Chemical Bonding

Preparation for General Chemistry · Dr. Karmach

Dr. Karmach

By the end of this unit, you can…

  • Classify a compound's bonding as ionic, covalent, or both, and a bond as nonpolar covalent, polar covalent, or ionic from the electronegativity difference
  • Write Lewis symbols for atoms and ions and show the electron transfer that gives an ionic compound its formula
  • Draw Lewis structures for molecules and polyatomic ions, including multiple bonds, resonance forms, and the common octet exceptions
  • Use VSEPR to predict the shape and bond angle of a molecule with up to four electron domains
  • Combine bond polarity with shape to decide whether a molecule is polar
Dr. Karmach

Today's route 🗺️

  1. Electronegativity & Bond Type
  2. Lewis Structures
  3. Exceptions to the Octet Rule
  4. VSEPR & Molecular Shape
  5. Molecular Polarity
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1 · Electronegativity & Bond Type

Classify any bond as nonpolar covalent, polar covalent, or ionic from the electronegativity difference, and mark which atom carries the partial negative charge, then classify a whole compound's bonding as ionic, covalent, or both.

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Pulling on shared electrons

Two atoms pull on the same pair of electrons. Pull evenly, and it stays centered. Pull much harder, and one atom drags the pair over, or takes it.

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How a bond shares its electrons

A bond is a shared pair of electrons. Each atom pulls on that pair; the strength of the pull is its electronegativity. Equal pulls share equally; unequal pulls share unequally.

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Electronegativity and its trend

Electronegativity measures how strongly an atom pulls on shared electrons. It climbs across a row and up a column, peaking at fluorine. Metals sit low; nonmetals near fluorine sit high.

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From difference to bond type

Subtract the two electronegativities, larger minus smaller, and read the bond type off the continuum.

under 0.4: even sharing · 0.4 to 1.7: unequal sharing · past 1.7: transfer
nonpolar covalent · polar covalent · ionic · guidelines, not walls
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The method

  1. Find the electronegativity difference. Larger minus smaller.
  2. Place it on the continuum. Near zero, nonpolar covalent; moderate, polar covalent; large, ionic.
  3. Name the bond and mark the charges. δ− on the more electronegative atom, δ+ on its partner.
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Worked example 1: the Cl–Cl bond

Cl–Cl (the bond inside Cl₂ gas)
electronegativity: Cl = 3.16 · Cl = 3.16 · wanted: bond type

Chlorine gas is two chlorine atoms sharing one pair of electrons.

Classify the bond.

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Worked example 1: solution

Cl–Cl (the bond inside Cl₂ gas)
electronegativity: Cl = 3.16 · Cl = 3.16

Step 1 · Find the electronegativity difference

ΔEN = 3.16 − 3.16 = 0
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Worked example 1: solution

Cl–Cl (the bond inside Cl₂ gas)
electronegativity: Cl = 3.16 · Cl = 3.16
Step 1 · Find the electronegativity difference
ΔEN = 3.16 − 3.16 = 0
Step 2 · Place it on the continuum

A difference of zero sits at the far left: nonpolar covalent.

Dr. Karmach

Worked example 1: solution

Cl–Cl (the bond inside Cl₂ gas)
electronegativity: Cl = 3.16 · Cl = 3.16
Step 1 · Find the electronegativity difference
ΔEN = 3.16 − 3.16 = 0
Step 2 · Place it on the continuum Step 3 · Name the bond and mark the charges
Cl–Cl → nonpolar covalent
equal electronegativities · the pair sits centered · no partial charges
Dr. Karmach

Worked example 1: solution

Cl–Cl (the bond inside Cl₂ gas)
electronegativity: Cl = 3.16 · Cl = 3.16
Step 1 · Find the electronegativity difference
ΔEN = 3.16 − 3.16 = 0
Step 2 · Place it on the continuum Step 3 · Name the bond and mark the charges
Cl–Cl → nonpolar covalent
equal electronegativities · the pair sits centered · no partial charges
Two atoms of the same element always pull equally. A bond between identical atoms is nonpolar, every time.
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Worked example 1: the bond on the continuum

Cl–Cl: ΔEN = 3.16 − 3.16 = 0
electronegativity: Cl = 3.16 · Cl = 3.16 · found: nonpolar covalent

Zero sits at the far left end of the continuum. Identical atoms share the pair evenly.
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Worked example 2: the H–Cl bond

H–Cl (hydrogen chloride)
electronegativity: H = 2.20 · Cl = 3.16 · wanted: bond type and partial charges

Hydrogen and chlorine share one pair of electrons.

A common first answer marks hydrogen as δ−. Test it against the two electronegativities.

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Worked example 2: solution

H–Cl (hydrogen chloride)
electronegativity: H = 2.20 · Cl = 3.16

Step 1 · Find the electronegativity difference

ΔEN = 3.16 − 2.20 = 0.96
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Worked example 2: solution

H–Cl (hydrogen chloride)
electronegativity: H = 2.20 · Cl = 3.16
Step 1 · Find the electronegativity difference
ΔEN = 3.16 − 2.20 = 0.96
Step 2 · Place it on the continuum

A difference of 0.96 sits between the 0.4 and 1.7 guidelines: polar covalent. The pair is shared, but not equally.

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Worked example 2: solution

H–Cl (hydrogen chloride)
electronegativity: H = 2.20 · Cl = 3.16
Step 1 · Find the electronegativity difference
ΔEN = 3.16 − 2.20 = 0.96
Step 2 · Place it on the continuum Step 3 · Name the bond and mark the charges
H–Cl → polar covalent, δ− on Cl
Cl (3.16) pulls harder than H (2.20) · the shared pair shifts toward Cl · H is δ+
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Worked example 2: solution

H–Cl (hydrogen chloride)
electronegativity: H = 2.20 · Cl = 3.16
Step 1 · Find the electronegativity difference
ΔEN = 3.16 − 2.20 = 0.96
Step 2 · Place it on the continuum Step 3 · Name the bond and mark the charges
H–Cl → polar covalent, δ− on Cl
Cl (3.16) pulls harder than H (2.20) · the shared pair shifts toward Cl · H is δ+
The partial negative marks the more electronegative atom, the one that pulls the pair closer. Marking hydrogen reversed the direction the electrons shift.
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Worked example 2: the bond on the continuum

H–Cl: ΔEN = 3.16 − 2.20 = 0.96
electronegativity: H = 2.20 · Cl = 3.16 · found: polar covalent, δ− on Cl

0.96 lands inside the middle band, between the 0.4 and 1.7 guidelines: unequal sharing.
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Take-home: δ− marks the stronger pull

H–Cl → δ− on Cl
Cl = 3.16 pulls harder than H = 2.20 · the shared pair shifts toward Cl
subtract backwards: 2.20 − 3.16 = −0.96
the negative sign points from δ+ toward δ−; it never puts the partial negative on H

The partial negative sits on the more electronegative atom. The size of the difference sets how polar the bond is; the direction of the pull sets which atom is δ−.

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Your turn: the Na–Cl bond

Na–Cl (sodium chloride)
electronegativity: Na = 0.93 · Cl = 3.16
ΔEN = 3.16 − 0.93 = →

Compute the difference, place it on the continuum, and name the bond.

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Your turn: the Na–Cl bond

Na–Cl (sodium chloride)
electronegativity: Na = 0.93 · Cl = 3.16
ΔEN = 3.16 − 0.93 = →

Compute the difference, place it on the continuum, and name the bond.

ΔEN = 3.16 − 0.93 = 2.23 → a large difference: ionic
Na–Cl → ionic
a metal and a nonmetal · Cl pulls the electron off Na completely · Na⁺ and Cl⁻
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Your turn: the bond on the continuum

Na–Cl: ΔEN = 3.16 − 0.93 = 2.23
electronegativity: Na = 0.93 · Cl = 3.16 · found: ionic

2.23 lands well past 1.7, and Na is a metal: the electron transfers.
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Ionic, covalent, or both

A compound's bonding follows from its parts. Metal with nonmetal: ionic. Nonmetals only: covalent. A polyatomic ion brings both: atoms inside the ion share electrons, and ionic attraction holds the whole ion to its partner.

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Where this goes wrong

Putting δ− on the wrong atom. Shared electrons shift toward the more electronegative atom. In H–Cl, Cl (3.16) pulls harder than H (2.20), so δ− sits on Cl. Reading the trend backwards flips the charge onto H; subtracting 2.20 − 3.16 = −0.96 and dropping the sign does the same.
Calling a real difference nonpolar. Equal sharing happens only when the electronegativities match, as in Cl–Cl. An N–H difference of 3.04 − 2.20 = 0.84 is not zero, so the sharing is unequal: polar covalent, not nonpolar.
Calling a moderate difference ionic. Two nonmetals with a difference near 1 still share the pair: polar covalent. Full transfer takes a large gap, usually a metal bonded to a nonmetal.
Reading the boundary as a wall. H–F has a difference of 1.78, past the 1.7 guideline, yet HF is a molecular gas that shares its pair: polar covalent. Two nonmetals share; the number guides, the metal-versus-nonmetal test decides at the edge.
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Practice 1: bonding in four compounds

NaF · SO₂ · FeSO₄ · Ca(ClO₂)₂
wanted: ionic, covalent, or both, for each compound in order

What bonding does each compound have, in order?

  1. ionic · covalent · both · both
  2. ionic · covalent · ionic · ionic
  3. ionic · covalent · both · ionic
  4. ionic · covalent · covalent · covalent
  5. ionic · ionic · both · both
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Practice 1 answer: A

NaF · SO₂ · FeSO₄ · Ca(ClO₂)₂
Na, Fe, Ca: metals · Fe²⁺ + SO₄²⁻ · Ca²⁺ + 2 ClO₂⁻ · SO₄²⁻ and ClO₂⁻: polyatomic ions
NaF → ionic · SO₂ → covalent · FeSO₄ → both · Ca(ClO₂)₂ → both → answer A

B stopped at the metal; S–O inside SO₄²⁻ and Cl–O inside ClO₂⁻ are shared pairs. C missed the chlorite ion: ClO₂⁻ is chlorate, ClO₃⁻, minus one oxygen, held together by shared Cl–O pairs. D kept only the bonds inside the ions; Fe²⁺ attracting SO₄²⁻ is ionic bonding. E read SO₂ as ions; S and O are both nonmetals, so they share: covalent only.

A metal with a polyatomic ion gives both: shared pairs inside the ion, ionic attraction between the ions.
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Practice 2: ionic, covalent, or both

CaCl₂ · NH₄NO₃ · P₂O₅ · CH₃OH
wanted: the compound with both ionic and covalent bonding

Which compound contains both ionic and covalent bonds?

  1. CaCl₂
  2. NH₄NO₃
  3. P₂O₅
  4. CH₃OH
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Practice 2 answer: B

CaCl₂ · NH₄NO₃ · P₂O₅ · CH₃OH
NH₄NO₃ = NH₄⁺ + NO₃⁻ → N–H and N–O shared inside each ion · NH₄⁺ attracts NO₃⁻ → both → answer B

A counted the two chlorines as bonded to each other; CaCl₂ is Ca²⁺ with two separate Cl⁻ ions, ionic only. C read the subscripts as a formula unit of ions; P and O are both nonmetals, so P₂O₅ shares: covalent only. D read the OH as hydroxide; CH₃OH has no ions at all, every atom a nonmetal sharing: covalent only.

No metal does not mean no ions. NH₄⁺ is a cation built of nonmetals, so any compound of it has covalent bonds inside the ion and ionic attraction between ions.
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Practice 3: the S–O bond

S–O (a sulfur–oxygen bond)
electronegativity: S = 2.58 · O = 3.44 · wanted: bond type and δ−

How is the S–O bond best classified?

  1. Nonpolar covalent, the two atoms share the pair equally
  2. Polar covalent, with S carrying the partial negative charge (δ−)
  3. Polar covalent, with O carrying the partial negative charge (δ−)
  4. Ionic, O pulls an electron completely away from S
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Practice 3 answer: C

S–O (a sulfur–oxygen bond)
electronegativity: S = 2.58 · O = 3.44
ΔEN = 3.44 − 2.58 = 0.86 → moderate: polar covalent, δ− on O → answer C

B put δ− on the wrong atom: O (3.44) pulls harder than S (2.58), so the pair shifts toward O; subtracting backwards, 2.58 − 3.44 = −0.86, only flips the sign, not the direction. A ignored the difference: 0.86 is not zero, so the sharing is unequal, not nonpolar. D read sharing as transfer: two nonmetals 0.86 apart still share the pair, polar covalent, not ionic.

A moderate difference means unequal sharing, and the pair sits closer to the more electronegative atom. O is δ−, S is δ+.
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Worked example 3: the H–F bond

H–F (hydrogen fluoride)
electronegativity: H = 2.20 · F = 3.98 · wanted: bond type

Hydrogen fluoride is a gas that dissolves in water to make an acid.

A common first answer: the difference clears 1.7, so call the bond ionic. Test it.

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Worked example 3: solution

H–F (hydrogen fluoride)
electronegativity: H = 2.20 · F = 3.98

Step 1 · Find the electronegativity difference

ΔEN = 3.98 − 2.20 = 1.78
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Worked example 3: solution

H–F (hydrogen fluoride)
electronegativity: H = 2.20 · F = 3.98
Step 1 · Find the electronegativity difference
ΔEN = 3.98 − 2.20 = 1.78
Step 2 · Place it on the continuum

1.78 sits just past the 1.7 guideline. The boundary is not a wall: H and F are both nonmetals, and two nonmetals share.

Dr. Karmach

Worked example 3: solution

H–F (hydrogen fluoride)
electronegativity: H = 2.20 · F = 3.98
Step 1 · Find the electronegativity difference
ΔEN = 3.98 − 2.20 = 1.78
Step 2 · Place it on the continuum Step 3 · Name the bond and mark the charges
H–F → polar covalent, δ− on F
two nonmetals · the pair stays shared but pulled far toward F · H is δ+
Dr. Karmach

Worked example 3: solution

H–F (hydrogen fluoride)
electronegativity: H = 2.20 · F = 3.98
Step 1 · Find the electronegativity difference
ΔEN = 3.98 − 2.20 = 1.78
Step 2 · Place it on the continuum Step 3 · Name the bond and mark the charges
H–F → polar covalent, δ− on F
two nonmetals · the pair stays shared but pulled far toward F · H is δ+
HF is a molecular gas, not a lattice of ions. The most lopsided sharing among the common bonds is still sharing, not transfer.
Dr. Karmach

Worked example 3: the bond on the continuum

H–F: ΔEN = 3.98 − 2.20 = 1.78
electronegativity: H = 2.20 · F = 3.98 · found: polar covalent, δ− on F

Just past the 1.7 guideline, yet H and F are both nonmetals: the pair stays shared, polar covalent.
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Practice 4: the most polar bond

B–F · Si–Cl · O–F
electronegativity: B = 2.04 · F = 3.98 · Si = 1.90 · Cl = 3.16 · O = 3.44 · wanted: the most polar bond and its δ− atom

Which of these bonds is the most polar, and which atom in it carries the partial negative charge?

  1. Si–Cl, with Cl carrying δ−
  2. O–F, with F carrying δ−
  3. B–F, with B carrying δ−
  4. B–F, with F carrying δ−
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Practice 4 answer: D

B–F · Si–Cl · O–F
electronegativity: B = 2.04 · F = 3.98 · Si = 1.90 · Cl = 3.16 · O = 3.44
B–F: 3.98 − 2.04 = 1.94 · Si–Cl: 3.16 − 1.90 = 1.26 · O–F: 3.98 − 3.44 = 0.54 → B–F, δ− on F → answer D

A dropped B–F because 1.94 clears 1.7 and settled for Si–Cl at 1.26; a bigger difference only makes a bond more polar, and with no metal in it B–F still shares its pair. B picked the two most electronegative atoms; polarity comes from the difference, and 3.98 − 3.44 = 0.54 is the smallest of the three. C put δ− on the wrong atom: F (3.98) pulls harder than B (2.04); 2.04 − 3.98 = −1.94 flips only the sign.

The biggest difference makes the most polar bond, and 1.7 is a guideline, not a wall: with no metal in the bond, a big difference is still sharing. F is δ−.
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Practice 5: four bonds to fluorine

Li–F · H–F · N–F · F–F
electronegativity: Li = 0.98 · H = 2.20 · N = 3.04 · F = 3.98 · wanted: each bond's type, in order

What type is each bond, in order?

  1. ionic · ionic · ionic · nonpolar covalent
  2. ionic · polar covalent · nonpolar covalent · nonpolar covalent
  3. ionic · polar covalent · polar covalent · polar covalent
  4. ionic · polar covalent · polar covalent · nonpolar covalent
  5. ionic · ionic · polar covalent · nonpolar covalent
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Practice 5 answer: D

Li–F · H–F · N–F · F–F
electronegativity: Li = 0.98 · H = 2.20 · N = 3.04 · F = 3.98
Li–F: 3.00 · H–F: 1.78 · N–F: 0.94 · F–F: 0 → ionic · polar covalent · polar covalent · nonpolar covalent → answer D

A called every large difference ionic: H–F (1.78) and N–F (0.94) join two nonmetals, which share. B called a real difference nonpolar: 0.94 is not zero. C took fluorine's own high electronegativity for polarity; in F–F, 3.98 − 3.98 = 0. E read the 1.7 boundary as a wall: H–F is two nonmetals sharing a pair, polar covalent.

Only the difference counts, and at the edge the metal test decides. Li–F is the one metal–nonmetal pair. ✓
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Practice 6: the Cl–F bond

Cl–F (chlorine monofluoride, ClF)
electronegativity: Cl = 3.16 · F = 3.98 · wanted: bond type and δ−

Which description fits the Cl–F bond?

  1. Nonpolar covalent: Cl and F sit in the same group, so they pull equally
  2. Polar covalent, with F carrying the partial negative charge (δ−)
  3. Polar covalent, with Cl carrying the partial negative charge (δ−)
  4. Ionic, F pulls an electron completely away from Cl
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Practice 6 answer: B

Cl–F (chlorine monofluoride, ClF)
electronegativity: Cl = 3.16 · F = 3.98
ΔEN = 3.98 − 3.16 = 0.82 → moderate: polar covalent, δ− on F → answer B

A read the shared group as an equal pull: electronegativity climbs up a group, and 0.82 is not zero, so the sharing is unequal. C gave δ− to the larger atom: Cl holds more electrons, but F (3.98) pulls the shared pair harder than Cl (3.16); 3.16 − 3.98 = −0.82 flips only the sign. D read sharing as transfer: two nonmetals 0.82 apart share the pair.

Same group does not mean same pull. F sits above Cl and pulls harder: F is δ−, Cl is δ+.
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Practice 7: the K–I and P–F bonds

K–I · P–F
electronegativity: K = 0.82 · I = 2.66 · P = 2.19 · F = 3.98 · wanted: each bond's type and δ−

How is each bond classified?

  1. K–I ionic · P–F ionic
  2. K–I polar covalent (δ− on I) · P–F polar covalent (δ− on F)
  3. K–I ionic · P–F polar covalent (δ− on F)
  4. K–I ionic · P–F polar covalent (δ− on P)
  5. K–I polar covalent (δ− on I) · P–F ionic
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Practice 7 answer: C

K–I · P–F
electronegativity: K = 0.82 · I = 2.66 · P = 2.19 · F = 3.98 · K: a metal · P, I, F: nonmetals
K–I: ΔEN = 2.66 − 0.82 = 1.84 → metal + nonmetal: ionic, K⁺ and I⁻
P–F: ΔEN = 3.98 − 2.19 = 1.79 → two nonmetals: polar covalent, δ− on F → answer C

A read 1.7 as a wall: P and F are nonmetals, so they share the pair. B ignored the metal: K gives its electron to I. D put δ− on the wrong atom: F (3.98) outpulls P (2.19); 2.19 − 3.98 = −1.79 flips only the sign. E judged by the strongest atom: the difference and the metal test set the type, not F alone.

Differences 0.05 apart, two bond types. Near 1.7 the metal test decides: K–I forms ions, P–F shares.
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Check yourself

  1. A C–O bond has electronegativities C = 2.55 and O = 3.44. Find the difference, classify the bond, and mark the atom that carries δ−.
  2. Two atoms form a bond with a difference of 0. What kind of bond is it, and where do the partial charges sit?
  3. Is the bonding in K₂SO₄ ionic, covalent, or both? Name which bonds are which.

A bond type tells you how one shared pair of electrons is held. A whole molecule is built from several bonds arranged in space, and drawing that arrangement is the next step: Lewis structures.

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2 · Lewis Structures

Count a molecule's valence electrons and draw its Lewis structure, placing every electron as a bond or a lone pair.

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Parts with a fixed number of connectors

A model kit builds molecules. Each part has connectors: H one, O two, N three, C four. HONC 1-2-3-4. You build only what they allow.

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Every valence electron is accounted for

A molecule owns a fixed pool of valence electrons. A Lewis structure places every one of them as bonds or lone pairs. None is invented; none is lost.

H₂O: 8 valence electrons = 4 in bonds + 4 in lone pairs
2 O–H bonds (4) · 2 lone pairs on O (4) · every electron accounted for ✓
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Valence electrons come from the group number

Only the outermost electrons, the valence electrons, form bonds. For a main-group atom their count is the ones digit of the group number.

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The Lewis symbol: valence electrons as dots

A Lewis symbol writes the element with one dot per valence electron. Dots sit singly on the four sides first, then pair. Eight dots is a full shell.

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Ions in Lewis symbols

A metal atom empties its valence shell to form a cation: the dots leave with the electrons. A nonmetal gains electrons until eight dots surround it: an anion. Brackets around the symbol, charge outside.

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Your turn: the magnesium dot symbol

Mg: group 2 → 2 valence electrons
12 electrons in the atom · 10 core stay hidden · 2 valence become dots

Fill the blanks, then write the symbol.

step count
dots around Mg
paired or single
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Your turn: the magnesium dot symbol

Mg: group 2 → 2 valence electrons
12 electrons in the atom · 10 core stay hidden · 2 valence become dots

Fill the blanks, then write the symbol.

step count
dots around Mg
paired or single
·Mg·  ·  2 dots, single, on two different sides
dots sit singly on the four sides first · pairing starts only at the fifth dot
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Practice 1: the dot symbol for phosphorus

P: group 15 → 5 valence electrons
the ones digit of the group number · dots sit singly on the four sides first, then pair

Which dot symbol is correct for a phosphorus atom?

  1. P with 5 dots: one pair and three single dots
  2. P with 3 dots: one on each of three sides
  3. P with 15 dots surrounding the symbol
  4. P with 5 dots: two pairs and one single dot
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Practice 1 answer: A

P: group 15 → ones digit 5 → 5 dots → answer A
four dots fill the four sides singly · the fifth makes one pair · one pair + three single dots

B counted the period: P sits in period 3, but dots come from the group, 15 → 5. C drew the whole group number as 15 dots; only the 5 valence electrons appear. D paired too early: dots fill all four sides singly before any pair forms, so 5 dots make one pair, not two.

The three single dots mark where phosphorus bonds: three bonds and one lone pair, exactly the NF₃ pattern.
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Practice 2: the dot symbol for the sulfide ion

S²⁻: 6 + 2 = 8 electrons shown as dots
S is group 16 → 6 valence electrons · the 2− charge adds 2 more

Which drawing shows the sulfide ion correctly?

  1. [S with 8 dots]²⁻: brackets around the symbol, charge outside
  2. S with 8 dots, no brackets and no charge
  3. [S with 6 dots]²⁻: the six dots sulfur started with
  4. [S with 4 dots]²⁺: two dots removed, a positive charge
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Practice 2 answer: A

S²⁻: 6 + 2 = 8 dots · brackets, 2− outside → answer A
a nonmetal gains electrons until eight dots surround it

B drew the dots but dropped the brackets and charge; eight dots on a plain S claims a neutral atom, and neutral sulfur has 6. C pasted the charge onto the original 6 dots; the 2− exists because 2 electrons arrived, so 6 + 2 = 8 dots must show. D ran the transfer backwards: 6 − 2 = 4 dots with 2+ describes a cation, and nonmetals gain.

Charge and dot count move together: 2− means 2 extra dots, and the brackets say the whole package carries the charge.
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Ionic bonds form by electron transfer

A metal atom gives its valence electrons to a nonmetal atom. Both ions end with a filled shell. The opposite charges attract, and that attraction holds the ions together as an ionic bond.

Na loses 1 e⁻ · Cl gains 1 e⁻ → NaCl
1 e⁻ lost = 1 e⁻ gained ✓ · charges: (+1) + (−1) = 0 ✓
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Electrons lost equal electrons gained

Magnesium has two valence electrons to give. Each bromine needs only one to reach eight. Two bromine atoms take the pair, so the formula is MgBr₂. Balancing the electrons balances the charges.

Mg loses 2 e⁻ · each Br gains 1 e⁻ → 1 Mg : 2 Br → MgBr₂
2 e⁻ lost = 2 × 1 e⁻ gained ✓ · charges: (+2) + 2(−1) = 0 ✓
Dr. Karmach

Your turn: lithium and oxygen

Li: group 1 · O: group 16
the metal gives electrons · the nonmetal takes them until it holds eight

Draw both Lewis symbols, arrow the transferred electrons, then fill the blanks and write the formula.

step count
electrons each Li loses
electrons one O gains
Li atoms needed per O
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Your turn: lithium and oxygen

Li: group 1 · O: group 16
the metal gives electrons · the nonmetal takes them until it holds eight

Draw both Lewis symbols, arrow the transferred electrons, then fill the blanks and write the formula.

step count
electrons each Li loses
electrons one O gains
Li atoms needed per O
Li·  Li·  +  O with 6 dots → 2 Li⁺ + [O with 8 dots]²⁻ → Li₂O
each Li loses 1 · O gains 2 · 2 Li per O · charges: 2(+1) + (−2) = 0 ✓
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Practice 3: aluminum and sulfur

aluminum + sulfur → an ionic compound
Al: group 13 · S: group 16

What is the formula of the ionic compound that aluminum and sulfur form?

  1. AlS
  2. Al₂S₃
  3. Al₃S₂
  4. Al₆S₃
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Practice 3 answer: B

each Al loses 3 e⁻ · each S gains 2 e⁻ · 2 × 3 = 3 × 2 = 6 → Al₂S₃ → answer B
6 e⁻ lost = 6 e⁻ gained ✓ · charges: 2(+3) + 3(−2) = 0 ✓

A paired one Al with one S without counting electrons: 3 lost against 2 gained. C wrote each element's own electron count as its own subscript: Al₃S₂ has 3 × 3 = 9 lost against 2 × 2 = 4 gained. D crossed the dot counts, 3 and 6, instead of the electrons that move: Al₆S₃ has 6 × 3 = 18 lost against 3 × 2 = 6 gained.

Neither 3 nor 2 divides the other, so both subscripts exceed 1. The electrons balance at 6, the smallest number both 3 and 2 divide into.
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The electron pool

Add every atom's valence electrons. For an ion, adjust: add one electron per negative charge, subtract one per positive.

CO₂: 4 + 2(6) = 16
1 C (group 14 → 4) · 2 O (group 16 → 6) · neutral, no adjustment
OH⁻: 6 + 1 + 1 = 8  ·  NH₄⁺: 5 + 4(1) − 1 = 8
OH⁻ adds 1 for the 1− charge · NH₄⁺ subtracts 1 for the 1+ charge
Dr. Karmach

Bonds, lone pairs, and the octet

A shared pair drawn as a line is a bond: one pair single, two double, three triple. Each main-group atom aims for eight electrons, an octet. Hydrogen aims for two, a duet.

Dr. Karmach

The method

  1. Count the valence electrons.
  2. Draw the skeleton: least electronegative atom centered, never H; single bonds.
  3. Complete the outer octets: lone pairs; H a duet.
  4. Place leftovers on the center.
  5. Form multiple bonds if the center lacks an octet.
Dr. Karmach

Worked example 1: water

Step 1 · Count the valence electrons

H₂O: 2(1) + 6 = 8
2 H (group 1 → 1) · 1 O (group 16 → 6) · 8 valence electrons to place

Oxygen is less electronegative than hydrogen, and H is never central. Draw the Lewis structure.

Dr. Karmach

Worked example 1: solution

H₂O: 2(1) + 6 = 8
8 valence electrons to place

Step 2 · Draw the skeleton

Oxygen in the center, one single bond to each H.

H–O–H
2 single bonds use 2 × 2 = 4 electrons · 4 of 8 placed
Dr. Karmach

Worked example 1: solution

H₂O: 2(1) + 6 = 8
8 valence electrons to place
Step 2 · Draw the skeleton
H–O–H
2 single bonds use 2 × 2 = 4 electrons · 4 of 8 placed
Step 3 · Complete the outer octets

The outer atoms are hydrogen; a single bond already fills each H's duet.

Dr. Karmach

Worked example 1: solution

H₂O: 2(1) + 6 = 8
8 valence electrons to place
Step 2 · Draw the skeleton
H–O–H
2 single bonds use 2 × 2 = 4 electrons · 4 of 8 placed
Step 3 · Complete the outer octets

The outer atoms are hydrogen; a single bond already fills each H's duet.

Four electrons fill the two O–H bonds and each hydrogen has its duet. Four remain for oxygen.
Dr. Karmach

Worked example 1: the oxygen lone pairs

Four electrons sit in the two O–H bonds; the outer hydrogens are done. Four remain.

Step 4 · Place leftovers on the center

8 − 4 = 4 electrons left → 2 lone pairs on O
O: 2 bonds (4) + 2 lone pairs (4) = 8 → octet ✓

Dr. Karmach

Worked example 1: the oxygen lone pairs

Four electrons sit in the two O–H bonds; the outer hydrogens are done. Four remain.

Step 4 · Place leftovers on the center

8 − 4 = 4 electrons left → 2 lone pairs on O
O: 2 bonds (4) + 2 lone pairs (4) = 8 → octet ✓

All 8 valence electrons placed: 4 in bonds, 4 in lone pairs. O has an octet; each H a duet.
Dr. Karmach

Worked example 1: the electron budget

H₂O: 8 valence electrons = 4 in bonds + 4 in lone pairs on O
steps 1 to 4 used · step 5 not needed

The pool is used up at step 4 and oxygen has its octet, so step 5 never runs. ✓
Dr. Karmach

Worked example 2: nitrogen trifluoride

Step 1 · Count the valence electrons

NF₃
given: 1 nitrogen, 3 fluorine · wanted: the electron pool, then the structure

A common first attempt counts one group number per element. Find the pool, then draw the structure.

Dr. Karmach

Worked example 2: solution

Step 1 · Count the valence electrons

NF₃: 5 + 3(7) = 26  ·  one-per-element 5 + 7 = 12 ✗
each F brings its own 7: multiply by the subscript · 26 to place
Dr. Karmach

Worked example 2: solution

Step 1 · Count the valence electrons

NF₃: 5 + 3(7) = 26  ·  one-per-element 5 + 7 = 12 ✗
each F brings its own 7: multiply by the subscript · 26 to place
Step 2 · Draw the skeleton

Nitrogen is least electronegative, so it takes the center, with a single bond to each F.

3 N–F single bonds: 3 × 2 = 6 electrons
6 of 26 placed

Dr. Karmach

Worked example 2: solution

Step 1 · Count the valence electrons

NF₃: 5 + 3(7) = 26  ·  one-per-element 5 + 7 = 12 ✗
each F brings its own 7: multiply by the subscript · 26 to place
Step 2 · Draw the skeleton

Nitrogen is least electronegative, so it takes the center, with a single bond to each F.

3 N–F single bonds: 3 × 2 = 6 electrons
6 of 26 placed

Six of the 26 electrons fill the three N–F bonds. Twenty remain for the fluorine octets and the center.
Dr. Karmach

Worked example 2: the fluorine octets

Six electrons sit in the three N–F bonds. Each fluorine still needs three lone pairs.

Step 3 · Complete the outer octets

each F: 3 lone pairs → 3 × 6 = 18 electrons
6 + 18 = 24 of 26 placed · every F has its octet

Dr. Karmach

Worked example 2: the fluorine octets

Six electrons sit in the three N–F bonds. Each fluorine still needs three lone pairs.

Step 3 · Complete the outer octets

each F: 3 lone pairs → 3 × 6 = 18 electrons
6 + 18 = 24 of 26 placed · every F has its octet

Twenty-four of the 26 electrons are placed and every fluorine has its octet. Two remain for the center.
Dr. Karmach

Worked example 2: the nitrogen lone pair

Six electrons sit in the three N–F bonds and eighteen fill the fluorine octets. Two remain.

Step 4 · Place leftovers on the center

26 − 6 − 18 = 2 → 1 lone pair on N
N: 3 bonds (6) + 1 lone pair (2) = 8 → octet ✓

Dr. Karmach

Worked example 2: the nitrogen lone pair

Six electrons sit in the three N–F bonds and eighteen fill the fluorine octets. Two remain.

Step 4 · Place leftovers on the center

26 − 6 − 18 = 2 → 1 lone pair on N
N: 3 bonds (6) + 1 lone pair (2) = 8 → octet ✓

All 26 valence electrons placed; every F and the N reaches an octet. One per element stops at 12 and leaves the structure short.
Dr. Karmach

Worked example 2: the electron budget

NF₃: 26 valence electrons = 6 in bonds + 18 on the F atoms + 2 on N
steps 1 to 4 used · step 5 not needed

The same four steps as water. The outer octets take the largest share: 18 of 26. ✓
Dr. Karmach

Take-home: count every atom, not every element

NF₃: 5 + 3(7) = 26 ✓  ·  5 + 7 = 12 ✗
three fluorine atoms bring 3 × 7 = 21 electrons, not 7

Each atom brings its own valence electrons. Multiply each element's group number by its subscript in the formula, then add.

Dr. Karmach

Your turn: methane, CH₄

CH₄: 4 + 4(1) = 8
1 C (group 14 → 4) · 4 H (group 1 → 1) · 8 valence electrons

Carbon is the central atom. Fill the blanks.

step count
electrons in the 4 C–H bonds
electrons left for lone pairs
Dr. Karmach

Your turn: methane, CH₄

CH₄: 4 + 4(1) = 8
1 C (group 14 → 4) · 4 H (group 1 → 1) · 8 valence electrons

Carbon is the central atom. Fill the blanks.

step count
electrons in the 4 C–H bonds
electrons left for lone pairs
4 C–H bonds: 4 × 2 = 8  ·  leftover 8 − 8 = 0
C: 4 bonds (8) = octet ✓ · every H a duet · no lone pairs

Dr. Karmach

Where this goes wrong

Counting each element once. For NF₃, adding one group number per element gives 5 + 7 = 12. Every atom brings its own: 5 + 3(7) = 26. Multiply each group number by its subscript.
Counting all the electrons. CO₂ holds 6 + 2(8) = 22 electrons in total, but only the valence electrons are drawn: 4 + 2(6) = 16. Core electrons stay out of the structure.
Ignoring the ion's charge. NH₄⁺ carries a 1+ charge, so subtract one electron: 5 + 4(1) − 1 = 8, not 9. A negative ion adds electrons; a positive ion removes them.
Leaving the center short. With only single bonds, the carbon in CO₂ has 4 electrons, not 8. When the center lacks an octet, form double or triple bonds.
Dr. Karmach

Practice 4: oxygen difluoride

OF₂
fluorine is the most electronegative atom, so oxygen is the central atom

How many valence electrons must appear in the Lewis structure of OF₂?

  1. 18
  2. 13
  3. 26
  4. 20
Dr. Karmach

Practice 4 answer: D

OF₂: 6 + 2(7) = 20 → answer D
1 O (group 16 → 6) · 2 F (group 17 → 7) · neutral, no adjustment

B counted each element once: 6 + 7 = 13. C counted every electron, core included: 8 + 2(9) = 26. A dropped a pair: 20 − 2 = 18.

20 valence electrons place as 2 O–F bonds (4) and 8 lone pairs (16): 4 + 16 = 20, every atom an octet.

Dr. Karmach

Practice 5: the structure of CH₂Br₂

CH₂Br₂
wanted: the correct Lewis structure

Which drawing is the correct Lewis structure of CH₂Br₂?

  1. one lone pair on each Br
  2. three lone pairs on each Br and on each H
  3. three lone pairs on each Br, one on C
  4. three lone pairs on each Br, none on C or H
Dr. Karmach

Practice 5 answer: D

CH₂Br₂: 4 + 2(1) + 2(7) = 20 → answer D
4 bonds (8) + 3 lone pairs on each Br (12) · 20 − 8 − 12 = 0 left for C · C 8 ✓ · each Br 8 ✓ · each H a duet ✓

A counted each element once: 4 + 1 + 7 = 12, leaving 12 − 8 = 4 after the bonds, one pair per Br. B gave hydrogen an octet: 8 + 12 + 12 = 32 drawn from a pool of 20; H takes a duet. C put a lone pair on carbon with none left: 8 + 12 + 2 = 22, and carbon holds 10.

Carbon's four bonds already give it eight. With nothing left over, the center carries no lone pair, as in CH₄.
Dr. Karmach

Worked example 3: carbon dioxide

Step 1 · Count the valence electrons

CO₂: 4 + 2(6) = 16
1 C (group 14 → 4) · 2 O (group 16 → 6) · 16 valence electrons to place

Carbon is least electronegative, so it takes the center. Draw the Lewis structure.

Dr. Karmach

Worked example 3: solution

Step 2 · Draw the skeleton

Carbon centered, a single bond to each oxygen.

O–C–O: 2 single bonds use 2 × 2 = 4 electrons
4 of 16 placed

Dr. Karmach

Worked example 3: solution

Step 2 · Draw the skeleton

Carbon centered, a single bond to each oxygen.

O–C–O: 2 single bonds use 2 × 2 = 4 electrons
4 of 16 placed

Four of the 16 electrons fill the two C–O bonds. Twelve remain for the outer octets.
Dr. Karmach

Worked example 3: the outer octets

Step 3 · Complete the outer octets

each O gets 3 lone pairs: 2 × 6 = 12 electrons
4 + 12 = 16: all placed, but carbon has only 4 (no octet)

Dr. Karmach

Worked example 3: the outer octets

Step 3 · Complete the outer octets

each O gets 3 lone pairs: 2 × 6 = 12 electrons
4 + 12 = 16: all placed, but carbon has only 4 (no octet)


Step 4 · Place leftovers on the center

None remain: 16 − 4 − 12 = 0. The carbon is still two pairs short of an octet.

Dr. Karmach

Worked example 3: the outer octets

Step 3 · Complete the outer octets

each O gets 3 lone pairs: 2 × 6 = 12 electrons
4 + 12 = 16: all placed, but carbon has only 4 (no octet)


Step 4 · Place leftovers on the center

None remain: 16 − 4 − 12 = 0. The carbon is still two pairs short of an octet.

Every electron is placed, yet carbon holds only 4. Single bonds cannot finish this structure.
Dr. Karmach

Worked example 3: two double bonds

Carbon sits two pairs short of an octet. Pull one lone pair from each oxygen into a bond.

Step 5 · Form multiple bonds

O=C=O
C: 2 double bonds (8) = octet ✓ · each O: 1 double bond (4) + 2 lone pairs (4) = 8 ✓

Dr. Karmach

Worked example 3: two double bonds

Carbon sits two pairs short of an octet. Pull one lone pair from each oxygen into a bond.

Step 5 · Form multiple bonds

O=C=O
C: 2 double bonds (8) = octet ✓ · each O: 1 double bond (4) + 2 lone pairs (4) = 8 ✓

All 16 valence electrons placed. Single bonds could not give carbon an octet; two double bonds can.
Dr. Karmach

Worked example 3: the electron budget

CO₂: 16 valence electrons = 8 in bonds + 8 in lone pairs on O
all five steps used · step 4 adds nothing: none left

The pool ran out with carbon at 4. Step 5 moves 2 lone pairs into bonds: 4 + 4 = 8 in bonds. No electron is added. ✓
Dr. Karmach

Resonance: two correct drawings of ozone

Ozone's 18 valence electrons need one O=O double bond, and it fits on either side. Both drawings are correct. The measured bonds are identical: the real molecule, the resonance hybrid, blends the two.

O₃: 3(6) = 18 · O=O–O ↔ O–O=O
measured: both O–O bonds the same length, between a single and a double bond
Dr. Karmach

Worked example 4: the carbonate ion

Step 1 · Count the valence electrons

CO₃²⁻: 4 + 3(6) + 2 = 24
1 C (group 14 → 4) · 3 O (group 16 → 6) · the 2− charge adds 2 · 24 to place

Carbon takes the center. Draw the Lewis structure, then count its equivalent drawings.

Dr. Karmach

Worked example 4: solution

Step 2 · Draw the skeleton Step 3 · Complete the outer octets Step 4 · Place leftovers on the center

Carbon centered, a single bond to each of the three oxygens; each oxygen then takes three lone pairs.

3 C–O bonds (6) + 3 lone pairs on each O (18) = 24 · 24 − 6 − 18 = 0 left
all 24 placed · carbon holds only 6, one pair short of an octet
Dr. Karmach

Worked example 4: solution

Step 2 · Draw the skeleton Step 3 · Complete the outer octets Step 4 · Place leftovers on the center

3 C–O bonds (6) + 3 lone pairs on each O (18) = 24 · 24 − 6 − 18 = 0 left
all 24 placed · carbon holds only 6, one pair short of an octet
Step 5 · Form multiple bonds

Dr. Karmach

Worked example 4: solution

Step 2 · Draw the skeleton Step 3 · Complete the outer octets Step 4 · Place leftovers on the center

3 C–O bonds (6) + 3 lone pairs on each O (18) = 24 · 24 − 6 − 18 = 0 left
all 24 placed · carbon holds only 6, one pair short of an octet
Step 5 · Form multiple bonds

Any of the three O atoms can hold the C=O: three equivalent drawings. The real ion has three identical C–O bonds, between single and double.
Dr. Karmach

Worked example 4: the electron budget

CO₃²⁻: 24 valence electrons = 8 in bonds + 16 in lone pairs on O
all five steps used · step 4 adds nothing: none left

The same route as CO₂, but only 1 lone pair moves: 6 + 2 = 8 in bonds. It can come from any of the 3 O atoms. ✓
Dr. Karmach

When resonance appears

Resonance appears when a multiple bond can sit in more than one place and every atom keeps its octet. Only bonds and lone pairs shift; atoms never move. The drawings are usually equivalent, but need not be.

CO₃²⁻, NO₃⁻: 3 structures · O₃, NO₂⁻: 2 structures · H₂O, C₂H₄: 1 structure
equivalent drawings in each · H₂O has no multiple bond · the C=C in C₂H₄ has one place
SCN⁻: S=C=N ↔ S≡C–N ↔ S–C≡N: 3 structures, not alike
16 valence electrons · every atom has an octet in all three · the bonds shift between different atoms
Dr. Karmach

Practice 6: hydrogen cyanide

HCN
skeleton H–C–N

In the Lewis structure of HCN, how many electrons sit in lone pairs?

  1. 10
  2. 2
  3. 6
  4. 8
  5. 4
Dr. Karmach

Practice 6 answer: B

HCN: 1 + 4 + 5 = 10 · H–C≡N: 1 single bond (2) + 1 triple bond (6) = 8 shared · 10 − 8 = 2 in lone pairs → answer B
C: single (2) + triple (6) = 8 ✓ · N: triple (6) + 1 lone pair (2) = 8 ✓ · H: duet ✓

A reported the whole pool of 10, not the lone-pair share. D counted the shared electrons, 2 + 6 = 8, instead of the ones left over. C stopped at single bonds: 10 − 4 = 6 in lone pairs, which leaves carbon with only 4 electrons. E stopped at a double bond: 2 + 4 = 6 shared, 10 − 6 = 4 in lone pairs, which leaves carbon with only 6.

Two of nitrogen's pairs move into the bond so carbon reaches eight. One lone pair, 2 electrons, is all that stays outside a bond.
Dr. Karmach

Practice 7: an octet check on N₂O

N₂O
skeleton N–N–O · lone pairs placed to use the valence electrons

Which drawing of N₂O breaks the octet rule?

  1. N=N=O
  2. N≡N–O
  3. N≡N=O
  4. N–N≡O
  5. none: all four are valid
Dr. Karmach

Practice 7 answer: C

N₂O: 2(5) + 6 = 16 · N≡N=O: 5 bond pairs = 10 shared · 16 − 10 = 6 in lone pairs → answer C
center N: triple (6) + double (4) = 10, past an octet ✗ · the other three: every atom 8 ✓

A counted two double bonds as too many: the center N has 4 + 4 = 8. B took the single-bonded O as unfinished: 2 + 6 = 8 with three lone pairs. D took O's triple bond as too many: 6 + 2 = 8 with one lone pair. E stopped before the center atom, where N≡N=O puts 10.

Count the center atom first: a triple and a double bond on one atom already make 10. The three valid drawings are the resonance structures of N₂O. ✓
Dr. Karmach

Practice 8: hydrogen peroxide

H₂O₂
skeleton H–O–O–H

How many lone pairs does the finished Lewis structure of hydrogen peroxide carry?

  1. 4
  2. 8
  3. 10
  4. 7
Dr. Karmach

Practice 8 answer: A

H₂O₂: 2(1) + 2(6) = 14 · 3 bonds: 3 × 2 = 6 · 14 − 6 = 8 → 4 lone pairs → answer A
each O: 2 bonds (4) + 2 lone pairs (4) = 8 ✓ · each H: a duet ✓ · no multiple bond needed

B counted the lone-pair electrons, 4 × 2 = 8, not the pairs. C gave each H an octet: 4 lone pairs on the O atoms plus 3 on each H makes 10, which needs 6 + 20 = 26 electrons from a pool of 14. D counted every pair in the pool as a lone pair: 14 ÷ 2 = 7, the 3 bonding pairs included.

Each oxygen carries two bonds and two lone pairs, as in water. The O–O bond takes the place of one O–H bond.
Dr. Karmach

Practice 9: urea

CO(NH₂)₂ (urea)
skeleton: C bonded to O and to both N · each N bonded to 2 H

Urea is the most widely used nitrogen fertilizer. In its correct Lewis structure, how many single bonds are there, and how many lone pairs?

  1. single bonds 7 · lone pairs 5
  2. single bonds 8 · lone pairs 4
  3. single bonds 6 · lone pairs 8
  4. single bonds 6 · lone pairs 4
  5. single bonds 2 · lone pairs 4
Dr. Karmach

Practice 9 answer: D

CO(NH₂)₂: 4 + 6 + 2(5) + 4(1) = 24 · 7 single bonds use 7 × 2 = 14 · 24 − 14 = 10
3 lone pairs on O (6) + 1 on each N (4) = 10 · C holds only 3 × 2 = 6 · one O lone pair moves into C=O
6 single bonds + 1 C=O · lone pairs: 2 on O + 1 on each N = 4 → answer D
bonds 6(2) + 4 = 16 · lone pairs 4 × 2 = 8 · 16 + 8 = 24 ✓ · C 8 ✓ · O 8 ✓ · each N 8 ✓ · each H a duet ✓

A stopped at step 4: 7 single bonds and 5 lone pairs place all 24 electrons, but carbon holds 6. B counted each line of C=O as a single bond: 6 + 2 = 8. C counted lone-pair electrons, 4 × 2 = 8, not pairs. E left out the four N–H bonds: 6 − 4 = 2.

A double bond is one bond, not two single bonds. Every bond to H is a single bond and counts.
Dr. Karmach

Practice 10: nitrosyl chloride

NOCl
electronegativity: N = 3.04 · Cl = 3.16 · O = 3.44 · wanted: the correct Lewis structure

Which is the correct Lewis structure of NOCl?

  1. O–N–Cl: 3 lone pairs on O, 1 on N, 3 on Cl
  2. O=N–Cl: 2 lone pairs on O, 1 on N, 3 on Cl
  3. N=O–Cl: 2 lone pairs on N, 1 on O, 3 on Cl
  4. O=N–Cl: 2 lone pairs on O, none on N, 3 on Cl
Dr. Karmach

Practice 10 answer: B

NOCl: 5 + 6 + 7 = 18 · N in the center · O–N–Cl uses 2 × 2 = 4
N 3.04 < Cl 3.16 < O 3.44 · 3 lone pairs each on O, Cl: 2 × 6 = 12 · 18 − 4 − 12 = 2 → 1 lone pair on N
N holds 2 + 2 + 2 = 6 → one O lone pair moves into N=O → O=N–Cl → answer B
bonds 2 + 4 = 6 · lone pairs 4 (O) + 2 (N) + 6 (Cl) = 12 · 6 + 12 = 18 ✓ · N 8 ✓ · O 8 ✓ · Cl 8 ✓

A stopped at step 4: all 18 electrons are placed, but N holds 2 + 2 + 2 = 6. C put O in the center because it sits in the middle of the formula; O has the highest electronegativity, so it belongs outside. D dropped the 2 leftover electrons: 18 − 2 = 16 drawn, and N holds 6.

Every atom in C also has an octet, so octets alone cannot pick the skeleton. Electronegativity does: the lowest value takes the center.
Dr. Karmach

Check yourself

  1. Count the valence electrons in NH₃, and name the central atom.
  2. In CO₂, why do single bonds fail and double bonds succeed?

The octet rule builds most structures, not all: boron can settle at six electrons, and heavier central atoms can hold more than eight.

Dr. Karmach

3 · Exceptions to the Octet Rule

Recognize and draw the three exception families: incomplete octets, odd-electron molecules, and expanded octets on period-3-or-lower central atoms.

Dr. Karmach

Three ways real molecules break the octet rule

The octet rule builds most structures, not all. Boron trifluoride stops at six electrons. Nitrogen monoxide carries an odd electron. Sulfur tetrafluoride holds ten.

Dr. Karmach

The octet is a pattern, not a law

Eight electrons fill an atom's s and p valence orbitals. Most main-group atoms reach that count. Three families do not, each for its own reason.

BF₃: six around B  ·  NO: 11 electrons, one unpaired  ·  SF₄: ten around S
incomplete octet · odd-electron molecule · expanded octet
period 3 or lower can expand · C, N, O, F stop at eight
a period-2 atom has four valence orbitals: room for eight, never more
Dr. Karmach

Incomplete octets: beryllium and boron

Boron and beryllium routinely stop short of eight. In BF₃, boron holds three bonds and six electrons, and the structure is stable as drawn.

BF₃: 3 + 3(7) = 24  ·  B: 3 bonds = 6 electrons
every F keeps its octet · boron does not reach eight
Dr. Karmach

Odd-electron molecules

An odd valence total can never pair into full octets. NO holds 11 electrons; one stays unpaired on nitrogen. The structure shows it as a single dot.

NO: 5 + 6 = 11 valence electrons
10 pair up · 1 electron remains single · no octet for N
Dr. Karmach

Expanded octets: period 3 and below

A period-2 atom has four valence orbitals, one s and three p: eight electrons at most. Atoms from period 3 down are larger, with more orbitals, so more pairs fit.

PF₅: 10 around P  ·  SF₄: 10 around S  ·  ICl₄⁻: 12 around I
only period-3-or-lower centers expand · C, N, O, F stop at eight
Dr. Karmach

The method

  1. Count the valence electrons.
  2. Build the skeleton, then the outer octets.
  3. Leftovers go on the central atom, past eight when it sits in period 3 or lower.
  4. Never expand a second-period atom.
Dr. Karmach

Worked example 1: phosphorus pentafluoride

Step 1 · Count the valence electrons

PF₅: 5 + 5(7) = 40
1 P (group 15 → 5) · 5 F (group 17 → 7) · 40 to place

Five fluorines must bond to one phosphorus. Draw the Lewis structure.

Dr. Karmach

Worked example 1: solution

PF₅: 5 + 5(7) = 40 valence electrons · skeleton: five P–F single bonds

Step 2 · Build the skeleton, then the outer octets

5 bonds: 5 × 2 = 10  ·  5 F × 3 lone pairs: 5 × 6 = 30
10 + 30 = 40 · every electron placed · every F has its octet
Dr. Karmach

Worked example 1: solution

PF₅: 5 + 5(7) = 40 valence electrons · skeleton: five P–F single bonds

Step 2 · Build the skeleton, then the outer octets

5 bonds: 5 × 2 = 10  ·  5 F × 3 lone pairs: 5 × 6 = 30
10 + 30 = 40 · every electron placed · every F has its octet
Ten electrons sit in the five P–F bonds and thirty complete the fluorines. All 40 are placed.
Dr. Karmach

Worked example 1: the expanded octet

Step 3 · Leftovers go on the central atom

40 − 10 − 30 = 0 leftover  ·  P: 5 bonds = 10 electrons
phosphorus exceeds eight through its bonds alone · period 3 → allowed

Dr. Karmach

Worked example 1: the expanded octet

Step 3 · Leftovers go on the central atom

40 − 10 − 30 = 0 leftover  ·  P: 5 bonds = 10 electrons
phosphorus exceeds eight through its bonds alone · period 3 → allowed

Ten electrons around phosphorus: an expanded octet carried by the bonds alone.
Dr. Karmach

Where this goes wrong

Expanding a second-period atom. Ten electrons around carbon or nitrogen is never right. Expansion starts in period 3; C, N, O, and F stop at eight.
Pairing the unpairable. NO holds 11 valence electrons. No structure pairs them all; one electron stays single, and the drawing must show it.
Dr. Karmach

Practice 1: naming the exception

molecule
1 BCl₃
2 ClO₂
3 PCl₅

Name the octet exception each molecule shows, in order.

  1. expanded · odd-electron · expanded
  2. odd-electron · odd-electron · expanded
  3. incomplete · odd-electron · expanded
  4. incomplete · incomplete · expanded
Dr. Karmach

Practice 1 answer: C

BCl₃: 3 + 3(7) = 24, B at 6  ·  ClO₂: 7 + 2(6) = 19, odd  ·  PCl₅: 5 bonds, P at 10
incomplete · odd-electron · expanded → answer C

A read the period of the chlorines instead of the center. Boron is in period 2 and stops at six. B took boron's own count, 3, as the molecule's; the total, 24, is even. D called ClO₂ incomplete because one atom falls short of eight; an odd total, 19, puts it in the odd-electron family.

Boron center: incomplete. Odd total: odd-electron. Five bonds on period-3 phosphorus: expanded. ✓
Dr. Karmach

Practice 2: sulfur hexafluoride

SF₆: 6 + 6(7) = 48 valence electrons · six S–F single bonds
each F carries 3 lone pairs · nothing is left over

How many electrons surround the sulfur atom?

  1. 48
  2. 36
  3. 18
  4. 12
Dr. Karmach

Practice 2 answer: D

S: 6 bonds × 2 = 12 electrons → answer D
period-3 sulfur holds all six bonds · an expanded octet

C added sulfur's own six valence electrons on top of the twelve in its bonds: 12 + 6 = 18; those six are already inside the bonds. A counted the whole pool: 6 + 6(7) = 48. B counted the fluorine lone pairs: 6 × 6 = 36.

Six bonds alone put 12 electrons on sulfur. The 36 lone-pair electrons live on the fluorines, not on the center.
Dr. Karmach

Practice 3: an unpaired electron

Which species carries an unpaired electron?

  1. NO₂⁻
  2. NO₂
  3. N₂O₄
  4. BF₃
Dr. Karmach

Practice 3 answer: B

NO₂: 5 + 2(6) = 17, odd → one electron stays unpaired → answer B
NO₂⁻: 5 + 2(6) + 1 = 18 · N₂O₄: 2(5) + 4(6) = 34 · BF₃: 3 + 3(7) = 24 · all even

A dropped the 1− charge: 5 + 2(6) = 17 looks odd, but the added electron makes 18, and 18 pairs fully. C judged by nitrogen's own count, 5; two nitrogens give 2(5) + 4(6) = 34, even. D took boron's short octet for an unpaired electron; BF₃ holds 24 electrons, all in pairs.

Only an odd total leaves a single electron. Two NO₂ molecules pair their odd electrons to form N₂O₄. ✓
Dr. Karmach

Worked example 2: boron trifluoride

Step 1 · Count the valence electrons

BF₃: 3 + 3(7) = 24
1 B (group 13 → 3) · 3 F (group 17 → 7) · 24 to place

Three fluorines bond to one boron. Draw the Lewis structure and count the electrons around boron.

Dr. Karmach

Worked example 2: solution

BF₃: 3 + 3(7) = 24 valence electrons · skeleton: three B–F single bonds

Step 2 · Build the skeleton, then the outer octets

3 bonds: 3 × 2 = 6  ·  3 F × 3 lone pairs: 3 × 6 = 18
6 + 18 = 24 · every electron placed · every F has its octet
Dr. Karmach

Worked example 2: solution

BF₃: 3 + 3(7) = 24 valence electrons · skeleton: three B–F single bonds
Step 2 · Build the skeleton, then the outer octets
3 bonds: 3 × 2 = 6  ·  3 F × 3 lone pairs: 3 × 6 = 18
6 + 18 = 24 · every electron placed · every F has its octet
Step 3 · Leftovers go on the central atom
24 − 6 − 18 = 0 leftover  ·  B: 3 bonds = 6 electrons
nothing is left for boron · B stops at six
Dr. Karmach

Worked example 2: solution

BF₃: 3 + 3(7) = 24 valence electrons · skeleton: three B–F single bonds
Step 2 · Build the skeleton, then the outer octets
3 bonds: 3 × 2 = 6  ·  3 F × 3 lone pairs: 3 × 6 = 18
6 + 18 = 24 · every electron placed · every F has its octet
Step 3 · Leftovers go on the central atom
24 − 6 − 18 = 0 leftover  ·  B: 3 bonds = 6 electrons
nothing is left for boron · B stops at six
All 24 electrons are placed, every fluorine is full, and boron holds six: an incomplete octet.
Dr. Karmach

Worked example 2: leave boron at six

Structure 1: B at 6  ·  Structure 2: B at 8 through one B=F double bond
both place all 24 · every F at 8 in both

The tempting fix Pull a fluorine lone pair into a B=F double bond (Structure 2). Reject it: boron, like beryllium, accepts fewer than eight.

Dr. Karmach

Worked example 2: leave boron at six

Structure 1: B at 6  ·  Structure 2: B at 8 through one B=F double bond
both place all 24 · every F at 8 in both

The tempting fix Pull a fluorine lone pair into a B=F double bond (Structure 2). Reject it: boron, like beryllium, accepts fewer than eight.

Structure 1 is BF₃: three single bonds, every F at eight, B at six. ✓
Dr. Karmach

Take-home: boron and beryllium stop short

If nothing is left and the center is boron or beryllium, stop at fewer than eight. Never pull an outer lone pair into a double bond just to complete its octet.

BF₃: 24 electrons, all paired  ·  every F at 8  ·  B at 6
incomplete octet: the center falls short, the total is even · never force a B or Be octet
Dr. Karmach

Your turn: borane, BH₃

BH₃: 3 + 3(1) = 6 valence electrons
skeleton: three B–H single bonds · each H is full with one bond, 2 electrons

Fill the blanks: electrons in the 3 B–H bonds · leftover for boron · electrons around B

Dr. Karmach

Your turn: borane, BH₃

BH₃: 3 + 3(1) = 6 valence electrons
skeleton: three B–H single bonds · each H is full with one bond, 2 electrons
3 × 2 = 6  ·  6 − 6 = 0 leftover  ·  B: 3 bonds = 6 electrons
incomplete octet on boron · nothing is left, and boron accepts six: the same call as BF₃

Dr. Karmach

Practice 4: beryllium chloride

BeCl₂: 2 + 2(7) = 16 valence electrons · both structures place all 16

Which structure is best, and how many electrons surround beryllium in it?

  1. Structure 1, 4 electrons
  2. Structure 2, 8 electrons
  3. Structure 1, 8 electrons
  4. Structure 2, 4 electrons
Dr. Karmach

Practice 4 answer: A

structure 1: Be has two single bonds: 2 + 2 = 4 electrons → answer A
each Cl keeps three lone pairs and one bond: 8 ✓ · Be, like B, accepts fewer than eight
Dr. Karmach

Practice 4 answer: A

structure 1: Be has two single bonds: 2 + 2 = 4 electrons → answer A
each Cl keeps three lone pairs and one bond: 8 ✓ · Be, like B, accepts fewer than eight
B forced the octet: pulling a Cl lone pair into each bond gives Be 4 + 4 = 8, the same move BF₃ rejected. C picked the right structure but assumed eight: two single bonds hold only 2 + 2 = 4. D counted each double bond as one pair: two double bonds put 4 + 4 = 8 around Be.
Beryllium, like boron, accepts fewer than eight. Cl–Be–Cl with single bonds: four electrons around Be. ✓
Dr. Karmach

Practice 5: fewer than eight

Which molecule keeps fewer than eight electrons on its central atom in its best Lewis structure?

  1. COCl₂
  2. NF₃
  3. SbCl₅
  4. BBr₃
Dr. Karmach

Practice 5 answer: D

BBr₃: 3 + 3(7) = 24 · 3 bonds (6) + 9 Br lone pairs (18) = 24 · 0 left
B: 3 bonds = 6 electrons · boron accepts fewer than eight → answer D
COCl₂: 4 + 6 + 2(7) = 24 · NF₃: 5 + 3(7) = 26 · SbCl₅: 5 + 5(7) = 40
C: one C=O + two C–Cl = 4 + 2 + 2 = 8 · N: 3 bonds + 1 lone pair = 8 · Sb: 5 bonds = 10

A stopped at single bonds, which leave carbon at six. Carbon is not boron: an O lone pair forms C=O and completes the octet. B skipped the leftovers: 26 − 24 = 2 go on nitrogen, 6 + 2 = 8. C mixed up the families: antimony holds 10, an expanded octet.

A center short of eight gets a multiple bond, unless it is boron or beryllium. Those two stop short. ✓
Dr. Karmach

Practice 6: the BF₄⁻ ion

BF₄⁻: boron bonded to four F
formed when BF₃ picks up a fluoride ion, F⁻

How many electrons surround boron in the Lewis structure of BF₄⁻?

  1. 6
  2. 8
  3. 4
  4. 3
Dr. Karmach

Practice 6 answer: B

BF₄⁻: 3 + 4(7) + 1 = 32 · 4 bonds (8) + 4 F × 3 lone pairs (24) = 32 · 0 left
B: 4 bonds = 8 electrons → answer B · the 1− charge supplies the 32nd electron

A kept boron at six, as in BF₃, with the fourth fluorine left as a separate F⁻. The ion bonds all four. C counted bonds, not electrons: 4 bonds hold 4 × 2 = 8. D took boron's own 3 valence electrons as its total; the bonds bring in fluorine's electrons too.

Boron stops at six only when nothing more bonds to it. A fourth fluoride gives it four bonds and a full octet. ✓
Dr. Karmach

Practice 7: three central atoms

I PCl₄⁺ · II SiF₆²⁻ · III BeH₂
central atoms: phosphorus · silicon · beryllium

Which central atoms hold a number of electrons other than eight?

  1. II only
  2. III only
  3. II and III
  4. I, II, and III
Dr. Karmach

Practice 7 answer: C

PCl₄⁺: 5 + 4(7) − 1 = 32 · SiF₆²⁻: 4 + 6(7) + 2 = 48 · BeH₂: 2 + 2(1) = 4
P: 4 bonds = 8 · Si: 6 bonds = 12, expanded · Be: 2 bonds = 4, incomplete → answer C

A missed the incomplete octet: two Be–H bonds give beryllium 2 + 2 = 4. B stopped silicon at eight as if it were carbon; period-3 silicon holds six bonds, 12 electrons. D added PCl₄⁺'s charge instead of subtracting it: 5 + 4(7) + 1 = 34 leaves 2 for phosphorus, 10 electrons.

Count each species with its charge, then read the center: eight, more than eight, or fewer. ✓
Dr. Karmach

Check yourself

  1. Which periods allow an expanded octet, and which four elements never expand?
  2. How many electrons surround boron in BF₃, and why is that structure left as an incomplete octet?

The count of bonds and lone pairs around a central atom, octet or expanded, is exactly what fixes a molecule's three-dimensional shape.

Dr. Karmach

4 · VSEPR & Molecular Shape

Predict a molecule's electron-pair geometry and its shape by counting the electron domains on the central atom and reading which corners lone pairs take.

Dr. Karmach

What sets a molecule's shape

Tie balloons at one knot and they push apart to the roomiest arrangement. Atoms bonded to a central atom spread out the very same way.

Dr. Karmach

Electron domains repel and spread apart

An electron domain is one group of electrons on the central atom: a bond or a lone pair. Like charges repel, so the domains spread as far apart as they can.

domains push to the farthest-apart arrangement
that arrangement, lone pairs included, sets the molecule's shape
Dr. Karmach

Counting the domains

Count the domains on the central atom: one for each bonded atom, plus one for each lone pair. A single, double, or triple bond counts as one domain, no matter how many pairs it holds.

CO₂: C bonded to 2 O by double bonds
2 bonded atoms + 0 lone pairs → 2 domains (each double bond counts once)
NH₃: N bonded to 3 H, plus 1 lone pair
3 bonded atoms + 1 lone pair → 4 domains
domains = X + E
X = atoms bonded to the central atom · E = lone pairs on the central atom
Dr. Karmach

From domain count to electron-pair geometry

The number of domains fixes how they arrange in space. Two domains sit at 180°, three at 120°, four at 109.5°. This spread is the electron-pair geometry.

Dr. Karmach

From geometry to molecular shape

Lone pairs take up domains but hold no atom. The molecular shape names only where the atoms sit. Four tetrahedral domains read as tetrahedral, trigonal pyramidal, or bent as lone pairs replace atoms.

Dr. Karmach

The common shapes side by side

memory hook: count the domains, then subtract the lone pairs from the name
2 → linear · 3 → trigonal planar, then bent · 4 → tetrahedral, then trigonal pyramidal, then bent
Dr. Karmach

The method

  1. Count the electron domains. One per bonded atom, one per lone pair; every bond counts once.
  2. Name the electron-pair geometry. 2 linear, 3 trigonal planar, 4 tetrahedral.
  3. Name the molecular shape. Keep atom positions; lone-pair corners stay empty.
Dr. Karmach

Guided example: oxygen difluoride

OF₂
only the formula · no bonds or lone pairs drawn yet

A formula does not show the lone pairs. Draw the Lewis structure first, then read X and E on oxygen.

Find the molecular shape of OF₂.

Dr. Karmach

Guided example: the Lewis structure

First · Draw the Lewis structure

OF₂: 6 + 2(7) = 20 valence electrons
F–O–F: 2 bonds use 4 · each F takes 6 more: 2 × 6 = 12 · 20 − 4 − 12 = 4 left on O

Oxygen is the central atom. The 4 leftover electrons stay on oxygen as two lone pairs.

Dr. Karmach

Guided example: the Lewis structure

First · Draw the Lewis structure

OF₂: 6 + 2(7) = 20 valence electrons
F–O–F: 2 bonds use 4 · each F takes 6 more: 2 × 6 = 12 · 20 − 4 − 12 = 4 left on O
Read X and E

Two fluorines bond to oxygen: X = 2. Two lone pairs sit on oxygen: E = 2.

Dr. Karmach

Guided example: the Lewis structure

First · Draw the Lewis structure

OF₂: 6 + 2(7) = 20 valence electrons
F–O–F: 2 bonds use 4 · each F takes 6 more: 2 × 6 = 12 · 20 − 4 − 12 = 4 left on O
Read X and E

Two fluorines bond to oxygen: X = 2. Two lone pairs sit on oxygen: E = 2.

Every atom has an octet, and 4 + 16 = 20 electrons are placed. ✓
Dr. Karmach

Guided example: the shape

OF₂: F–O–F with 2 lone pairs on O
from the Lewis structure: X = 2 bonded F · E = 2 lone pairs on O

Step 1 · Count the electron domains

X + E = 2 + 2 = 4 electron domains.

Dr. Karmach

Guided example: the shape

OF₂: F–O–F with 2 lone pairs on O
from the Lewis structure: X = 2 bonded F · E = 2 lone pairs on O
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry

Four domains spread to 109.5°. The electron-pair geometry is tetrahedral.

Dr. Karmach

Guided example: the shape

OF₂: F–O–F with 2 lone pairs on O
from the Lewis structure: X = 2 bonded F · E = 2 lone pairs on O
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry Step 3 · Name the molecular shape
OF₂ → bent
4 domains · tetrahedral geometry · 2 corners hold lone pairs
Dr. Karmach

Guided example: the shape

OF₂: F–O–F with 2 lone pairs on O
from the Lewis structure: X = 2 bonded F · E = 2 lone pairs on O
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry Step 3 · Name the molecular shape
OF₂ → bent
4 domains · tetrahedral geometry · 2 corners hold lone pairs
The formula alone hid the two lone pairs. The Lewis structure found them, and they bend the molecule.
Dr. Karmach

Worked example 1: methane

CH₄: C bonded to 4 H
central atom: carbon · 4 bonded H · 0 lone pairs on C

Methane's central carbon bonds to four hydrogens with no lone pairs left over. Give its electron-pair geometry and its molecular shape.

Dr. Karmach

Worked example 1: solution

CH₄: C bonded to 4 H
central atom: carbon · 4 bonded H · 0 lone pairs on C

Step 1 · Count the electron domains

Four bonded hydrogens and no lone pairs on carbon. Together that is 4 + 0 = 4 electron domains.

Dr. Karmach

Worked example 1: solution

CH₄: C bonded to 4 H
central atom: carbon · 4 bonded H · 0 lone pairs on C
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry

Four domains spread as far apart as possible, to 109.5°. The electron-pair geometry is tetrahedral.

Dr. Karmach

Worked example 1: solution

CH₄: C bonded to 4 H
central atom: carbon · 4 bonded H · 0 lone pairs on C
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry Step 3 · Name the molecular shape
CH₄ → tetrahedral
4 domains · 0 lone pairs · every corner holds an atom · 109.5°
Dr. Karmach

Worked example 1: solution

CH₄: C bonded to 4 H
central atom: carbon · 4 bonded H · 0 lone pairs on C
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry Step 3 · Name the molecular shape
CH₄ → tetrahedral
4 domains · 0 lone pairs · every corner holds an atom · 109.5°
No lone pairs, so every corner holds an atom and the shape matches the electron-pair geometry: tetrahedral.
Dr. Karmach

Worked example 1: the row in the table

CH₄: X = 4 bonded H · E = 0 lone pairs → AX₄
found: 4 domains · tetrahedral geometry · tetrahedral shape · 109.5°

Four atoms and no lone pairs: the AX₄ row. The geometry and the shape share one name. ✓
Dr. Karmach

Worked example 2: carbon dioxide

O=C=O: C bonded to 2 O by double bonds
central atom: carbon · 2 bonded O · 0 lone pairs on C

Carbon dioxide holds two carbon–oxygen double bonds. A common first attempt: two double bonds make four domains. Find the geometry and the shape.

Dr. Karmach

Worked example 2: solution

O=C=O: C bonded to 2 O by double bonds
central atom: carbon · 2 bonded O · 0 lone pairs on C

A common first attempt

2 double bonds = 4 domains?
counting each double bond as two: 2 × 2 = 4 ✗ · a bond is one domain however many pairs it holds

A double bond is one region of electrons, so it counts once. Two double bonds are two domains, not four.

Dr. Karmach

Worked example 2: solution

O=C=O: C bonded to 2 O by double bonds
central atom: carbon · 2 bonded O · 0 lone pairs on C
A common first attempt
2 double bonds = 4 domains?
counting each double bond as two: 2 × 2 = 4 ✗ · a bond is one domain however many pairs it holds
Step 1 · Count the electron domains

Two bonded oxygens and no lone pairs on carbon: 1 + 1 = 2 electron domains.

Dr. Karmach

Worked example 2: solution

O=C=O: C bonded to 2 O by double bonds
central atom: carbon · 2 bonded O · 0 lone pairs on C
A common first attempt
2 double bonds = 4 domains?
counting each double bond as two: 2 × 2 = 4 ✗ · a bond is one domain however many pairs it holds
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry

Two domains point straight apart, to 180°. The electron-pair geometry is linear.

Dr. Karmach

Worked example 2: solution

O=C=O: C bonded to 2 O by double bonds
central atom: carbon · 2 bonded O · 0 lone pairs on C
A common first attempt
2 double bonds = 4 domains?
counting each double bond as two: 2 × 2 = 4 ✗ · a bond is one domain however many pairs it holds
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry Step 3 · Name the molecular shape
CO₂ → linear
2 domains · 0 lone pairs · both corners hold an atom · 180°
Dr. Karmach

Worked example 2: solution

O=C=O: C bonded to 2 O by double bonds
central atom: carbon · 2 bonded O · 0 lone pairs on C
A common first attempt
2 double bonds = 4 domains?
counting each double bond as two: 2 × 2 = 4 ✗ · a bond is one domain however many pairs it holds
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry Step 3 · Name the molecular shape
CO₂ → linear
2 domains · 0 lone pairs · both corners hold an atom · 180°
Each double bond is one domain, so carbon has two. Two domains can only point 180° apart: a linear molecule.
Dr. Karmach

Worked example 2: the row in the table

CO₂: X = 2 bonded O · E = 0 lone pairs → AX₂
found: 2 domains · linear geometry · linear shape · 180°

Two atoms and no lone pairs: the AX₂ row. Each double bond counts once, so the row stays AX₂. ✓
Dr. Karmach

Take-home: a bond is one domain

O=C=O → 2 domains → linear (180°)
each double bond counts once: 1 + 1 = 2 ✓
counting each double bond twice → 4 domains → a tetrahedral guess
2 × 2 = 4 ✗ · the extra domains would bend a straight molecule

Bond order does not change the domain count. A single, double, or triple bond is one region of electrons, so it claims one domain.

Dr. Karmach

Your turn: ammonia

NH₃: N bonded to 3 H, with 1 lone pair on N
central atom: nitrogen · 3 bonded H · 1 lone pair
step count result
1 · domains 3 bonded + 1 lone pair domains
2 · electron-pair geometry from 4 domains
3 · molecular shape 3 atoms, 1 corner a lone pair

Fill the three results.

Dr. Karmach

Your turn: ammonia

NH₃: N bonded to 3 H, with 1 lone pair on N
central atom: nitrogen · 3 bonded H · 1 lone pair
step count result
1 · domains 3 bonded + 1 lone pair domains
2 · electron-pair geometry from 4 domains
3 · molecular shape 3 atoms, 1 corner a lone pair

Fill the three results.

NH₃ → trigonal pyramidal
3 + 1 = 4 domains · tetrahedral geometry · 1 corner empty · angle ≈ 107°
Dr. Karmach

Where this goes wrong

Reporting the electron-pair geometry as the shape. Water has four domains, a tetrahedral geometry. But two corners are lone pairs. The shape names only the atoms: bent, not tetrahedral.
Ignoring the lone pairs. Arrange only NH₃'s three bonded atoms and you get a flat trigonal planar. The lone pair takes a corner too, pressing the atoms into a trigonal pyramid.
Counting a double bond as two domains. SO₂ has two bonded oxygens plus one lone pair. Count the S=O double bond as two and you reach four domains. Each bond is one domain: 2 + 1 = 3 domains, a bent molecule.
Dr. Karmach

Practice 1

NF₃: N bonded to 3 F, with 1 lone pair on N
central atom: nitrogen · 3 bonded F · 1 lone pair

Nitrogen trifluoride has three bonded fluorines and one lone pair on nitrogen. What is its molecular shape?

  1. Trigonal pyramidal: three bonded atoms with the lone pair pressing them down
  2. Tetrahedral: the four electron domains arrange as a tetrahedron
  3. Trigonal planar: the three fluorines spread evenly around nitrogen
  4. Bent: the lone pair leaves only a bent arrangement
Dr. Karmach

Practice 1 answer: A

NF₃ → trigonal pyramidal → answer A
3 bonded F + 1 lone pair = 4 domains · tetrahedral geometry · 1 corner empty

B named the electron-pair geometry, not the shape: the lone pair takes a corner, so the atoms are not tetrahedral. C ignored the lone pair; three bonded atoms alone would be trigonal planar, but the fourth corner is filled. D miscounts: four domains, not three, so the base is a tetrahedron, not a triangle.

Four domains, one a lone pair: the three fluorines press down into a pyramid. Trigonal pyramidal.
Dr. Karmach

Practice 2

PCl₃
phosphorus trichloride, a starting material for weed killers

Which is the molecular shape of PCl₃?

  1. Tetrahedral: four electron domains around phosphorus
  2. Trigonal pyramidal: three chlorines and one lone pair on phosphorus
  3. Trigonal planar: three chlorines and no lone pair on phosphorus
  4. Bent: three domains, one of them a lone pair
Dr. Karmach

Practice 2 answer: B

PCl₃: 5 + 3(7) = 26 · 3 bonds use 3 × 2 = 6 · each Cl takes 6: 3 × 6 = 18 · 26 − 6 − 18 = 2 left → 1 lone pair on P
X = 3 · E = 1 · 3 + 1 = 4 domains · tetrahedral geometry · AX₃E, trigonal pyramidal → answer B

A named the electron-pair geometry; one corner holds the lone pair, not an atom. C stopped after the outer octets: 26 − 6 − 18 = 2 electrons remain, and they sit on phosphorus. D counted three domains with one a lone pair, which leaves room for only two chlorines. PCl₃ has three bonded Cl plus the lone pair: 3 + 1 = 4 domains.

The formula showed three chlorines. The Lewis structure showed the lone pair that makes the pyramid. ✓
Dr. Karmach

Worked example 3: sulfur dioxide

O=S–O: S bonded to 2 O, with 1 lone pair on S
central atom: sulfur · 2 bonded O · 1 lone pair · one bond is double

Sulfur dioxide has two bonded oxygens, one of them a double bond, and a lone pair on sulfur. Give its electron-pair geometry and its molecular shape.

Dr. Karmach

Worked example 3: solution

O=S–O: S bonded to 2 O, with 1 lone pair on S
central atom: sulfur · 2 bonded O · 1 lone pair · one bond is double

Step 1 · Count the electron domains

Two bonded oxygens count as two domains: the double bond counts once. Add the lone pair: 2 + 1 = 3 electron domains.

Dr. Karmach

Worked example 3: solution

O=S–O: S bonded to 2 O, with 1 lone pair on S
central atom: sulfur · 2 bonded O · 1 lone pair · one bond is double
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry

Three domains spread to 120°. The electron-pair geometry is trigonal planar.

Dr. Karmach

Worked example 3: solution

O=S–O: S bonded to 2 O, with 1 lone pair on S
central atom: sulfur · 2 bonded O · 1 lone pair · one bond is double
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry Step 3 · Name the molecular shape
SO₂ → bent
3 domains · trigonal planar geometry · 1 corner a lone pair · angle just under 120°
Dr. Karmach

Worked example 3: solution

O=S–O: S bonded to 2 O, with 1 lone pair on S
central atom: sulfur · 2 bonded O · 1 lone pair · one bond is double
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry Step 3 · Name the molecular shape
SO₂ → bent
3 domains · trigonal planar geometry · 1 corner a lone pair · angle just under 120°
Three domains, one a lone pair, leave two oxygens in a bent line. The lone pair squeezes the angle a little below 120°.
Dr. Karmach

Worked example 3: the row in the table

SO₂: X = 2 bonded O · E = 1 lone pair → AX₂E
found: 3 domains · trigonal planar geometry · bent shape · just under 120°

Two atoms and one lone pair: the AX₂E row, inside the trigonal planar group. ✓
Dr. Karmach

Summary: domains, geometry, shape

Count the bonded atoms (X) and lone pairs (E), then read the row across.

Dr. Karmach

Worked example 4: water

H–O–H: O bonded to 2 H, with 2 lone pairs on O
central atom: oxygen · 2 bonded H · 2 lone pairs on O

Water's oxygen bonds to two hydrogens and keeps two lone pairs. Count the domains, then read its row for the electron-pair geometry, the shape, and the angle.

Dr. Karmach

Worked example 4: solution

H–O–H: O bonded to 2 H, with 2 lone pairs on O
central atom: oxygen · 2 bonded H · 2 lone pairs on O

Step 1 · Count the electron domains

Two bonded hydrogens and two lone pairs on oxygen: 2 + 2 = 4 electron domains.

Dr. Karmach

Worked example 4: solution

H–O–H: O bonded to 2 H, with 2 lone pairs on O
central atom: oxygen · 2 bonded H · 2 lone pairs on O
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry

Four domains land on the AX₂E₂ row. The electron-pair geometry is tetrahedral.

Dr. Karmach

Worked example 4: solution

H–O–H: O bonded to 2 H, with 2 lone pairs on O
central atom: oxygen · 2 bonded H · 2 lone pairs on O
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry Step 3 · Name the molecular shape
H₂O → AX₂E₂ → bent
4 domains · tetrahedral geometry · 2 corners hold lone pairs · angle ≈ 104.5°
Dr. Karmach

Worked example 4: solution

H–O–H: O bonded to 2 H, with 2 lone pairs on O
central atom: oxygen · 2 bonded H · 2 lone pairs on O
Step 1 · Count the electron domains Step 2 · Name the electron-pair geometry Step 3 · Name the molecular shape
H₂O → AX₂E₂ → bent
4 domains · tetrahedral geometry · 2 corners hold lone pairs · angle ≈ 104.5°
Two of the four corners hold lone pairs. The two hydrogens are left in a bent line, near 104.5°.
Dr. Karmach

Worked example 4: the row in the table

H₂O: X = 2 bonded H · E = 2 lone pairs → AX₂E₂
found: 4 domains · tetrahedral geometry · bent shape · about 104.5°

Two atoms and two lone pairs: the AX₂E₂ row. Same shape name as SO₂, a different row and a smaller angle. ✓
Dr. Karmach

Practice 3

NO₂⁻
the nitrite ion, used to cure bacon and ham

What are the shape and the bond angle of the nitrite ion?

  1. Tetrahedral, 109.5°
  2. Trigonal planar, 120°
  3. Bent, <109.5°
  4. Bent, <120°
  5. Linear, 180°
Dr. Karmach

Practice 3 answer: D

NO₂⁻: 5 + 2(6) + 1 = 18 · 2 bonds use 4 · each O takes 6: 2 × 6 = 12 · 18 − 4 − 12 = 2 left → 1 lone pair on N
N has only 4 + 2 = 6 → one O shares a pair: O=N–O⁻, 2 resonance forms · X = 2 · E = 1 either way · 3 domains · AX₂E, bent, just under 120° → answer D

B named the electron-pair geometry; the lone pair takes a corner, so the atoms are bent. C counted the N=O double bond as two domains: 2 + 1 + 1 = 4, a tetrahedral base. A made the same count and then named that geometry. E subtracted the charge: 5 + 2(6) − 1 = 16 leaves 16 − 4 − 12 = 0 for N, so O=N=O would be linear.

The 1− charge adds the electron that finishes nitrogen's lone pair. The N=O double bond still counts once. ✓
Dr. Karmach

Practice 4

ClO₃⁻: Cl bonded to 3 O
a student draws three Cl–O bonds, no lone pair on Cl, and names the shape trigonal planar

The chlorate ion, ClO₃⁻, is found in match heads. Evaluate the work.

  1. Correct: three bonded atoms and no lone pair give trigonal planar, 120°
  2. Wrong: chlorine keeps one lone pair, so four domains make the shape tetrahedral
  3. Wrong: chlorine keeps one lone pair, so four domains make the shape trigonal pyramidal
  4. Wrong: chlorine keeps one lone pair, so four domains make the shape bent
Dr. Karmach

Practice 4 answer: C

ClO₃⁻: 7 + 3(6) + 1 = 26 · 3 bonds use 6 · each O takes 6: 3 × 6 = 18 · 26 − 6 − 18 = 2 left → 1 lone pair on Cl
Cl: 6 + 2 = 8 ✓ · X = 3 · E = 1 · 3 + 1 = 4 domains · tetrahedral geometry · AX₃E, trigonal pyramidal, just under 109.5° → answer C

A dropped the leftover pair: the charge's electron makes 26, and 2 of them stay on chlorine. B named the electron-pair geometry; one corner holds the lone pair, not an atom. D took the water row: bent needs two lone pairs and two atoms, and ClO₃⁻ has three bonded O and one lone pair.

Same row as NH₃ and PCl₃: three atoms, one lone pair. Count the charge before reading the shape. ✓
Dr. Karmach

Extra practice 1

BI₃
boron triiodide, used to cleave ethers in organic synthesis

By VSEPR, how many degrees separate two B–I bonds in BI₃?

  1. 109.5
  2. 90
  3. 120
  4. 107
Dr. Karmach

Extra practice 1 answer: C

BI₃: 3 + 3(7) = 24 · 3 bonds use 3 × 2 = 6 · each I takes 6: 3 × 6 = 18 · 24 − 6 − 18 = 0 left on B
B holds 6 electrons, an incomplete octet · X = 3 · E = 0 · 3 + 0 = 3 domains · trigonal planar, 120° → answer C

D forced boron's octet with a lone pair. No electrons remain for one, so the 3 + 1 = 4 domains of a 107° pyramid never form. A added the same lone pair and took the tetrahedral angle, 109.5°. B read the angle off the flat drawing; three domains spread to 120°, not 90°.

Boron stops at six electrons, as in BF₃. Three domains and no lone pair keep the molecule flat at 120°. ✓
Dr. Karmach

Extra practice 2

ClO₂⁺
the chloryl ion

For the chloryl ion, name the electron-pair geometry, then the molecular shape.

  1. Linear, then linear
  2. Tetrahedral, then bent
  3. Trigonal planar, then trigonal planar
  4. Tetrahedral, then trigonal pyramidal
  5. Trigonal planar, then bent
Dr. Karmach

Extra practice 2 answer: E

ClO₂⁺: 7 + 2(6) − 1 = 18 · 2 bonds use 4 · each O takes 6: 2 × 6 = 12 · 18 − 4 − 12 = 2 left → 1 lone pair on Cl
Cl has only 4 + 2 = 6 → one O shares a pair: O=Cl–O, Cl at 2 + 4 + 2 = 8 · X = 2 · E = 1 · 2 + 1 = 3 domains · AX₂E: trigonal planar, then bent → answer E

B added the charge: 7 + 2(6) + 1 = 20 leaves 20 − 4 − 12 = 4, two lone pairs and the 2 + 2 = 4 domains of chlorite, ClO₂⁻; a 1+ ion has one electron fewer. A dropped the leftover pair: 2 of the 18 electrons stay on chlorine as a third domain. C named the electron-pair geometry twice; the lone pair takes a corner, so the atoms are bent. D counted the Cl=O double bond as two domains: 2 + 1 + 1 = 4, then read a pyramid.

One electron fewer than chlorite removes one of chlorine's two lone pairs. Three domains, one of them a lone pair: bent. ✓
Dr. Karmach

Extra practice 3

NH₃: trigonal pyramidal
3 bonded H + 1 lone pair on N · 4 domains

Which species has the same molecular shape as ammonia?

  1. NO₃⁻
  2. SO₃
  3. NH₄⁺
  4. H₃O⁺
Dr. Karmach

Extra practice 3 answer: D

H₃O⁺: 6 + 3(1) − 1 = 8 · 3 bonds use 6 · 8 − 6 = 2 left → 1 lone pair on O
X = 3 · E = 1 · 3 + 1 = 4 domains · AX₃E, trigonal pyramidal: the same counts as NH₃ → answer D

A gave nitrogen a lone pair, as in NH₃. NO₃⁻ has 5 + 3(6) + 1 = 24 electrons, and 24 − 6 − 18 = 0 left; N at 6 → one O shares a pair, N=O: 3 domains, trigonal planar. B counted the S=O double bond twice: 3 + 1 = 4 domains around three atoms. SO₃ has 6 + 3(6) = 24, none left on S; S at 6 → one O shares a pair, S=O: 3 + 0 = 3 domains, trigonal planar. C matched the elements, not the counts. NH₄⁺ has 5 + 4(1) − 1 = 8 electrons, all in four N–H bonds: tetrahedral.

The same shape needs the same X and E, not the same central atom. H₃O⁺ and NH₃ are both AX₃E. ✓
Dr. Karmach

Check yourself

  1. Draw the Lewis structure of PH₃. Count X and E on phosphorus, then name the electron-pair geometry and the shape.
  2. Why do CO₂ and SO₂ have different shapes? Draw both Lewis structures and name each one's AXE row.

Shape sets polarity. Two equal bond dipoles cancel when they point exactly opposite, as in linear CO₂. A bent or pyramidal shape leaves them pointing partly the same way, so the molecule is polar. Combining these bond dipoles with the molecular shape shows whether the whole molecule is polar.

Dr. Karmach

5 · Molecular Polarity

Decide whether a whole molecule is polar by combining its bond dipoles with its shape: symmetric shapes with identical outer atoms cancel the dipoles to nonpolar, while lopsided shapes or a central lone pair leave a net dipole.

Dr. Karmach

Why the plate stays cool

A microwave heats the soup, not the dry plate under it. Water molecules are lopsided, so the oven's field keeps twisting them. That twisting is the heat.

Dr. Karmach

The shape decides, not the bonds

Each polar bond carries a dipole toward its more electronegative atom. The molecule is polar only when these dipoles do not cancel. The shape decides whether they cancel.

CO₂: polar bonds, the dipoles cancel
nonpolar molecule
H₂O: polar bonds, the dipoles add
polar molecule
Dr. Karmach

Every polar bond is an arrow

Draw each polar bond as a dipole arrow. It points to the more electronegative atom, the end that pulls the shared electrons closer. A bigger electronegativity difference means a stronger pull.

Dr. Karmach

When arrows cancel, and when they add

Identical arrows arranged evenly around the center cancel, and the molecule is nonpolar. A lopsided shape, or a central lone pair, leaves a net arrow, and the molecule is polar.

Dr. Karmach

When a molecule is nonpolar

A molecule with a lone pair on its central atom is polar. Otherwise it is nonpolar when every bond is nonpolar, or when its polar bonds cancel (identical outer atoms).

Dr. Karmach

The method

  1. Recall the shape from VSEPR.
  2. Draw the bond dipoles: one arrow per bond, toward the more electronegative atom.
  3. Add the arrows. Identical arrows in a symmetric shape cancel; a leftover arrow means polar.
Dr. Karmach

Worked example 1: carbon dioxide

CO₂: O=C=O
two C=O bonds · wanted: polar or nonpolar?

Carbon dioxide has two polar C=O bonds.

A common first answer: polar bonds, so the molecule is polar. Test it against the shape.

Dr. Karmach

Worked example 1: solution

CO₂: O=C=O
two C=O bonds · wanted: polar or nonpolar?

Step 1 · Recall the shape

Carbon has two bonding groups and no lone pairs. VSEPR gives a linear molecule: the two oxygens sit 180° apart.

Dr. Karmach

Worked example 1: solution

CO₂: O=C=O
two C=O bonds · wanted: polar or nonpolar?
Step 1 · Recall the shape Step 2 · Draw the bond dipoles
ΔEN(C=O): 3.44 − 2.55 = 0.89 · each bond polar, arrow toward O

Both arrows point outward, away from carbon, toward the oxygens.

Dr. Karmach

Worked example 1: solution

CO₂: O=C=O
two C=O bonds · wanted: polar or nonpolar?
Step 1 · Recall the shape Step 2 · Draw the bond dipoles
ΔEN(C=O): 3.44 − 2.55 = 0.89 · each bond polar, arrow toward O
Step 3 · Add the arrows
0.89 toward one O − 0.89 toward the other O = 0 net

The two arrows pull in exactly opposite directions and cancel. No net arrow. Nonpolar.

Dr. Karmach

Worked example 1: solution

CO₂: O=C=O
two C=O bonds · wanted: polar or nonpolar?
Step 1 · Recall the shape Step 2 · Draw the bond dipoles
ΔEN(C=O): 3.44 − 2.55 = 0.89 · each bond polar, arrow toward O
Step 3 · Add the arrows
0.89 toward one O − 0.89 toward the other O = 0 net
The C=O bonds are polar, yet CO₂ is nonpolar. Its linear shape aims the two equal arrows in opposite directions.
Dr. Karmach

Worked example 1: the route on the flowchart

CO₂: O=C=O, linear
no lone pair on C · C=O polar (0.89) · two identical O atoms · found: nonpolar

No lone pair on carbon, polar bonds, identical outer atoms: the two arrows cancel.
Dr. Karmach

Take-home: polar bonds do not make a polar molecule

CO₂: two polar C=O bonds, linear
symmetric: the two arrows cancel → nonpolar
H₂O: two polar O–H bonds, bent
lopsided: the two arrows add → polar

Both molecules have polar bonds. The linear shape cancels them; the bent shape does not. Polar bonds alone are not enough. The shape decides.

Dr. Karmach

Worked example 2: water

H₂O: two O–H bonds
two lone pairs on oxygen · wanted: polar or nonpolar?

Water has two polar O–H bonds and two lone pairs on its oxygen.

Apply the three steps.

Dr. Karmach

Worked example 2: solution

H₂O: two O–H bonds
two lone pairs on oxygen · wanted: polar or nonpolar?

Step 1 · Recall the shape

Oxygen has two bonding groups and two lone pairs. VSEPR gives a bent molecule; the two O–H bonds meet at about 104.5°.

Dr. Karmach

Worked example 2: solution

H₂O: two O–H bonds
two lone pairs on oxygen · wanted: polar or nonpolar?
Step 1 · Recall the shape Step 2 · Draw the bond dipoles
ΔEN(O–H): 3.44 − 2.20 = 1.24 · each bond polar, arrow toward O

Both arrows point from the hydrogens up toward the oxygen.

Dr. Karmach

Worked example 2: solution

H₂O: two O–H bonds
two lone pairs on oxygen · wanted: polar or nonpolar?
Step 1 · Recall the shape Step 2 · Draw the bond dipoles
ΔEN(O–H): 3.44 − 2.20 = 1.24 · each bond polar, arrow toward O
Step 3 · Add the arrows
arrow toward O + arrow toward O → one net arrow through O

The two arrows point the same way, so they reinforce instead of cancel. A net arrow runs through the oxygen. Polar.

Dr. Karmach

Worked example 2: solution

H₂O: two O–H bonds
two lone pairs on oxygen · wanted: polar or nonpolar?
Step 1 · Recall the shape Step 2 · Draw the bond dipoles
ΔEN(O–H): 3.44 − 2.20 = 1.24 · each bond polar, arrow toward O
Step 3 · Add the arrows
arrow toward O + arrow toward O → one net arrow through O
Both molecules have polar bonds, opposite results. Water's bent shape lets the two arrows add, and the lone pairs keep it from ever being symmetric.
Dr. Karmach

Worked example 2: the route on the flowchart

H₂O: bent, two lone pairs on O
two lone pairs on O · O–H polar (1.24) · found: polar

The first question settles it: lone pairs on the central oxygen leave the molecule lopsided. ✓
Dr. Karmach

Your turn: ammonia

NH₃: three N–H bonds, one lone pair on nitrogen
ΔEN(N–H) = 3.04 − 2.20 = 0.84 → each bond polar
shape: · three arrows toward N · they → NH₃ is

Recall the shape, draw the three arrows, then decide whether they cancel.

Dr. Karmach

Your turn: ammonia

NH₃: three N–H bonds, one lone pair on nitrogen
ΔEN(N–H) = 3.04 − 2.20 = 0.84 → each bond polar
shape: · three arrows toward N · they → NH₃ is

Recall the shape, draw the three arrows, then decide whether they cancel.

shape: trigonal pyramidal · three arrows toward N, tilted to one side · they do not cancel → NH₃ is polar

The lone pair pushes the three N–H bonds to one side, so their arrows cannot balance. A net arrow points through the nitrogen.

Dr. Karmach

Where this goes wrong

Polar bonds, so a polar molecule. CO₂ has two polar C=O bonds, and the leap to "so CO₂ is polar" skips the shape. Linear and symmetric, its two arrows cancel: nonpolar. The bonds do not decide; the shape does.
Calling a symmetric shape lopsided. SO₃ is trigonal planar with three identical S=O bonds and no lone pair on sulfur. Claiming the arrows "add up" ignores that three equal arrows 120° apart cancel exactly. Identical outer atoms in an even arrangement balance.
Nonpolar for the wrong reason. CCl₄ is nonpolar, but not because its bonds are nonpolar. Each C–Cl bond is polar. The molecule is nonpolar because the tetrahedral shape cancels the four arrows.
Missing the lone pair. Treating NH₃ as a flat, even molecule calls it nonpolar. The lone pair on nitrogen tilts the three N–H arrows to one side, and they no longer cancel: polar.
Dr. Karmach

Practice 1

BCl₃: three B–Cl bonds, trigonal planar, no lone pair on boron
ΔEN(B–Cl) = 3.16 − 2.04 = 1.12 → each bond polar

Boron trichloride has three identical polar bonds in a flat triangle. Polar or nonpolar, and why?

  1. Polar: the trigonal planar shape places the three arrows asymmetrically, so they add up
  2. Polar: it contains polar B–Cl bonds, so the whole molecule must be polar
  3. Nonpolar: the B–Cl bonds are polar, but the trigonal planar shape is symmetric, so the three arrows cancel
  4. Nonpolar: none of its B–Cl bonds are polar in the first place
Dr. Karmach

Practice 1 answer: C

BCl₃ → nonpolar → answer C
three polar B–Cl arrows, 120° apart, cancel → no net arrow
trigonal planar, symmetric · three arrows toward Cl, 120° apart → cancel: nonpolar

B took polar bonds as proof of a polar molecule and skipped the shape: the symmetric triangle cancels the three equal arrows. A called the symmetric shape lopsided, but three identical arrows 120° apart balance exactly. D denied the bonds are polar. ΔEN(B–Cl) = 3.16 − 2.04 = 1.12, so each bond is polar, and the molecule is nonpolar because of the shape, not because the bonds are nonpolar.

Three equal arrows spread evenly around the boron sum to zero. Symmetric polar bonds → nonpolar. ✓
Dr. Karmach

Practice 2: carbon disulfide

CS₂: carbon disulfide
electronegativity: C = 2.55 · S = 2.58 · wanted: polar or nonpolar, and why

Is carbon disulfide polar or nonpolar?

  1. Nonpolar: C and S pull almost equally, and the linear shape would cancel any dipoles
  2. Polar: S out-pulls C, so each bond is polar and so is the molecule
  3. Polar: a lone pair on carbon bends the molecule
  4. Polar: the lone pairs on the sulfur atoms bend the molecule
Dr. Karmach

Practice 2 answer: A

CS₂: S=C=S · 4 + 2(6) = 16 valence e⁻
two C=S bonds use 8 · four lone pairs on the S atoms use 8 · none left on C · linear
ΔEN(C=S): 2.58 − 2.55 = 0.03 · under 0.4: nonpolar bonds → nonpolar → answer A

B skipped the difference: 0.03 is far under 0.4, and even polar bonds would cancel in a straight line. C gave carbon a lone pair; its four valence electrons all go into the two double bonds. D bent the molecule with the outer atoms' lone pairs; only lone pairs on the central atom set the shape.

Nonpolar twice over: the bonds are nonpolar, and the linear shape is symmetric. ✓
Dr. Karmach

Practice 3: hydrogen sulfide

H₂S: hydrogen sulfide
electronegativity: H = 2.20 · S = 2.58 · wanted: polar or nonpolar, and why

Is hydrogen sulfide polar or nonpolar?

  1. Nonpolar: the molecule is linear, so the two S–H arrows cancel
  2. Nonpolar: ΔEN(S–H) is under 0.4, so the bonds are nonpolar
  3. Nonpolar: sulfur's two lone pairs sit on opposite sides and balance each other
  4. Polar: two lone pairs on sulfur make the molecule bent and lopsided
Dr. Karmach

Practice 3 answer: D

H₂S: 2(1) + 6 = 8 valence e⁻
two S–H bonds use 4 · 8 − 4 = 4 left = 2 lone pairs on S · 4 domains · bent
lone pair on the central S? yes → polar → answer D

A missed the two lone pairs and drew H₂S straight, like CS₂. B skipped the first question: 2.58 − 2.20 = 0.38 is under 0.4, but a central lone pair makes the molecule polar anyway. C read the flat drawing as the shape; four domains spread in three dimensions, and both lone pairs sit on one side of sulfur.

Two outer atoms in CS₂ and H₂S, opposite answers: the lone pairs on sulfur make the difference. ✓
Dr. Karmach

Worked example 3: two tetrahedral molecules

CCl₄ and CHCl₃: both tetrahedral, carbon at the center
four C–Cl bonds · CHCl₃ swaps one Cl for H · wanted: each polar or nonpolar?

Two molecules with the same tetrahedral shape. CCl₄ has four C–Cl bonds; CHCl₃ replaces one chlorine with a hydrogen.

Judge each: polar or nonpolar?

Dr. Karmach

Worked example 3: shape and dipoles

CCl₄ and CHCl₃: both tetrahedral, carbon at the center
wanted: each molecule polar or nonpolar?

Step 1 · Recall the shape

Both are tetrahedral: four bonding groups on carbon, no lone pairs, the outer atoms 109.5° apart.

Dr. Karmach

Worked example 3: shape and dipoles

CCl₄ and CHCl₃: both tetrahedral, carbon at the center
wanted: each molecule polar or nonpolar?
Step 1 · Recall the shape Step 2 · Draw the bond dipoles
ΔEN(C–Cl): 3.16 − 2.55 = 0.61 · ΔEN(C–H): 2.55 − 2.20 = 0.35 · C–Cl polar · C–H under 0.4, nearly nonpolar

Each C–Cl arrow points toward its chlorine; the weaker C–H arrow points toward carbon.

Dr. Karmach

Worked example 3: shape and dipoles

CCl₄ and CHCl₃: both tetrahedral, carbon at the center
wanted: each molecule polar or nonpolar?
Step 1 · Recall the shape Step 2 · Draw the bond dipoles
ΔEN(C–Cl): 3.16 − 2.55 = 0.61 · ΔEN(C–H): 2.55 − 2.20 = 0.35 · C–Cl polar · C–H under 0.4, nearly nonpolar
The C–Cl bonds are polar. Whether the molecule is polar now depends only on how the four arrows are arranged.
Dr. Karmach

Worked example 3: adding the arrows

same tetrahedral shape, one outer atom swapped
CCl₄ → nonpolar · CHCl₃ → polar

Step 3 · Add the arrows

CCl₄'s four identical arrows cancel; swapping one chlorine for hydrogen leaves the three chlorine arrows unbalanced, so a net arrow remains: polar. ✓
Dr. Karmach

Worked example 3: the route on the flowchart

CCl₄ and CHCl₃: tetrahedral, no lone pair on C
no lone pair on C · C–Cl polar (0.61) · CCl₄: four identical Cl → nonpolar · CHCl₃: H and Cl mixed → polar

Same shape, same first two answers. The outer atoms alone split the two molecules.
Dr. Karmach

Practice 4: dichloromethane

CH₂Cl₂: dichloromethane
electronegativity: H = 2.20 · C = 2.55 · Cl = 3.16 · wanted: polar or nonpolar, and why

Is dichloromethane polar or nonpolar?

  1. Nonpolar: it is tetrahedral with no lone pair on carbon, so the arrows cancel
  2. Nonpolar: the two C–Cl arrows point opposite ways, as drawn on paper, and cancel
  3. Polar: the outer atoms are not identical, so the arrows do not cancel
  4. Polar: its bonds are polar, and polar bonds always make a polar molecule
Dr. Karmach

Practice 4 answer: C

CH₂Cl₂: tetrahedral, no lone pair on C
outer atoms: 2 H and 2 Cl, not identical · ΔEN(C–Cl) = 0.61 · ΔEN(C–H) = 0.35
two strong C–Cl arrows + two weak C–H → unbalanced: polar → answer C

A stopped at the lone-pair question; a tetrahedral shape cancels only when all four outer atoms are identical, as in CCl₄. B trusted the flat drawing; in three dimensions the two C–Cl bonds sit 109.5° apart, never opposite, so their arrows add. D used a rule CCl₄ breaks: four polar bonds, nonpolar molecule.

Swap outer atoms on a symmetric shape and the balance breaks: polar. ✓
Dr. Karmach

Practice 5

SiF₄ · PCl₃ · OCS · CF₄
wanted: every nonpolar molecule in the set

Which of these molecules are nonpolar?

  1. SiF₄, OCS and CF₄
  2. SiF₄ and CF₄
  3. SiF₄, PCl₃ and CF₄
  4. None of them: every one contains polar bonds
Dr. Karmach

Practice 5 answer: B

nonpolar: SiF₄ and CF₄ → answer B
SiF₄, CF₄ tetrahedral, four identical arrows cancel · PCl₃ trigonal pyramidal, lone pair → polar · OCS linear, O and S pull unequally → polar

A read OCS as symmetric like CO₂; linear cancels only when both outer atoms are identical, and C=O out-pulls C=S. C missed the lone pair on phosphorus and treated PCl₃ as a flat triangle; three bonds plus one lone pair make it pyramidal and polar. D took polar bonds as proof of a polar molecule; SiF₄ and CF₄ have polar bonds and cancel by shape.

Nonpolar needs both: a symmetric shape and identical outer atoms. ✓
Dr. Karmach

Practice 6

CH₄ · NF₃ · SO₂ · CH₃Br
wanted: the one nonpolar molecule

Which one of these molecules is nonpolar?

  1. CH₄
  2. NF₃
  3. SO₂
  4. CH₃Br
Dr. Karmach

Practice 6 answer: A

CH₄ → nonpolar → answer A
NF₃: lone pair on N, pyramidal · SO₂: lone pair on S, bent · CH₃Br: one Br among three H
CH₄: tetrahedral, no lone pair on C · four identical C–H arrows → cancel: nonpolar → answer A

B stopped at three identical fluorines; identical outer atoms cancel only around a symmetric center, and the lone pair on nitrogen pushes all three N–F arrows to one side. C drew SO₂ straight like CO₂; the lone pair on sulfur bends it, and the two sulfur–oxygen arrows add. D stopped at the tetrahedral shape; one Br among three H leaves the C–Br arrow with no equal partner.

CH₄ and CH₃Br share the tetrahedral shape; only CH₄ keeps four identical outer atoms. ✓
Dr. Karmach

Practice 7

CH₂O: formaldehyde, C is the central atom
electronegativity: H = 2.20 · C = 2.55 · O = 3.44

Is formaldehyde polar or nonpolar, and why?

  1. Nonpolar: it is trigonal planar with no lone pair on carbon, so the three arrows cancel
  2. Polar: the lone pairs on oxygen bend the molecule
  3. Polar: its C=O bond is polar, and a polar bond always makes a polar molecule
  4. Polar: H and O are not identical outer atoms, so the arrows cannot cancel
Dr. Karmach

Practice 7 answer: D

CH₂O: 4 + 2(1) + 6 = 12 valence e⁻
C–H, C–H and C=O use 8 · 12 − 8 = 4 left = 2 lone pairs on O · none on C · trigonal planar
outer atoms H, H, O · ΔEN(C=O) = 0.89 · ΔEN(C–H) = 0.35 → unbalanced: polar → answer D

A stopped at the shape; trigonal planar cancels only when all three outer atoms are identical, as in BCl₃. B let the outer atom's lone pairs set the shape; only lone pairs on the central atom do, and carbon has none. C has the right verdict for a wrong reason: CO₂ has polar bonds and is nonpolar.

Same shape as BCl₃, opposite answer: the strong C=O arrow has no equal partner. ✓
Dr. Karmach

Practice 8

I HCN · II SiCl₄ · III NCl₃
electronegativity: H = 2.20 · C = 2.55 · N = 3.04 · Si = 1.90 · Cl = 3.16

Which of these molecules are polar?

  1. I only
  2. I and III
  3. I and II
  4. III only
Dr. Karmach

Practice 8 answer: B

polar: I HCN and III NCl₃ → answer B
HCN: linear, H and N differ · SiCl₄: tetrahedral, four identical Cl · NCl₃: 5 + 3(7) = 26, 26 − 24 = 2 left: one lone pair on N, pyramidal
ΔEN: C≡N 3.04 − 2.55 = 0.49 · Si–Cl 3.16 − 1.90 = 1.26 · N–Cl 3.16 − 3.04 = 0.12

A skipped the lone-pair question for NCl₃: 0.12 is under 0.4, but the lone pair on nitrogen makes the molecule pyramidal and polar anyway. C judged by the bonds alone: SiCl₄ has the most polar bonds in the set, 1.26, yet its four identical arrows cancel. D read HCN as symmetric like CO₂; a linear shape cancels only when both outer atoms are identical.

The most polar bonds sit in the one nonpolar molecule. The shape decides. ✓
Dr. Karmach

Check yourself

  1. BeCl₂ has two polar Be–Cl bonds in a linear shape, with no lone pair on beryllium. Polar or nonpolar? Give the reason.
  2. A molecule is built from polar bonds yet turns out nonpolar. What must be true about its shape and its outer atoms?

Polar or nonpolar is now a two-step call: name the shape, then add the arrows. Polarity also decides what mixes: polar water dissolves polar substances and leaves nonpolar oil apart. That rule, like dissolves like, returns with liquids and solutions.

Dr. Karmach

Can you…?

  • ☐ classify a compound's bonding as ionic, covalent, or both, and a bond as nonpolar covalent, polar covalent, or ionic from the electronegativity difference?
  • ☐ write Lewis symbols for atoms and ions and show the electron transfer that gives an ionic compound its formula?
  • ☐ draw Lewis structures for molecules and polyatomic ions, including multiple bonds, resonance forms, and the common octet exceptions?
  • ☐ use VSEPR to predict the shape and bond angle of a molecule with up to four electron domains?
  • ☐ combine bond polarity with shape to decide whether a molecule is polar?

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

Dr. Karmach

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