Track the proton

H⁺ + OH⁻ → H₂O
H: 1 + 1 = 2 ✓ · O: 1 = 1 ✓

The acid's H⁺ transfers to the OH⁻ the base provides.

Dr. Karmach

Worked example 3: solution

Step 1 · Track the proton

H⁺ + OH⁻ → H₂O
H: 1 + 1 = 2 ✓ · O: 1 = 1 ✓
Step 2 · Label donor and acceptor

HCl donates: the acid. The OH⁻ from NaOH accepts: the base.

Dr. Karmach

Worked example 3: solution

Step 1 · Track the proton

H⁺ + OH⁻ → H₂O
H: 1 + 1 = 2 ✓ · O: 1 = 1 ✓
Step 2 · Label donor and acceptor Step 3 · Predict the products
leftover ions: Na⁺ from the base · Cl⁻ from the acid
1+ and 1− pair one to one: the salt is NaCl
Dr. Karmach

Worked example 3: solution

Step 1 · Track the proton

H⁺ + OH⁻ → H₂O
H: 1 + 1 = 2 ✓ · O: 1 = 1 ✓
Step 2 · Label donor and acceptor Step 3 · Predict the products
leftover ions: Na⁺ from the base · Cl⁻ from the acid
1+ and 1− pair one to one: the salt is NaCl
Step 4 · Balance and check
HCl + NaOH → NaCl + H₂O
H: 1 + 1 = 2 ✓ · Cl: 1 = 1 ✓ · Na: 1 = 1 ✓ · O: 1 = 1 ✓
Dr. Karmach

Worked example 3: solution

Step 1 · Track the proton

H⁺ + OH⁻ → H₂O
H: 1 + 1 = 2 ✓ · O: 1 = 1 ✓
Step 2 · Label donor and acceptor Step 3 · Predict the products
leftover ions: Na⁺ from the base · Cl⁻ from the acid
1+ and 1− pair one to one: the salt is NaCl
Step 4 · Balance and check
HCl + NaOH → NaCl + H₂O
H: 1 + 1 = 2 ✓ · Cl: 1 = 1 ✓ · Na: 1 = 1 ✓ · O: 1 = 1 ✓
Sour gone, slippery gone: a neutral salt and water remain.
Dr. Karmach

Worked example 3: the route on the map

HCl + NaOH → NaCl + H₂O
found: H⁺ + OH⁻ → H₂O · salt NaCl from Na⁺ and Cl⁻

Products were wanted, so the bottom lane: water from H⁺ + OH⁻, the salt from the leftover ions. ✓
Dr. Karmach

Your turn: sulfuric acid and potassium hydroxide

H₂SO₄(aq) + KOH(aq) → ?
SO₄²⁻ carries 2− · K⁺ carries 1+ · H₂SO₄ can donate 2 H⁺
step question answer
1 · Track the proton how many H⁺ does the acid donate?
2 · Label donor and acceptor which species donates?
3 · Predict the products the salt from K⁺ and SO₄²⁻? + water
4 · Balance and check coefficients on KOH and H₂O?

Complete the four steps.

Dr. Karmach

Your turn: sulfuric acid and potassium hydroxide

H₂SO₄(aq) + KOH(aq) → ?
SO₄²⁻ carries 2− · K⁺ carries 1+ · H₂SO₄ can donate 2 H⁺
step question answer
1 · Track the proton how many H⁺ does the acid donate?
2 · Label donor and acceptor which species donates?
3 · Predict the products the salt from K⁺ and SO₄²⁻? + water
4 · Balance and check coefficients on KOH and H₂O?

Complete the four steps.

H₂SO₄ + 2 KOH → K₂SO₄ + 2 H₂O
two H⁺ donated, so two OH⁻ needed · H: 2 + 2 = 4 ✓ · O: 4 + 2 = 6 ✓ · K: 2 = 2 ✓ · S: 1 = 1 ✓
Dr. Karmach

Where this goes wrong

"A base must contain OH." NH₃ + H₂O ⇌ NH₄⁺ + OH⁻: ammonia accepts a proton, and the OH⁻ appears from water. Proton acceptor is the wider definition, and it covers NH₃.
"Salt means table salt." A salt is any cation-anion compound a neutralization leaves behind: KBr, MgCl₂, and K₂SO₄ are all salts. NaCl is one example, not the definition.
Pairing salt ions without checking charge. K⁺ with SO₄²⁻ written KSO₄ totals 1 − 2 = −1, not neutral. Two K⁺ cancel the 2−: K₂SO₄, with 2(1+) + (2−) = 0.
Counting H⁺ and H₃O⁺ as different ions. Same species: the proton rides on a water molecule. HCl in water makes two ions, H₃O⁺ and Cl⁻, never three.
Dr. Karmach

Practice 3

HNO₃(aq) + Ca(OH)₂(aq) → ?
NO₃⁻ carries 1− · Ca²⁺ carries 2+

Nitric acid neutralizes calcium hydroxide. Which products form?

  1. CaNO₃ and H₂O
  2. Ca(NO₃)₂ and H₂
  3. Ca(NO₃)₂ and H₂O
  4. Ca(NO₂)₂ and H₂O
Dr. Karmach

Practice 3: answer C

2 HNO₃ + Ca(OH)₂ → Ca(NO₃)₂ + 2 H₂O (answer C)
Ca: 1 = 1 ✓ · N: 2 = 2 ✓ · H: 2 + 2 = 4 ✓ · O: 6 + 2 = 8 = 6 + 2 ✓

A pairs Ca²⁺ with a single NO₃⁻: the charge total 2 − 1 = +1 is not zero, so two nitrates are needed, in parentheses. B makes H₂ gas: that is the acid + active metal reaction; here H⁺ meets OH⁻ and leaves as water. D swaps in nitrite, NO₂⁻: the acid supplied nitrate, NO₃⁻.

The salt keeps the ions that did not become water, paired until the total charge is zero.
Dr. Karmach

Practice 3: the route on the map

2 HNO₃ + Ca(OH)₂ → Ca(NO₃)₂ + 2 H₂O
found: 2 H⁺ + 2 OH⁻ → 2 H₂O · salt Ca(NO₃)₂: (2+) + 2(1−) = 0

The bottom lane again. The check box caught the charge: one Ca²⁺ needs two NO₃⁻. ✓
Dr. Karmach

Practice 4

HCO₃⁻(aq) + OH⁻(aq) → CO₃²⁻(aq) + H₂O(l)
H: 1 + 1 = 0 + 2 ✓

Which species is the conjugate base in this reaction?

  1. HCO₃⁻
  2. OH⁻
  3. H₂O
  4. CO₃²⁻
Dr. Karmach

Practice 4: answer D

HCO₃⁻ → CO₃²⁻: one H⁺ lost · OH⁻ → H₂O: one H⁺ gained
acid HCO₃⁻ · base OH⁻ · conjugate base CO₃²⁻ (answer D) · conjugate acid H₂O

A named the acid itself; its conjugate base is what it becomes. B named the base, a reactant. C swapped the roles, reading HCO₃⁻ as the base; here OH⁻ pulls the H⁺ off HCO₃⁻, so H₂O is the conjugate acid.

HCO₃⁻ gives up an H⁺ here. Toward an acid it takes one and becomes H₂CO₃: one species, either role. ✓
Dr. Karmach

Practice 4: the route on the map

HCO₃⁻ + OH⁻ → CO₃²⁻ + H₂O
found: acid HCO₃⁻ · base OH⁻ · conjugate base CO₃²⁻ · conjugate acid H₂O

Both reactants carry H. The top lane decides which one lost it; the conjugate lane follows. ✓
Dr. Karmach

Practice 5

HCN + NH₃ ⇌ NH₄⁺ + CN⁻
H: 1 + 3 = 4 on each side ✓

Read the reaction right to left. In the reverse direction, which species acts as the Brønsted–Lowry acid?

  1. HCN
  2. CN⁻
  3. NH₃
  4. NH₄⁺
Dr. Karmach

Practice 5: answer D

reverse: NH₄⁺ + CN⁻ → NH₃ + HCN
NH₄⁺ → NH₃, one H⁺ lighter: the donor, the acid (answer D) · CN⁻ → HCN, one H⁺ heavier: the base

A kept the forward roles: HCN donates left to right, but read right to left it is a product, rebuilt when CN⁻ takes a proton. B swapped donor and acceptor: CN⁻ gains the H⁺, which makes it the reverse base. C is the forward base; in reverse NH₃ is a product, left behind when NH₄⁺ gives up its proton.

Each conjugate pair trades roles across the ⇌: HCN/CN⁻ and NH₄⁺/NH₃. The reverse acid is the forward base's conjugate, NH₄⁺.
Dr. Karmach

Practice 5: the route on the map

HCN + NH₃ ⇌ NH₄⁺ + CN⁻
forward: acid HCN · base NH₃ · conjugate acid NH₄⁺ · conjugate base CN⁻

Forward labels first, then their partners. Read right to left, the conjugate acid NH₄⁺ does the donating. ✓
Dr. Karmach

3 · The pH Scale

Place any solution on the pH ladder (acidic below 7, neutral 7 at 25 °C, basic above 7), read a whole-number pH straight from [H₃O⁺] written as a power of ten and run the read in reverse, and compare two solutions by factors of ten.

Dr. Karmach

The number on the bottle

Shampoo labels, pool test strips, and soil kits all report pH. One number places lemon juice, black coffee, baking soda, and bleach on the same 0 to 14 ladder.

Dr. Karmach

Every water solution holds both ions

Water itself makes both: a few molecules trade a proton. Both H₃O⁺ and OH⁻ are present in every water solution, and they see-saw: more of one always means less of the other.

2 H₂O ⇌ H₃O⁺ + OH⁻
acidic = H₃O⁺ ahead · basic = OH⁻ ahead · neutral = an exact tie
Dr. Karmach

The ion product of water

Kw = [H₃O⁺][OH⁻] = 1.0 × 10⁻¹⁴ (at 25 °C)
pure water: [H₃O⁺] = [OH⁻] = 1.0 × 10⁻⁷ M · (1.0 × 10⁻⁷)(1.0 × 10⁻⁷) = 1.0 × 10⁻¹⁴

The product of the two concentrations is fixed. Raise one and the other falls, so either concentration sets the other.

[H₃O⁺] = [OH⁻]: neutral · [H₃O⁺] > [OH⁻]: acidic · [H₃O⁺] < [OH⁻]: basic
at 25 °C: neutral at [H₃O⁺] = 1.0 × 10⁻⁷ M · acidic above it · basic below it
Dr. Karmach

The pH ladder: 0 to 14

pH places a solution on the see-saw: below 7 acidic (H₃O⁺ ahead), 7 neutral at 25 °C (a tie), above 7 basic (OH⁻ ahead).

Dr. Karmach

Each pH step is a factor of ten

The scale is compact because each step multiplies by ten. Two solutions one pH unit apart differ tenfold in H₃O⁺; three units apart, a thousandfold.

pH 2 vs pH 5: 3 steps apart
10 × 10 × 10 = 1000 × the H₃O⁺ · steps add, concentrations multiply
Dr. Karmach

Reading pH from [H₃O⁺]

Write [H₃O⁺] as 1 × 10⁻ⁿ M. The pH is n, the exponent's size. A smaller concentration carries a bigger n, so pH rises as acidity falls.

[H₃O⁺] = 1 × 10⁻⁵ M → pH 5 · [H₃O⁺] = 1 × 10⁻¹¹ M → pH 11
1 × 10⁻ⁿ M ↔ pH n · pure water at 25 °C: 1 × 10⁻⁷ M ↔ pH 7
Dr. Karmach

The method: pH from powers of ten

  1. Write [H₃O⁺] as 1 × 10⁻ⁿ M.
  2. Read the pH: pH = n.
  3. Place it: below 7 acidic, 7 neutral, above 7 basic.

Reversed, pH n means [H₃O⁺] = 1 × 10⁻ⁿ M.

Dr. Karmach

Worked example 1: black coffee

black coffee: [H₃O⁺] = 1 × 10⁻⁵ M
wanted: pH · acidic, neutral, or basic?

An analysis of black coffee reports the hydronium concentration directly. Find the pH and place the coffee on the ladder.

Dr. Karmach

Worked example 1: solution

Step 1 · Write [H₃O⁺] as 1 × 10⁻ⁿ M

[H₃O⁺] = 1 × 10⁻⁵ M
coefficient 1 · exponent −5 · n = 5
Dr. Karmach

Worked example 1: solution

Step 1 · Write [H₃O⁺] as 1 × 10⁻ⁿ M

[H₃O⁺] = 1 × 10⁻⁵ M
coefficient 1 · exponent −5 · n = 5
Step 2 · Read the pH: pH = n
[H₃O⁺] = 1 × 10⁻⁵ M → pH = 5
the pH is the exponent's size, sign dropped
Dr. Karmach

Worked example 1: solution

Step 1 · Write [H₃O⁺] as 1 × 10⁻ⁿ M

[H₃O⁺] = 1 × 10⁻⁵ M
coefficient 1 · exponent −5 · n = 5
Step 2 · Read the pH: pH = n
[H₃O⁺] = 1 × 10⁻⁵ M → pH = 5
the pH is the exponent's size, sign dropped
Step 3 · Place it: below 7 acidic, 7 neutral, above 7 basic
pH 5 → acidic
5 sits below 7 · H₃O⁺ ahead of OH⁻
Coffee sits 7 − 5 = 2 steps below neutral: 10 × 10 = 100 times the H₃O⁺ of pure water.
Dr. Karmach

Worked example 2: household ammonia

household ammonia cleaner: pH 11
wanted: [H₃O⁺] · acidic, neutral, or basic?

The label reports a pH, not a concentration. Run the read in reverse to recover [H₃O⁺].

Dr. Karmach

Worked example 2: solution

Reversed: pH n means [H₃O⁺] = 1 × 10⁻ⁿ M

The pH becomes the exponent, with a minus sign restored.

pH 11 → [H₃O⁺] = 1 × 10⁻¹¹ M
whole-number pH ↔ coefficient 1 · exponent = −11
Dr. Karmach

Worked example 2: solution

Reversed: pH n means [H₃O⁺] = 1 × 10⁻ⁿ M

pH 11 → [H₃O⁺] = 1 × 10⁻¹¹ M
whole-number pH ↔ coefficient 1 · exponent = −11
Place it: below 7 acidic, 7 neutral, above 7 basic
pH 11 → basic
11 sits above 7 · OH⁻ ahead, yet H₃O⁺ never reaches zero
A pH of 11 sits 11 − 7 = 4 steps above water's 7: far less H₃O⁺ than pure water, so the see-saw tips well toward OH⁻.
Dr. Karmach

With your calculator: pH = −log[H₃O⁺]

The log button reads the exponent for you. Enter the concentration, press log, flip the sign. Reversed, ten to the −pH rebuilds the concentration.

pH = −log[H₃O⁺] · −log(1 × 10⁻⁹) = 9
enter 1 EE 9 +/− · whole-power concentrations return whole-number pH
Dr. Karmach

The companion number: pOH

OH⁻ gets its own reading, pOH, on the same kind of 0 to 14 ladder. One line connects the two, so either number sets the other.

pH + pOH = 14 (at 25 °C)
pH 3 → pOH = 14 − 3 = 11 · low pH pairs with high pOH: the same see-saw
Dr. Karmach

The conversion chart

[H₃O⁺], [OH⁻], pH and pOH describe one solution; any one sets the other three. The top edge is the method; the bottom edge repeats it for OH⁻. Kw joins the concentrations, 14 the p-numbers.

Dr. Karmach

Guided example: seawater

seawater: [OH⁻] = 1 × 10⁻⁶ M
Kw = [H₃O⁺][OH⁻] = 1.0 × 10⁻¹⁴ · wanted: [H₃O⁺] and pH · acidic, neutral, or basic?

A seawater analysis reports the hydroxide concentration. Find [H₃O⁺] and the pH, then place the sample on the ladder.

Plan the route first: [OH⁻] sits in the bottom-left corner of the chart and pH in the top right. Kw crosses the left edge; −log runs along the top.

Dr. Karmach

Guided example: solution

seawater: [OH⁻] = 1 × 10⁻⁶ M
Kw = [H₃O⁺][OH⁻] = 1.0 × 10⁻¹⁴ · wanted: [H₃O⁺] and pH

Two moves reach the pH. A third places it.

Step 1 · Write [H₃O⁺] as 1 × 10⁻ⁿ M

Only [OH⁻] is given, so Kw supplies [H₃O⁺]. Dividing subtracts the exponents: −14 − (−6) = −8.

[H₃O⁺] = 1.0 × 10⁻¹⁴1 × 10⁻⁶ = 1 × 10⁻⁸ M
Dr. Karmach

Guided example: solution

seawater: [OH⁻] = 1 × 10⁻⁶ M
Kw = [H₃O⁺][OH⁻] = 1.0 × 10⁻¹⁴ · wanted: [H₃O⁺] and pH
Step 1 · Write [H₃O⁺] as 1 × 10⁻ⁿ M
[H₃O⁺] = 1.0 × 10⁻¹⁴1 × 10⁻⁶ = 1 × 10⁻⁸ M
Step 2 · Read the pH: pH = n
[H₃O⁺] = 1 × 10⁻⁸ M → pH = 8
n = 8 · the exponent's size, sign dropped
Dr. Karmach

Guided example: solution

seawater: [OH⁻] = 1 × 10⁻⁶ M
Kw = [H₃O⁺][OH⁻] = 1.0 × 10⁻¹⁴ · wanted: [H₃O⁺] and pH
Step 1 · Write [H₃O⁺] as 1 × 10⁻ⁿ M
[H₃O⁺] = 1.0 × 10⁻¹⁴1 × 10⁻⁶ = 1 × 10⁻⁸ M
Step 2 · Read the pH: pH = n
[H₃O⁺] = 1 × 10⁻⁸ M → pH = 8
n = 8 · the exponent's size, sign dropped
Step 3 · Place it: below 7 acidic, 7 neutral, above 7 basic
pH 8 sits above 7: basic. The pOH route agrees: pOH = 6, and 14 − 6 = 8. ✓
Dr. Karmach

Guided example: the route on the map

seawater: [OH⁻] = 1 × 10⁻⁶ M
given: [OH⁻] · found: [H₃O⁺] = 1 × 10⁻⁸ M · pH 8 · basic

Up the left edge with Kw, along the top with −log, then onto the ladder. ✓
Dr. Karmach

Worked example 3: tomato juice

tomato juice: [H₃O⁺] = 5.0 × 10⁻⁵ M
coefficient 5.0, not 1 · wanted: pH · acidic, neutral, or basic?

A coefficient other than 1 puts the pH between two whole numbers. Find it with the log key and report the right number of decimal places.

Dr. Karmach

Worked example 3: solution

tomato juice: [H₃O⁺] = 5.0 × 10⁻⁵ M
2 significant figures · wanted: pH

Bracket it between two powers of ten

5.0 × 10⁻⁵ M sits between 1 × 10⁻⁵ M (pH 5) and 1 × 10⁻⁴ M (pH 4), so the pH falls between 4 and 5.

Dr. Karmach

Worked example 3: solution

tomato juice: [H₃O⁺] = 5.0 × 10⁻⁵ M
2 significant figures · wanted: pH
Bracket it between two powers of ten pH = −log[H₃O⁺]
pH = −log(5.0 × 10⁻⁵) = 4.301
Dr. Karmach

Worked example 3: solution

tomato juice: [H₃O⁺] = 5.0 × 10⁻⁵ M
2 significant figures · wanted: pH
Bracket it between two powers of ten pH = −log[H₃O⁺]
pH = −log(5.0 × 10⁻⁵) = 4.301
Decimal places in the pH = significant figures in [H₃O⁺]
5.0 × 10⁻⁵ M → pH 4.30 → acidic
2 significant figures ↔ 2 decimal places · the 4 only marks the power of ten · below 7
4.30 falls between 4 and 5, as bracketed. Run it backward: 10−4.30 = 5.0 × 10⁻⁵ M, the starting concentration. ✓
Dr. Karmach

Worked example 3: the route on the map

tomato juice: [H₃O⁺] = 5.0 × 10⁻⁵ M
given: [H₃O⁺] · found: pH 4.30 · acidic

One edge, then the ladder. A coefficient other than 1 only adds decimals. ✓
Dr. Karmach

Your turn: vinegar

Vinegar measures [H₃O⁺] = 1 × 10⁻³ M. Fill each blank, then check.

step value
exponent n
pH
acidic, neutral, or basic
Dr. Karmach

Your turn: vinegar

Vinegar measures [H₃O⁺] = 1 × 10⁻³ M. Fill each blank, then check.

step value
exponent n
pH
acidic, neutral, or basic
[H₃O⁺] = 1 × 10⁻³ M → pH 3 → acidic
n = 3 · pH = n = 3 · 3 below 7 · pOH = 14 − 3 = 11
Dr. Karmach

Where this goes wrong

"pH 4 is twice as acidic as pH 8." The steps multiply. Four steps means 10 × 10 × 10 × 10 = 10,000 times the H₃O⁺, never 2 times.
Reading the ladder backward. pH climbs as H₃O⁺ falls. pH 2 holds more H₃O⁺ than pH 6, so the lower pH is the more acidic one.
"pH 0 means nothing is dissolved." pH 0 means [H₃O⁺] = 1 × 10⁰ M = 1 M: the crowded, strongly acidic end of the ladder.
"A basic solution has no H₃O⁺." Both ions live in every water solution. At pH 11 there is still 1 × 10⁻¹¹ M H₃O⁺; OH⁻ simply outnumbers it.
Dr. Karmach

Practice 1

A drain cleaner sample measures [H₃O⁺] = 1 × 10⁻¹² M. What is its pH?

  1. 12
  2. −12
  3. 2
  4. 7
Dr. Karmach

Practice 1 · answer: A

[H₃O⁺] = 1 × 10⁻¹² M → pH 12: basic (answer A)
1 × 10⁻ⁿ M ↔ pH n · 12 above 7 → basic

A: the exponent's size is the pH. B keeps the exponent's sign: pH = −log(10⁻¹²) = 12, positive. C is the pOH: 14 − 12 = 2. D assumes a tiny [H₃O⁺] means neutral; 10⁻¹² sits 12 − 7 = 5 steps below water's 10⁻⁷, which is 100,000 times less H₃O⁺ than neutral.

Less H₃O⁺ than pure water always lands above 7, never at it.
Dr. Karmach

Practice 1: the route on the map

drain cleaner: [H₃O⁺] = 1 × 10⁻¹² M
given: [H₃O⁺] · found: pH 12 · basic

One edge: −log along the top. A basic solution still gets its pH from [H₃O⁺]. ✓
Dr. Karmach

Practice 2: from pH to [OH⁻]

hand soap solution: pH 9
measured at 25 °C

What is the soap solution's [OH⁻], in M?

  1. 1 × 10⁻⁹
  2. 1 × 10⁻⁵
  3. 1 × 10⁻²³
  4. 1 × 10⁵
Dr. Karmach

Practice 2 · answer: B

hand soap solution: pH 9
pOH = 14 − 9 = 5 · [OH⁻] = 1 × 10⁻⁵ M (answer B)

B: 14 − pH gives pOH 5, and pOH 5 means [OH⁻] = 1 × 10⁻⁵ M. A rebuilt [H₃O⁺] from the pH: 1 × 10⁻⁹ M is the hydronium, not the hydroxide. C multiplied by Kw instead of dividing: (1.0 × 10⁻¹⁴)(1 × 10⁻⁹) = 1 × 10⁻²³. D lost the minus sign: pOH 5 means 10⁻⁵, not 10⁵.

Kw checks it: (1 × 10⁻⁹)(1 × 10⁻⁵) = 1 × 10⁻¹⁴. Above pH 7, OH⁻ outnumbers H₃O⁺. ✓
Dr. Karmach

Practice 2: the route on the map

hand soap solution: pH 9
given: pH · found: pOH 5 · [OH⁻] = 1 × 10⁻⁵ M

Down the right edge with 14 − pH, then along the bottom with ten to the −pOH. ✓
Dr. Karmach

Practice 3: a pH with decimals

grapefruit juice: [H₃O⁺] = 6.3 × 10⁻⁴ M
measured at 25 °C

What is the pH of the grapefruit juice?

  1. 4
  2. −3.20
  3. 10.80
  4. 3.20
Dr. Karmach

Practice 3 · answer: D

grapefruit juice: [H₃O⁺] = 6.3 × 10⁻⁴ M
pH = −log(6.3 × 10⁻⁴) = 3.20 (answer D) · 2 significant figures ↔ 2 decimal places · acidic

D: the log key gives 3.2007, and 6.3 carries two significant figures, so the pH keeps two decimal places. A read the exponent alone, as if [H₃O⁺] were 1 × 10⁻⁴ M; 6.3 times that much H₃O⁺ pulls the pH below 4. B skipped the minus in −log: log(6.3 × 10⁻⁴) = −3.20. C reported the pOH: 14 − 3.20 = 10.80.

6.3 × 10⁻⁴ M lies between 1 × 10⁻⁴ M (pH 4) and 1 × 10⁻³ M (pH 3), and 3.20 falls between them. ✓
Dr. Karmach

Practice 3: the route on the map

grapefruit juice: [H₃O⁺] = 6.3 × 10⁻⁴ M
given: [H₃O⁺] · found: pH 3.20 · acidic

One edge, then the ladder. The coefficient 6.3 adds the decimals. ✓
Dr. Karmach

Practice 4: from [OH⁻] to pH

laundry detergent solution: [OH⁻] = 4.0 × 10⁻³ M
measured at 25 °C

What is the pH of the detergent solution?

  1. 11.60
  2. 2.40
  3. 11
  4. 16.40
Dr. Karmach

Practice 4 · answer: A

laundry detergent solution: [OH⁻] = 4.0 × 10⁻³ M
pOH = −log(4.0 × 10⁻³) = 2.40 · pH = 14.00 − 2.40 = 11.60 (answer A)

A: two moves, and 4.0 carries two significant figures, so both p-numbers keep two decimals. B stopped at the pOH: 2.40. C read the exponent alone: pOH 3, then 14 − 3 = 11, ignoring the 4.0. D added: 14 + 2.40 = 16.40, the same number Kw gives when multiplied instead of divided.

The Kw route agrees: [H₃O⁺] = 1.0 × 10⁻¹⁴ ÷ 4.0 × 10⁻³ = 2.5 × 10⁻¹² M, and −log gives 11.60. ✓
Dr. Karmach

Practice 4: the route on the map

laundry detergent solution: [OH⁻] = 4.0 × 10⁻³ M
given: [OH⁻] · found: pOH 2.40 · pH 11.60

Along the bottom with −log, then up the right edge with 14 − pOH. ✓
Dr. Karmach

Worked example 4: comparing two solutions

lemon juice: pH 2 · black coffee: pH 5
which holds more H₃O⁺? by what factor?

Two acidic drinks, three pH steps apart. Decide which side holds more H₃O⁺, then turn the pH gap into a factor.

Dr. Karmach

Worked example 4: solution

Lower pH, more H₃O⁺

Lemon juice sits lower on the ladder, so it is the more acidic of the two.

pH gap: 5 − 2 = 3 steps
lower pH → more H₃O⁺ → lemon juice
Dr. Karmach

Worked example 4: solution

Lower pH, more H₃O⁺

pH gap: 5 − 2 = 3 steps
lower pH → more H₃O⁺ → lemon juice
Each pH step is a factor of ten
factor = 10 × 10 × 10 = 1000
[H₃O⁺]: 1 × 10⁻² M vs 1 × 10⁻⁵ M · lemon juice holds 1000 times the H₃O⁺
Three whole steps means three factors of ten: the answer is 10³, never 3.
Dr. Karmach

Worked example 4: the route on the map

lemon juice: pH 2 · black coffee: pH 5
found: [H₃O⁺] 1 × 10⁻² M vs 1 × 10⁻⁵ M · lemon juice holds 1000 times the H₃O⁺

The ladder picks the more acidic drink; the top edge, run backward, gives the factor. ✓
Dr. Karmach

Practice 5

garden-soil extract: pH 9 · rainwater: [H₃O⁺] = 1 × 10⁻⁴ M · cleaning solution: pOH 3
all three at 25 °C

Which order runs from the most H₃O⁺ to the least?

  1. cleaner > rain > soil
  2. cleaner > soil > rain
  3. rain > soil > cleaner
  4. soil > rain > cleaner
Dr. Karmach

Practice 5 · answer: C

rain: 1 × 10⁻⁴ M → pH 4 · soil: pH 9 · cleaner: pH = 14 − 3 = 11
lowest pH holds the most H₃O⁺ · rain > soil > cleaner (answer C)

C: every reading on the pH ladder first, then lowest to highest. A read the cleaner's pOH 3 as a pH; pH = 14 − 3 = 11 puts it last. B ranks by the pH values backward: highest pH first means least H₃O⁺ first. D treated the rain's 10⁻⁴ M as OH⁻: 14 − 4 = 10 puts rain below soil; an H₃O⁺ concentration reads straight as pH 4.

Three different readings, one ladder: convert each to pH before any comparison.
Dr. Karmach

Practice 5: the route on the map

rain: [H₃O⁺] = 1 × 10⁻⁴ M · soil: pH 9 · cleaner: pOH 3
found: pH 4 · pH 9 · pH 14 − 3 = 11 · rain > soil > cleaner

Rain moves along the top, the cleaner up the right edge; one ladder then ranks all three. ✓
Dr. Karmach

4 · Electrolytes & Dissociation

Classify a solute as a strong electrolyte, a weak electrolyte, or a nonelectrolyte from its compound type, and write its dissociation equation with the right ions, coefficients, and charge sum.

Dr. Karmach

Inside a sports drink

The label lists sodium, potassium, chloride. In the bottle, each one travels through the water as a separate charged particle. Nerve and muscle signals run on these moving charges.

Dr. Karmach

Conduction needs moving charges

A solution conducts only if charged particles can move through it. What a solute becomes in water sets how strongly its solution conducts: all ions, a few ions, or no ions at all.

Dr. Karmach

Does it dissolve, and into what?

KBr(s) → K⁺(aq) + Br⁻(aq)
group 1: soluble · dissolves as separate ions · the bulb lights
AgI(s): stays solid
iodides are soluble except with Ag⁺, Hg₂²⁺, Pb²⁺ · almost no ions reach the water · the bulb stays dark
C₁₂H₂₂O₁₁(s) → C₁₂H₂₂O₁₁(aq)
table sugar: molecular · dissolves as whole molecules · the bulb stays dark

The solubility rules answer the first question: does it dissolve? The second question is what the dissolved solute becomes. Only ions carry current.

Dr. Karmach

Three classes of solute

strong electrolyte: dissolves entirely as ions
soluble ionic compounds (NaOH, KOH included) · the seven strong acids: HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ · HClO₃
weak electrolyte: a small fraction ionizes
weak acids and weak bases: HC₂H₃O₂ · NH₃; most molecules stay whole
nonelectrolyte: dissolves as whole molecules
other molecular compounds: sugar · ethanol; no ions, no conduction

An electrolyte releases ions in water, and its solution conducts. Compound type assigns the class. Acids and bases get strength lists of their own.

Dr. Karmach

Dissociation equations

NaCl(s) → Na⁺(aq) + Cl⁻(aq)
1 + 1 = 2 ions per formula unit · charge: (1+) + (1−) = 0
CaCl₂(s) → Ca²⁺(aq) + 2 Cl⁻(aq)
1 + 2 = 3 ions per formula unit · charge: (2+) + 2(1−) = 0

Water pulls an ionic solid apart into its separate ions: dissociation. Each ion keeps its identity and its charge. A subscript counts separate ions, so it becomes a coefficient.

Dr. Karmach

Polyatomic ions stay in one piece

Na₂SO₄(s) → 2 Na⁺(aq) + SO₄²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0

Dissociation separates cations from anions. It never breaks the bonds inside a polyatomic ion: sulfate enters the water whole, carrying its 2− charge.

Dr. Karmach

Weak electrolytes: partial ionization

HC₂H₃O₂(aq) ⇌ H⁺(aq) + C₂H₃O₂⁻(aq)
most molecules stay whole · each ionization: (1+) + (1−) = 0
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a weak base: only a few molecules react · charge: (1+) + (1−) = 0

A molecular acid or base ionizes: reaction with water makes new ions. A weak one barely reacts: a few molecules ionize, the rest stay whole. The double arrow marks an incomplete reaction.

Dr. Karmach

The method

  1. Classify the solute. Soluble ionic and strong acids: strong. Other acids and bases: weak. Other molecular: nonelectrolyte.
  2. Write what water makes. Separated ions, a few ions, or whole molecules.
  3. Check the charge sum. The ions must total zero.

Dr. Karmach

Guided example: barium hydroxide

Ba(OH)₂(s) stirred into water
given: barium hydroxide · wanted: class + the dissociation equation

Clear barium hydroxide solution, called baryta water, turns cloudy when breath is bubbled through it. Classify Ba(OH)₂ and write its dissociation equation.

Step 1 takes two questions: ionic or molecular? If ionic, soluble or not?

Dr. Karmach

Guided example: classify the solute

Ba(OH)₂(s) stirred into water
given: barium hydroxide · wanted: class + the dissociation equation

Step 1 · Classify the solute

ionic or molecular? Ba is a metal; OH⁻ is a polyatomic ion
move 1 · a metal with an anion · answer: ionic
Dr. Karmach

Guided example: classify the solute

Ba(OH)₂(s) stirred into water
given: barium hydroxide · wanted: class + the dissociation equation

Step 1 · Classify the solute

ionic or molecular? Ba is a metal; OH⁻ is a polyatomic ion
move 1 · a metal with an anion · answer: ionic
soluble? hydroxides: insoluble except group 1 and Ba²⁺
move 2 · the solubility rules · answer: soluble
Dr. Karmach

Guided example: classify the solute

Ba(OH)₂(s) stirred into water
given: barium hydroxide · wanted: class + the dissociation equation

Step 1 · Classify the solute

ionic or molecular? Ba is a metal; OH⁻ is a polyatomic ion
move 1 · a metal with an anion · answer: ionic
soluble? hydroxides: insoluble except group 1 and Ba²⁺
move 2 · the solubility rules · answer: soluble
Soluble and ionic: a strong electrolyte. The solubility rules decided it; most hydroxides stay solid, and Ba²⁺ is a named exception. ✓
Dr. Karmach

Guided example: write the ions

Ba(OH)₂(s) stirred into water
classified: soluble ionic → strong electrolyte

Step 2 · Write what water makes

The subscript outside the parentheses counts whole hydroxide ions: (OH)₂ means 2 OH⁻.

Ba(OH)₂(s) → Ba²⁺(aq) + 2 OH⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit · OH⁻ stays whole
Dr. Karmach

Guided example: write the ions

Ba(OH)₂(s) stirred into water
classified: soluble ionic → strong electrolyte
Step 2 · Write what water makes
Ba(OH)₂(s) → Ba²⁺(aq) + 2 OH⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit · OH⁻ stays whole
Step 3 · Check the charge sum
Ba(OH)₂(s) → Ba²⁺(aq) + 2 OH⁻(aq)
charge: (2+) + 2(1−) = 0 ✓
Dr. Karmach

Guided example: write the ions

Ba(OH)₂(s) stirred into water
classified: soluble ionic → strong electrolyte
Step 2 · Write what water makes
Ba(OH)₂(s) → Ba²⁺(aq) + 2 OH⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit · OH⁻ stays whole
Step 3 · Check the charge sum
Ba(OH)₂(s) → Ba²⁺(aq) + 2 OH⁻(aq)
charge: (2+) + 2(1−) = 0 ✓
One 2+ ion against two 1− ions cancels. Hydroxide leaves as one piece: its O and H never separate. ✓
Dr. Karmach

Guided example: the route on the chart

Ba(OH)₂(s) → Ba²⁺(aq) + 2 OH⁻(aq)
ionic: yes · soluble: yes · found: strong electrolyte, 3 ions per formula unit

Two yes answers on the ionic branch reach strong electrolyte. The acid questions never came up. ✓
Dr. Karmach

Practice 1: which one conducts

AgCl · CH₃OH · NaNO₃ · CaCO₃
silver chloride · methanol · sodium nitrate · calcium carbonate

Each substance is stirred into its own beaker of water. Which beaker lights a conductivity bulb brightly?

  1. AgCl
  2. CH₃OH
  3. NaNO₃
  4. CaCO₃
Dr. Karmach

Practice 1: answer C

NaNO₃(s) → Na⁺(aq) + NO₃⁻(aq) (answer C)
ionic, group 1: soluble · strong electrolyte · 1 + 1 = 2 ions · charge: (1+) + (1−) = 0

A is ionic, but Ag⁺ is a chloride exception: AgCl stays solid. B read methanol's OH as hydroxide; it is covalently bonded, and the molecules stay whole. D is ionic, but carbonates are insoluble except with group 1 and NH₄⁺.

Ionic is not enough: the compound must also dissolve. Only NaNO₃ passes both questions. ✓
Dr. Karmach

Worked example 1: magnesium chloride

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation

Road crews spread MgCl₂ as a de-icer, and it dissolves freely. Classify it and write the dissociation equation.

Dr. Karmach

Worked example 1: solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation

Step 1 · Classify the solute

A metal with a nonmetal: ionic. A soluble ionic compound is a strong electrolyte.

Dr. Karmach

Worked example 1: solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation
Step 1 · Classify the solute Step 2 · Write what water makes
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit

The subscript counts two separate chloride ions. Each one leaves the lattice on its own.

Dr. Karmach

Worked example 1: solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation
Step 1 · Classify the solute Step 2 · Write what water makes
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit
Step 3 · Check the charge sum
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
3 ions · charge: (2+) + 2(1−) = 0 ✓
Dr. Karmach

Worked example 1: solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation
Step 1 · Classify the solute Step 2 · Write what water makes
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit
Step 3 · Check the charge sum
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
3 ions · charge: (2+) + 2(1−) = 0 ✓
The solid is neutral, so the ions it releases must cancel: one 2+ against two 1−. A nonzero sum marks a wrong formula or a wrong coefficient. ✓
Dr. Karmach

Worked example 2: Na₂CO₃, NH₃, C₂H₅OH

Na₂CO₃ · NH₃ · C₂H₅OH
washing soda · household ammonia · ethanol · wanted: each class + what each solution contains

All three dissolve freely in water. Classify each and write what its solution contains.

Dr. Karmach

Worked example 2: classifying

Na₂CO₃ · NH₃ · C₂H₅OH
washing soda · household ammonia · ethanol

Step 1 · Classify the solute

solute type class
Na₂CO₃ soluble ionic compound strong electrolyte
NH₃ molecular base, not an ionic hydroxide weak electrolyte
C₂H₅OH molecular, neither acid nor base nonelectrolyte
Dr. Karmach

Worked example 2: classifying

Na₂CO₃ · NH₃ · C₂H₅OH
washing soda · household ammonia · ethanol

Step 1 · Classify the solute

solute type class
Na₂CO₃ soluble ionic compound strong electrolyte
NH₃ molecular base, not an ionic hydroxide weak electrolyte
C₂H₅OH molecular, neither acid nor base nonelectrolyte
All three bottles look identical. The compound type, not the appearance, separates them.
Dr. Karmach

Worked example 2: what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
Dr. Karmach

Worked example 2: what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a few ions · charge: (1+) + (1−) = 0 · most NH₃ molecules stay whole
Dr. Karmach

Worked example 2: what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a few ions · charge: (1+) + (1−) = 0 · most NH₃ molecules stay whole
C₂H₅OH(aq): dissolves as whole molecules
0 ions · the OH is covalently bonded, not OH⁻
Dr. Karmach

Worked example 2: what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a few ions · charge: (1+) + (1−) = 0 · most NH₃ molecules stay whole
C₂H₅OH(aq): dissolves as whole molecules
0 ions · the OH is covalently bonded, not OH⁻
Three clear solutions, three bulb readings: bright, dim, dark. ✓
Dr. Karmach

Worked example 2: the route on the chart

Na₂CO₃ · NH₃ · C₂H₅OH
Na₂CO₃: ionic, soluble · NH₃: not ionic, not on the acid list, a base · C₂H₅OH: every answer no

Three solutes leave by three exits. Only the ionic one needed the solubility rules. ✓
Dr. Karmach

Your turn: magnesium nitrate

Mg(NO₃)₂(s) dissolved in water
given: a soluble ionic compound · nitrate: NO₃⁻
step work result
1 · classify the solute soluble ionic compound electrolyte
2 · write what water makes Mg(NO₃)₂(s) → Mg²⁺(aq) + ions per formula unit:
3 · check the charge sum (2+) + 2(1−) =

Complete the classification and the equation.

Dr. Karmach

Your turn: magnesium nitrate

Mg(NO₃)₂(s) dissolved in water
given: a soluble ionic compound · nitrate: NO₃⁻
step work result
1 · classify the solute soluble ionic compound electrolyte
2 · write what water makes Mg(NO₃)₂(s) → Mg²⁺(aq) + ions per formula unit:
3 · check the charge sum (2+) + 2(1−) =

Complete the classification and the equation.

Mg(NO₃)₂(s) → Mg²⁺(aq) + 2 NO₃⁻(aq)
strong electrolyte · 1 + 2 = 3 ions · charge: (2+) + 2(1−) = 0 · each nitrate leaves whole
Dr. Karmach

Where this goes wrong

Reading a subscript as a bonded pair. CaCl₂ never releases a Cl₂²⁻ unit. The subscript counts separate ions: Ca²⁺ + 2 Cl⁻ makes 1 + 2 = 3 ions, not 1 + 1 = 2.
Breaking a polyatomic ion into atoms. Na₂CO₃ gives 2 Na⁺ + CO₃²⁻ = 3 ions, never 2 + 1 + 3 = 6 pieces. Dissociation separates ions; it does not break the bonds inside one.
Calling sugar a weak electrolyte. Weak means a few ions form. Sugar forms none: its solution conducts no better than pure water. Nonelectrolyte.
Reading a molecular OH as hydroxide. Ethanol's OH is covalently bonded and stays put. Only ionic hydroxides such as NaOH release OH⁻.
Dr. Karmach

Practice 2

K₃PO₄ dissolved in water
given: a soluble ionic compound · phosphate: PO₄³⁻

Fertilizer-grade potassium phosphate dissolves freely in water. Which statement classifies it and describes what its solution contains?

  1. Weak electrolyte: a salt built around a polyatomic ion dissociates only partially
  2. Strong electrolyte: it dissociates completely into 3 K⁺ and PO₄³⁻, four ions per formula unit
  3. Strong electrolyte: it dissociates completely into K₃⁺ and PO₄³⁻, two ions per formula unit
  4. Nonelectrolyte: it dissolves as intact, neutral K₃PO₄ molecules
Dr. Karmach

Practice 2: answer B

K₃PO₄(s) → 3 K⁺(aq) + PO₄³⁻(aq) (answer B)
3 + 1 = 4 ions · charge: 3(1+) + (3−) = 0

A: solubility decides, not the anion; a soluble salt dissociates completely, polyatomic ion or not. C: the subscript counts three separate K⁺ ions; no K₃⁺ unit exists, and 1 + 1 = 2 undercounts the ions. D: an ionic compound has no molecules; only separated ions enter the water.

Four ions from one formula unit, and the charges cancel: 3(1+) + (3−) = 0. ✓
Dr. Karmach

Practice 3: smelling salts

(NH₄)₂CO₃ dissolved in water
ammonium carbonate, the compound in smelling salts

Which equation shows ammonium carbonate dissolving in water?

  1. (NH₄)₂CO₃(s) ⇌ 2 NH₄⁺(aq) + CO₃²⁻(aq)
  2. (NH₄)₂CO₃(s) → NH₄⁺(aq) + CO₃²⁻(aq)
  3. (NH₄)₂CO₃(s) → (NH₄)₂²⁺(aq) + CO₃²⁻(aq)
  4. (NH₄)₂CO₃(s) → 2 NH₄⁺(aq) + C⁴⁺(aq) + 3 O²⁻(aq)
  5. (NH₄)₂CO₃(s) → 2 NH₄⁺(aq) + CO₃²⁻(aq)
Dr. Karmach

Practice 3: answer E

(NH₄)₂CO₃(s) → 2 NH₄⁺(aq) + CO₃²⁻(aq) (answer E)
NH₄⁺ compounds: soluble · strong electrolyte · 2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0

A used the weak-base arrow of NH₃; an ammonium salt dissociates completely. B dropped the coefficient: (1+) + (2−) = 1−. C welded two NH₄⁺ into one ion. D broke carbonate into atoms, though 2(1+) + (4+) + 3(2−) = 0.

Both polyatomic ions leave whole; NH₄⁺ makes the salt ionic and soluble. ✓
Dr. Karmach

Worked example 3: ion concentrations

0.100 M AlBr₃ dissolved in water
M, molarity = mol of solute per liter of solution · wanted: the molarity of Br⁻

Aluminum bromide dissolves freely. Every formula unit that dissolves releases its ions into the same liter. Find the concentration of Br⁻ in the solution.

Dr. Karmach

Worked example 3: solution

0.100 M AlBr₃ → ? M Br⁻
M = mol per liter of solution

Step 1 · Classify the solute

A metal with a nonmetal: soluble ionic, a strong electrolyte. Every formula unit dissociates.

Dr. Karmach

Worked example 3: solution

0.100 M AlBr₃ → ? M Br⁻
M = mol per liter of solution
Step 1 · Classify the solute Step 2 · Write what water makes Step 3 · Check the charge sum
AlBr₃(s) → Al³⁺(aq) + 3 Br⁻(aq)
1 + 3 = 4 ions · charge: (3+) + 3(1−) = 0 ✓
Dr. Karmach

Worked example 3: solution

0.100 M AlBr₃ → ? M Br⁻
M = mol per liter of solution
Step 1 · Classify the solute Step 2 · Write what water makes Step 3 · Check the charge sum
AlBr₃(s) → Al³⁺(aq) + 3 Br⁻(aq)
1 + 3 = 4 ions · charge: (3+) + 3(1−) = 0 ✓
Ion molarity · multiply by the coefficient

Each liter holds 0.100 mol of dissolved AlBr₃, and each mole releases 3 mol of Br⁻.

0.100 mol AlBr₃ × 3 mol Br⁻1 mol AlBr₃ = 0.300 mol Br⁻ per liter = 0.300 M
Dr. Karmach

Worked example 3: solution

0.100 M AlBr₃ → ? M Br⁻
M = mol per liter of solution
Step 1 · Classify the solute Step 2 · Write what water makes Step 3 · Check the charge sum
AlBr₃(s) → Al³⁺(aq) + 3 Br⁻(aq)
1 + 3 = 4 ions · charge: (3+) + 3(1−) = 0 ✓
Ion molarity · multiply by the coefficient

Each liter holds 0.100 mol of dissolved AlBr₃, and each mole releases 3 mol of Br⁻.

0.100 mol AlBr₃ × 3 mol Br⁻1 mol AlBr₃ = 0.300 mol Br⁻ per liter = 0.300 M
The subscript became a concentration ratio: 0.300 M Br⁻ against 0.100 M Al³⁺.
Dr. Karmach

Practice 4: an etching bath

0.15 M FeCl₃ dissolved in water
given: 0.15 M FeCl₃ · wanted: the molarity of Cl⁻

Circuit-board etching baths use iron(III) chloride. A bath is mixed to 0.15 M FeCl₃. What is the molarity of Cl⁻ in the bath?

  1. 0.60
  2. 0.45
  3. 0.15
  4. 0.050
Dr. Karmach

Practice 4: answer B

FeCl₃(s) → Fe³⁺(aq) + 3 Cl⁻(aq)
soluble ionic: strong electrolyte · 1 + 3 = 4 ions · charge: (3+) + 3(1−) = 0 ✓
0.15 mol FeCl₃ × 3 mol Cl⁻1 mol FeCl₃ = 0.45 mol Cl⁻ per liter = 0.45 M (answer B)

A counted every ion: 0.15 × 4 = 0.60 M is Fe³⁺ and Cl⁻ together. C skipped the ratio: 0.15 × 1 = 0.15 M is the Fe³⁺ molarity. D flipped the ratio: 0.15 ÷ 3 = 0.050 M.

Three chlorides per formula unit: the chloride runs at three times the salt, 3 × 0.15 = 0.45 M. ✓
Dr. Karmach

Practice 5

Fe₂(SO₄)₃ dissolved in water
given: 0.60 M SO₄²⁻ required · wanted: the molarity of Fe₂(SO₄)₃

A water plant's dosing tank must reach 0.60 M sulfate ion, supplied by dissolving iron(III) sulfate. What molarity of Fe₂(SO₄)₃ does the tank need?

  1. 0.30
  2. 1.8
  3. 0.60
  4. 0.20
Dr. Karmach

Practice 5: answer D

Fe₂(SO₄)₃(s) → 2 Fe³⁺(aq) + 3 SO₄²⁻(aq)
2 + 3 = 5 ions · charge: 2(3+) + 3(2−) = 0 ✓
0.60 mol SO₄²⁻ × 1 mol Fe₂(SO₄)₃3 mol SO₄²⁻ = 0.20 mol Fe₂(SO₄)₃ per liter = 0.20 M (answer D)

C skipped the ratio: 0.60 × 1 = 0.60 M assumes one sulfate per formula unit. B flipped the ratio: 0.60 × 3 = 1.8 M, a tank at 1.8 × 3 = 5.4 M sulfate. A used iron's subscript: 0.60 ÷ 2 = 0.30 M.

Each formula unit releases three sulfates, so the salt runs at one third of the target: 3 × 0.20 = 0.60 M sulfate ✓.
Dr. Karmach

5 · Titration Calculations

Find an unknown acid concentration from a titration by counting the titrant's millimoles, dividing out the balanced equation's base-to-acid ratio, and dividing by the acid's volume; the milliliters cancel.

Dr. Karmach

Reading the acid in vinegar

Add a drop of dye to vinegar, then drip in a known base until the color just changes. The base you used measures the acid.

Dr. Karmach

Acid plus base makes salt and water

HCl(aq) + NaOH(aq) → NaCl(aq) + H₂O(l)
acid + base → salt + water · the H⁺ and the OH⁻ join as H₂O

An acid and a base neutralize each other. Each H⁺ from the acid meets one OH⁻ from the base. The ions left over form a salt.

Complete it: HNO₃(aq) + KOH(aq) → ?

Dr. Karmach

Acid plus base makes salt and water

HCl(aq) + NaOH(aq) → NaCl(aq) + H₂O(l)
acid + base → salt + water · the H⁺ and the OH⁻ join as H₂O

An acid and a base neutralize each other. Each H⁺ from the acid meets one OH⁻ from the base. The ions left over form a salt.

Complete it: HNO₃(aq) + KOH(aq) → ?

HNO₃(aq) + KOH(aq) → KNO₃(aq) + H₂O(l)
K⁺ from the base · NO₃⁻ from the acid · one H⁺ meets one OH⁻
Dr. Karmach

The equivalence point

Add a known base to an acid until an indicator flips; this addition is a titration. At the flip, the equivalence point, moles of OH⁻ added equal moles of H⁺ available.

Dr. Karmach

End point and equivalence point

equivalence point: moles of H⁺ = moles of OH⁻
end point: the indicator changes color · a good indicator changes within one drop of the equivalence point

The equivalence point cannot be seen. The indicator's color change, the end point, marks it. The buret reading at the end point is the volume the calculation uses.

Dr. Karmach

Molarity is a conversion factor

0.250 M NaOH = 0.250 mol per 1 L = 0.250 mmol per 1 mL
mol and L both shrink by 1000 to mmol and mL · the ratio stays 0.250
0.250 mmol NaOH1 mL or 1 mL0.250 mmol NaOH · pick the one that cancels the given unit

Molarity links volume and moles, either way up. How many millimoles of NaOH are in 12.00 mL of 0.250 M NaOH?

Dr. Karmach

Molarity is a conversion factor

0.250 M NaOH = 0.250 mol per 1 L = 0.250 mmol per 1 mL
mol and L both shrink by 1000 to mmol and mL · the ratio stays 0.250
0.250 mmol NaOH1 mL or 1 mL0.250 mmol NaOH · pick the one that cancels the given unit

Molarity links volume and moles, either way up. How many millimoles of NaOH are in 12.00 mL of 0.250 M NaOH?

12.00 mL × 0.250 mmol NaOH1 mL = 3.00 mmol NaOH · in liters: 0.01200 L × 0.250 mol/L = 0.00300 mol, the same amount
Dr. Karmach

Equal millimoles in a 1:1 reaction

0.200 M × 25.00 mL = 5.00 mmol
molarity × volume, with volume in mL, counts millimoles
Macid · Vacid = Mbase · Vbase
1 : 1 acid to base · both volumes in mL, so the mL cancel

Moles equal molarity times volume. With volume in milliliters, that product counts millimoles. When an acid and base react one-to-one, their millimoles are equal.

Dr. Karmach

Polyprotic acids need the mole ratio

Macid = Mbase · Vbase ÷ (ratio · Vacid)
ratio = base units per acid unit · the mL cancel, so no liter step

A diprotic acid gives two H⁺ per unit; a triprotic gives three. Each H⁺ takes one OH⁻, so the balanced equation's coefficients set the base-to-acid ratio.

memory hook: count the H's written first
HCl 1 · H₂SO₄ 2 · H₃PO₄ 3 · that many NaOH per acid
Dr. Karmach

The method

  1. Moles of the known solution: molarity × mL gives millimoles.
  2. Apply the mole ratio: cross to the other substance with the balanced equation.
  3. Divide to finish: by its volume for a molarity, or by its molarity for a volume.
Dr. Karmach

The route through a titration problem

Start from the solution whose molarity and volume are both known. The balanced equation carries its millimoles across. The wanted quantity picks the exit.

Dr. Karmach

Guided example: a KOH solution

HNO₃(aq) + KOH(aq) → KNO₃(aq) + H₂O(l)
given: 15.00 mL KOH titrated by 18.60 mL of 0.100 M HNO₃ · wanted: M of the KOH

A 15.00 mL sample of potassium hydroxide solution is titrated with 0.100 M HNO₃. The indicator changes color after 18.60 mL of acid. Find the molarity of the KOH.

Name the known solution first: the one with both its molarity and its volume given.

Dr. Karmach

Guided example: solution

HNO₃(aq) + KOH(aq) → KNO₃(aq) + H₂O(l)
given: 15.00 mL KOH · 18.60 mL of 0.100 M HNO₃ · wanted: M of the KOH

The acid in the buret is the known solution: 18.60 mL and 0.100 M are both given. Three moves follow, one per method step.

Dr. Karmach

Guided example: solution

HNO₃(aq) + KOH(aq) → KNO₃(aq) + H₂O(l)
given: 15.00 mL KOH · 18.60 mL of 0.100 M HNO₃ · wanted: M of the KOH
Step 1 · Moles of the known solution
18.60 mL acid × 0.100 mmol HNO₃1 mL acid = 1.86 mmol HNO₃
Dr. Karmach

Guided example: solution

HNO₃(aq) + KOH(aq) → KNO₃(aq) + H₂O(l)
given: 15.00 mL KOH · 18.60 mL of 0.100 M HNO₃ · wanted: M of the KOH
Step 1 · Moles of the known solution
18.60 mL acid × 0.100 mmol HNO₃1 mL acid = 1.86 mmol HNO₃
Step 2 · Apply the mole ratio

The coefficients are 1 and 1: one KOH for each HNO₃, so the sample held 1.86 mmol KOH.

Dr. Karmach

Guided example: solution

HNO₃(aq) + KOH(aq) → KNO₃(aq) + H₂O(l)
given: 15.00 mL KOH · 18.60 mL of 0.100 M HNO₃ · wanted: M of the KOH
Step 1 · Moles of the known solution
18.60 mL acid × 0.100 mmol HNO₃1 mL acid = 1.86 mmol HNO₃
Step 2 · Apply the mole ratio Step 3 · Divide to finish
M = 1.86 mmol KOH15.00 mL base = 0.124 M KOH
Dr. Karmach

Guided example: solution

HNO₃(aq) + KOH(aq) → KNO₃(aq) + H₂O(l)
given: 15.00 mL KOH · 18.60 mL of 0.100 M HNO₃ · wanted: M of the KOH
Step 1 · Moles of the known solution
18.60 mL acid × 0.100 mmol HNO₃1 mL acid = 1.86 mmol HNO₃
Step 2 · Apply the mole ratio Step 3 · Divide to finish
M = 1.86 mmol KOH15.00 mL base = 0.124 M KOH
It took more acid (18.60 mL) than there was base (15.00 mL), so the base is more concentrated than the acid's 0.100 M: 0.124 M ✓
Dr. Karmach

Guided example: the route on the map

HNO₃(aq) + KOH(aq) → KNO₃(aq) + H₂O(l)
given: 18.60 mL of 0.100 M HNO₃ · 15.00 mL KOH · found: 0.124 M KOH

The known solution is the acid. Its 1.86 mmol cross the 1 : 1 ratio, and the KOH's own 15.00 mL give the molarity. ✓
Dr. Karmach

Worked example 1: a one-to-one titration

HCl + NaOH → NaCl + H₂O
given: 20.00 mL HCl titrated by 25.00 mL of 0.200 M NaOH · wanted: M of the HCl

A 20.00 mL sample of hydrochloric acid of unknown concentration is titrated with 0.200 M NaOH. The indicator changes color after 25.00 mL of base. Find the concentration of the acid.

Set it up: the base's millimoles, the 1:1 ratio, then divide by the acid's volume.

Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 20.00 mL HCl · 25.00 mL of 0.200 M NaOH · wanted: M of the HCl

Three moves: the titrant's millimoles, the one-to-one ratio, then divide by the acid's volume.

Step 1 · Moles of the known solution

The base's molarity is 0.200 mmol per mL. Its volume converts to millimoles; the mL cancel:

25.00 mL base × 0.200 mmol NaOH1 mL base = 5.00 mmol NaOH
Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 20.00 mL HCl · 25.00 mL of 0.200 M NaOH · wanted: M of the HCl
Step 1 · Moles of the known solution
25.00 mL base × 0.200 mmol NaOH1 mL base = 5.00 mmol NaOH
Step 2 · Apply the mole ratio

HCl and NaOH react one-to-one, so the acid supplied the same count: 5.00 mmol HCl.

Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 20.00 mL HCl · 25.00 mL of 0.200 M NaOH · wanted: M of the HCl
Step 1 · Moles of the known solution
25.00 mL base × 0.200 mmol NaOH1 mL base = 5.00 mmol NaOH
Step 2 · Apply the mole ratio Step 3 · Divide to finish

The acid's millimoles over its volume give the molarity. Millimoles per milliliter is moles per liter:

M = 5.00 mmol HCl20.00 mL acid = 0.250 M HCl
Dr. Karmach

Worked example 1: solution

HCl + NaOH → NaCl + H₂O
given: 20.00 mL HCl · 25.00 mL of 0.200 M NaOH · wanted: M of the HCl
Step 1 · Moles of the known solution
25.00 mL base × 0.200 mmol NaOH1 mL base = 5.00 mmol NaOH
Step 2 · Apply the mole ratio Step 3 · Divide to finish
M = 5.00 mmol HCl20.00 mL acid = 0.250 M HCl
The base's 25.00 mL slightly topped the acid's 20.00 mL at 0.200 M, so the acid runs a little higher: 0.250 M ✓
Dr. Karmach

Worked example 1: the route on the map

HCl + NaOH → NaCl + H₂O
given: 25.00 mL of 0.200 M NaOH · 20.00 mL HCl · found: 0.250 M HCl

Here the base in the buret is the known solution. Same chain, same exit: ÷ the acid's own 20.00 mL. ✓
Dr. Karmach

Practice 1

HClO₄(aq) + NaOH(aq) → NaClO₄(aq) + H₂O(l)
titrant 0.100 M NaOH · sample 16.00 mL perchloric acid

A 16.00 mL sample of perchloric acid needs 22.40 mL of 0.100 M NaOH to reach the end point. What is the molarity of the HClO₄?

  1. 0.0714
  2. 0.000140
  3. 0.0583
  4. 0.140
Dr. Karmach

Practice 1 answer: D

HClO₄(aq) + NaOH(aq) → NaClO₄(aq) + H₂O(l)
given: 16.00 mL HClO₄ · 22.40 mL of 0.100 M NaOH · wanted: M of the HClO₄
22.40 mL base × 0.100 mmol NaOH1 mL base × 1 mmol HClO₄1 mmol NaOH = 2.24 mmol HClO₄, then ÷ 16.00 mL acid = 0.140 M · answer D

A swapped the volumes: 0.100 × 16.00 ÷ 22.40 = 0.0714 M. B put the base's volume in liters but left the acid's in mL: 0.100 × 0.02240 ÷ 16.00 = 0.000140. C divided by the total volume in the flask: 2.24 ÷ 38.40 = 0.0583 M.

More base than acid by volume, so the acid is more concentrated than the base's 0.100 M: 0.140 M ✓
Dr. Karmach

Practice 1: the route on the map

HClO₄(aq) + NaOH(aq) → NaClO₄(aq) + H₂O(l)
given: 22.40 mL of 0.100 M NaOH · 16.00 mL HClO₄ · found: 0.140 M HClO₄

The molarity exit divides by the acid's own 16.00 mL, never by the 38.40 mL of mixture in the flask. ✓
Dr. Karmach

Worked example 2: a diprotic acid

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ titrated by 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄

A 20.00 mL sample of sulfuric acid is titrated with 0.250 M NaOH, and the indicator changes color after 32.00 mL of base. Sulfuric acid is diprotic: each unit gives two H⁺. Find its concentration.

A tempting shortcut: carry the base's millimoles straight to the acid's volume. Test it against the balanced equation.

Dr. Karmach

Worked example 2: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ · 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄

Three moves, but the base-to-acid ratio is no longer one.

Step 1 · Moles of the known solution

The base delivers 0.250 mmol per mL, so 32.00 mL is 8.00 mmol NaOH.

Dr. Karmach

Worked example 2: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ · 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄
Step 1 · Moles of the known solution The tempting shortcut

Carry the base's millimoles straight to the acid's volume, as if the ratio were one:

M = 8.00 mmol NaOH20.00 mL acid = 0.400 M ✗
Dr. Karmach

Worked example 2: solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ · 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄
Step 1 · Moles of the known solution The tempting shortcut

Carry the base's millimoles straight to the acid's volume, as if the ratio were one:

M = 8.00 mmol NaOH20.00 mL acid = 0.400 M ✗
Each H₂SO₄ gives two H⁺, so those 8.00 mmol OH⁻ neutralized only half as many acid units. ✗
Dr. Karmach

Worked example 2: the mole ratio

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ · 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄

Step 2 · Apply the mole ratio Step 3 · Divide to finish

The ratio, 1 H₂SO₄ per 2 NaOH, halves the count; the acid's volume then divides:

32.00 mL base × 0.250 mmol NaOH1 mL base × 1 mmol H₂SO₄2 mmol NaOH = 4.00 mmol H₂SO₄, then ÷ 20.00 mL acid = 0.200 M H₂SO₄
Dr. Karmach

Worked example 2: the mole ratio

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 20.00 mL H₂SO₄ · 32.00 mL of 0.250 M NaOH · wanted: M of the H₂SO₄
Step 2 · Apply the mole ratio Step 3 · Divide to finish
32.00 mL base × 0.250 mmol NaOH1 mL base × 1 mmol H₂SO₄2 mmol NaOH = 4.00 mmol H₂SO₄, then ÷ 20.00 mL acid = 0.200 M H₂SO₄
The 2:1 ratio halves the acid's millimoles, so its concentration is half the shortcut's guess: 0.200 M, not 0.400 M ✓
Dr. Karmach

Worked example 2: the route on the map

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 32.00 mL of 0.250 M NaOH · 20.00 mL H₂SO₄ · found: 0.200 M H₂SO₄

The same route as a 1 : 1 titration. Only the ratio step changes: 1 H₂SO₄ per 2 NaOH halves 8.00 mmol to 4.00 mmol. ✓
Dr. Karmach

Take-home: a polyprotic acid is not 1:1

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 32.00 mL of 0.250 M NaOH · 20.00 mL H₂SO₄
M = 8.00 mmol NaOH20.00 mL acid = 0.400 M ✗ · counts each H₂SO₄ as one H⁺
32.00 mL base × 0.250 mmol NaOH1 mL base × 1 mmol H₂SO₄2 mmol NaOH ÷ 20.00 mL acid = 0.200 M ✓

A diprotic acid feeds two H⁺, a triprotic three. The balanced equation's ratio divides the base's millimoles before the volume does. Skip it and every diprotic answer comes out doubled.

Dr. Karmach

Your turn: sulfuric acid and KOH

H₂SO₄ + 2 KOH → K₂SO₄ + 2 H₂O
given: 40.00 mL of 0.150 M KOH · 25.00 mL H₂SO₄ · wanted: M of the H₂SO₄

It takes 40.00 mL of 0.150 M KOH to titrate 25.00 mL of H₂SO₄. Fill the molarity, the 2:1 ratio, and the acid's volume, then compute:

40.00 mL base × mmol KOH1 mL base × 1 mmol H₂SO₄ mmol KOH = mmol H₂SO₄, then ÷ mL acid = M
Dr. Karmach

Your turn: sulfuric acid and KOH

H₂SO₄ + 2 KOH → K₂SO₄ + 2 H₂O
given: 40.00 mL of 0.150 M KOH · 25.00 mL H₂SO₄ · wanted: M of the H₂SO₄

It takes 40.00 mL of 0.150 M KOH to titrate 25.00 mL of H₂SO₄. Fill the molarity, the 2:1 ratio, and the acid's volume, then compute:

40.00 mL base × mmol KOH1 mL base × 1 mmol H₂SO₄ mmol KOH = mmol H₂SO₄, then ÷ mL acid = M
40.00 mL base × 0.150 mmol KOH1 mL base × 1 mmol H₂SO₄2 mmol KOH = 3.00 mmol H₂SO₄, then ÷ 25.00 mL acid = 0.120 M H₂SO₄
Dr. Karmach

Where this goes wrong

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 32.00 mL of 0.250 M NaOH · 20.00 mL H₂SO₄ · correct: 8.00 mmol NaOH → 4.00 mmol H₂SO₄ → 0.200 M
Treating the diprotic acid as 1:1. 8.00 mmol ÷ 20.00 mL = 0.400 M, double the truth. Each H₂SO₄ gives two H⁺, so divide the base's millimoles by 2 first.
Multiplying by the ratio instead of dividing. 2 × 8.00 ÷ 20.00 = 0.800 M. Each acid unit uses up two OH⁻, so there are fewer acid units than base units: the 2 divides.
Swapping the two volumes. Pairing 0.250 M with 20.00 mL gives 0.250 × 20.00 ÷ 2 ÷ 32.00 = 0.0781 M. Each molarity multiplies its own solution's volume.
Dr. Karmach

Practice 2

H₂C₂O₄ + 2 NaOH → Na₂C₂O₄ + 2 H₂O
titrant 0.125 M NaOH · sample 18.00 mL oxalic acid

It takes 28.80 mL of 0.125 M NaOH to reach the color change while titrating 18.00 mL of oxalic acid. What is the molarity of the oxalic acid?

  1. 1.80
  2. 0.100
  3. 0.200
  4. 0.400
Dr. Karmach

Practice 2 answer: B

H₂C₂O₄ + 2 NaOH → Na₂C₂O₄ + 2 H₂O
given: 18.00 mL H₂C₂O₄ · 28.80 mL of 0.125 M NaOH · wanted: M of the H₂C₂O₄
28.80 mL base × 0.125 mmol NaOH1 mL base × 1 mmol H₂C₂O₄2 mmol NaOH = 1.80 mmol H₂C₂O₄, then ÷ 18.00 mL acid = 0.100 M · answer B

A stopped at 1.80 mmol of oxalic acid, before dividing by its 18.00 mL. C ignored the 2:1 ratio: 3.60 ÷ 18.00 = 0.200 M. D multiplied by the ratio: 2 × 3.60 ÷ 18.00 = 0.400 M.

Two NaOH per oxalic acid, so the acid holds half the base's 3.60 mmol: 1.80 mmol in 18.00 mL is 0.100 M ✓
Dr. Karmach

Practice 2: the route on the map

H₂C₂O₄ + 2 NaOH → Na₂C₂O₄ + 2 H₂O
given: 28.80 mL of 0.125 M NaOH · 18.00 mL H₂C₂O₄ · found: 0.100 M H₂C₂O₄

3.60 mmol NaOH cross the 2 : 1 ratio as 1.80 mmol H₂C₂O₄. The acid's own 18.00 mL finish the molarity. ✓
Dr. Karmach

Worked example 3: volume of base for a triprotic acid

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · titrant 0.150 M NaOH · wanted: mL of NaOH

A 25.00 mL sample of 0.0600 M phosphoric acid is titrated with 0.150 M NaOH. Phosphoric acid is triprotic: each unit gives three H⁺. What volume of base reaches the color change?

A common first attempt divides by 3 out of habit. Test it against the protons.

Dr. Karmach

Worked example 3: solution

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · 0.150 M NaOH · wanted: mL of NaOH

Here the acid is the known solution, and the base's volume is the unknown.

Step 1 · Moles of the known solution

25.00 mL of 0.0600 M H₃PO₄ holds 25.00 × 0.0600 = 1.50 mmol H₃PO₄.

Dr. Karmach

Worked example 3: solution

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · 0.150 M NaOH · wanted: mL of NaOH
Step 1 · Moles of the known solution A common first attempt
1.50 mmol ÷ 3 = 0.500 mmol NaOH → 0.500 ÷ 0.150 = 3.33 mL ✗
Each H₃PO₄ carries three H⁺, and each H⁺ takes one OH⁻. The base's millimoles are three times the acid's, not a third. ✗
Dr. Karmach

Worked example 3: the mole ratio

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · 0.150 M NaOH · wanted: mL of NaOH

Step 2 · Apply the mole ratio Step 3 · Divide to finish

The ratio, 3 NaOH per H₃PO₄, triples the count; the base's molarity, upside down, turns millimoles into milliliters:

1.50 mmol H₃PO₄ × 3 mmol NaOH1 mmol H₃PO₄ × 1 mL base0.150 mmol NaOH = 30.0 mL NaOH
Dr. Karmach

Worked example 3: the mole ratio

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · 0.150 M NaOH · wanted: mL of NaOH
Step 2 · Apply the mole ratio Step 3 · Divide to finish
1.50 mmol H₃PO₄ × 3 mmol NaOH1 mmol H₃PO₄ × 1 mL base0.150 mmol NaOH = 30.0 mL NaOH
4.50 mmol of NaOH at 0.150 mmol per mL takes 30.0 mL, nine times the 3.33 mL guess ✓
Dr. Karmach

Worked example 3: the route on the map

H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O
given: 25.00 mL of 0.0600 M H₃PO₄ · 0.150 M NaOH · found: 30.0 mL NaOH

The acid is the known solution. The ratio triples 1.50 mmol to 4.50 mmol NaOH, and the volume exit divides by the base's 0.150 M. ✓
Dr. Karmach

Practice 3

H₂SO₄(aq) + 2 LiOH(aq) → Li₂SO₄(aq) + 2 H₂O(l)
titrant 0.300 M H₂SO₄ · sample 30.00 mL of 0.120 M LiOH

A spacecraft's CO₂ scrubber runs on lithium hydroxide solution. What volume of 0.300 M H₂SO₄, in mL, neutralizes 30.00 mL of 0.120 M LiOH?

  1. 12.0
  2. 24.0
  3. 6.00
  4. 15.0
Dr. Karmach

Practice 3 answer: C

H₂SO₄(aq) + 2 LiOH(aq) → Li₂SO₄(aq) + 2 H₂O(l)
given: 30.00 mL of 0.120 M LiOH · 0.300 M H₂SO₄ · wanted: mL of H₂SO₄
30.00 mL base × 0.120 mmol LiOH1 mL base × 1 mmol H₂SO₄2 mmol LiOH = 1.80 mmol H₂SO₄, then ÷ 0.300 mmol per mL acid = 6.00 mL · answer C

A ignored the 2 : 1 ratio: 3.60 ÷ 0.300 = 12.0 mL. B multiplied by the ratio: 2 × 3.60 ÷ 0.300 = 24.0 mL. D divided by the base's molarity instead of the acid's: 1.80 ÷ 0.120 = 15.0 mL.

The acid is 2.5 times as concentrated, and each H₂SO₄ takes two LiOH: 30.00 mL ÷ 2.5 ÷ 2 = 6.00 mL ✓
Dr. Karmach

Practice 3: the route on the map

H₂SO₄(aq) + 2 LiOH(aq) → Li₂SO₄(aq) + 2 H₂O(l)
given: 30.00 mL of 0.120 M LiOH · 0.300 M H₂SO₄ · found: 6.00 mL H₂SO₄

The base is the known solution this time. The ratio halves 3.60 mmol to 1.80 mmol, and the volume exit divides by the acid's own 0.300 M. ✓
Dr. Karmach

Practice 4

H₃C₆H₅O₇ + 3 NaOH → Na₃C₆H₅O₇ + 3 H₂O
given: 26.40 mL of 0.120 M NaOH · citric acid 192.12 g/mol · wanted: g of citric acid

A powdered drink mix is dissolved in water, and its citric acid takes 26.40 mL of 0.120 M NaOH to reach the color change. How many grams of citric acid did the sample hold?

  1. 0.203
  2. 0.609
  3. 1.06
  4. 203
  5. 1.83
Dr. Karmach

Practice 4 answer: A

H₃C₆H₅O₇ + 3 NaOH → Na₃C₆H₅O₇ + 3 H₂O
26.40 mL of 0.120 M NaOH · citric acid 192.12 g/mol
26.40 mL base × 0.120 mmol NaOH1 mL base × 1 mmol acid3 mmol NaOH = 1.056 mmol acid
Dr. Karmach

Practice 4 answer: A

H₃C₆H₅O₇ + 3 NaOH → Na₃C₆H₅O₇ + 3 H₂O
26.40 mL of 0.120 M NaOH · citric acid 192.12 g/mol
26.40 mL base × 0.120 mmol NaOH1 mL base × 1 mmol acid3 mmol NaOH = 1.056 mmol acid
1.056 mmol × 1 mol1000 mmol × 192.12 g1 mol = 0.203 g · answer A

B ignored the 3:1 ratio: 3.168 mmol → 0.609 g. C stopped at 1.06 mmol, before the molar mass. D skipped mmol → mol: 1.056 × 192.12 = 203 g. E multiplied by the ratio: 9.504 mmol → 1.83 g.

1.056 mmol is a third of 3.168: three NaOH per citric acid. 203 g would outweigh the sample. ✓
Dr. Karmach

Practice 4: the route on the map

H₃C₆H₅O₇ + 3 NaOH → Na₃C₆H₅O₇ + 3 H₂O
given: 26.40 mL of 0.120 M NaOH · citric acid 192.12 g/mol · found: 0.203 g

The grams exit: 1.056 mmol of acid is 0.001056 mol, and the molar mass turns moles into grams. ✓
Dr. Karmach

Practice 5

HCl(aq) + Ca(OH)₂(aq) → CaCl₂(aq) + H₂O(l)
skeleton, not yet balanced · titrant 0.05000 M HCl · sample 25.00 mL limewater

Limewater is a calcium hydroxide solution. A 25.00 mL sample takes 18.36 mL of 0.05000 M HCl to reach the end point. What is the molarity of the Ca(OH)₂?

  1. 0.03672
  2. 0.07344
  3. 0.01059
  4. 0.03404
  5. 0.01836
Dr. Karmach

Practice 5 answer: E

2 HCl(aq) + Ca(OH)₂(aq) → CaCl₂(aq) + 2 H₂O(l)
Ca: 1 = 1 ✓ · Cl: 2 = 2 ✓ · H: 4 = 4 ✓ · O: 2 = 2 ✓ · given: 18.36 mL of 0.05000 M HCl · 25.00 mL Ca(OH)₂

Balance first: each Ca(OH)₂ carries two OH⁻, so it takes 2 HCl.

Dr. Karmach

Practice 5 answer: E

2 HCl(aq) + Ca(OH)₂(aq) → CaCl₂(aq) + 2 H₂O(l)
Ca: 1 = 1 ✓ · Cl: 2 = 2 ✓ · H: 4 = 4 ✓ · O: 2 = 2 ✓ · given: 18.36 mL of 0.05000 M HCl · 25.00 mL Ca(OH)₂
18.36 mL acid × 0.05000 mmol HCl1 mL acid × 1 mmol Ca(OH)₂2 mmol HCl = 0.4590 mmol Ca(OH)₂, then ÷ 25.00 mL base = 0.01836 M · answer E

A skipped balancing and used 1 : 1: 0.9180 ÷ 25.00 = 0.03672 M. B multiplied by the ratio: 2 × 0.9180 ÷ 25.00 = 0.07344 M. C divided by the total volume: 0.4590 ÷ 43.36 = 0.01059 M. D swapped the volumes: 0.05000 × 25.00 ÷ 2 ÷ 18.36 = 0.03404 M.

Two OH⁻ per Ca(OH)₂, so the base holds half the acid's 0.9180 mmol: 0.4590 mmol in 25.00 mL is 0.01836 M ✓
Dr. Karmach

Practice 5: the route on the map

2 HCl(aq) + Ca(OH)₂(aq) → CaCl₂(aq) + 2 H₂O(l)
given: 18.36 mL of 0.05000 M HCl · 25.00 mL Ca(OH)₂ · found: 0.01836 M Ca(OH)₂

Balancing comes before the ratio step: 1 Ca(OH)₂ per 2 HCl. The chain then runs as usual and exits through the base's own 25.00 mL. ✓
Dr. Karmach

Check yourself

  1. A 1:1 titration takes 24.0 mL of 0.150 M NaOH to neutralize 20.0 mL of HCl. Set up Macid = Mbase · Vbase ÷ Vacid and find the HCl concentration.
  2. Phosphoric acid reacts as H₃PO₄ + 3 NaOH → Na₃PO₄ + 3 H₂O. Which number becomes the base-to-acid ratio in the denominator, and where does it come from?

Every calculation here counted moles with a concentration, then crossed substances with the balanced equation's ratio: the same mole-ratio bridge that drives reaction stoichiometry. A concentration is only another way to count the moles a reaction runs on.

Dr. Karmach

Can you…?

  • ☐ recognize acids and bases by their properties and define them by the Arrhenius and Brønsted-Lowry definitions?
  • ☐ identify the Brønsted-Lowry acid, base, and conjugate pairs in a reaction, and write a species' conjugate acid or base?
  • ☐ classify acids and bases as strong or weak, write their ionization with the correct arrow, and predict the products of neutralization and gas-forming reactions?
  • ☐ use K_w, pH = −log[H₃O⁺], pOH, and pH + pOH = 14 to convert among [H₃O⁺], [OH⁻], pH, and pOH and label a solution acidic, basic, or neutral?
  • ☐ find an unknown acid or base concentration from titration data?

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

Dr. Karmach

table end

table end