Gr 11 · Chemistry · Deep Study

Understanding Bonds

Bonds form when atoms achieve lower energy together than apart. This guide covers ionic and covalent bonding, Lewis structures, VSEPR geometry, and polarity — with diagrams at each step.

5 sections Worked examples with steps Checkpoint questions Intuition-first explanations
1
Ionic Bonding
Electron transfer between metals and nonmetals

When a metal atom meets a nonmetal atom, there is a dramatic mismatch in how strongly each holds its electrons. The metal barely grips its outer electrons; the nonmetal desperately wants more. The result is a complete transfer — an electron leaves one atom and joins the other, creating two oppositely charged ions that attract each other strongly.

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Why do metals and nonmetals form ionic bonds?
Metals have low ionization energies — it costs very little energy to remove their outer electrons. Nonmetals have high electron affinities — they release substantial energy when they gain electrons. The combined energy released by the electron transfer is greater than the energy required to remove the electron in the first place, so the ionic compound is lower in energy (more stable) than the separate atoms. Nature always gravitates toward the lower-energy state.
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Key facts:
ΔEN > 1.7 → ionic bond. Cation = metal that lost e⁻ (positively charged). Anion = nonmetal that gained e⁻ (negatively charged). Ions arrange into a crystal lattice for maximum electrostatic stability.
Na 11 e⁻ 1 Ve⁻ e⁻ transfer Cl 17 e⁻ Na⁺ 10 e⁻ Cl⁻ 18 e⁻ electrostatic attraction Crystal lattice + + + + + Na⁺/Cl⁻ alternating
Electron transfer from Na to Cl → ions form → arrange into crystal lattice
★ Easy
Classifying NaCl as ionic
Na has EN = 0.93; Cl has EN = 3.16. Explain why NaCl is ionic and identify the ions formed.
Show solution
1
Calculate ΔEN
ΔEN = 3.16 − 0.93 = 2.23
2
Apply threshold rule

ΔEN = 2.23 > 1.7 → ionic bond. The difference is large enough that Cl essentially takes Na's electron rather than sharing it.

3
Identify ions
Na (Group 1) loses 1 e⁻ → Na⁺ (cation)
Cl (Group 17) gains 1 e⁻ → Cl⁻ (anion)

Both ions now have 8 valence electrons (full octet). Na⁺ matches Ne; Cl⁻ matches Ar.

Answer: ΔEN = 2.23 > 1.7 → ionic. Na⁺ and Cl⁻ form by electron transfer.
★★ Intermediate
Comparing lattice strength: NaCl vs MgO
MgO has a melting point of 2852 °C; NaCl melts at 801 °C. Explain the difference in terms of ionic bonding.
Show solution
1
Identify the ions in each compound
NaCl: Na⁺ (charge 1+) and Cl⁻ (charge 1−)
MgO: Mg²⁺ (charge 2+) and O²⁻ (charge 2−)
2
Apply Coulomb's law logic

Electrostatic force is proportional to the product of the charges. For MgO: (2+)(2−) = 4 times the charge product of NaCl: (1+)(1−) = 1. The lattice forces in MgO are roughly 4× stronger.

3
Ion size also plays a role

Mg²⁺ is smaller than Na⁺ (higher charge pulls electrons closer), and O²⁻ is smaller than Cl⁻. Smaller ions get closer together, further increasing lattice energy.

Answer: MgO has 2+ and 2− ions vs 1+ and 1− in NaCl. Higher charges → much stronger lattice → far higher melting point.
Checkpoint 1
a) Classify CaF₂ as ionic or covalent and explain using electronegativity. (Ca EN = 1.00; F EN = 3.98)
b) Which compound has a higher melting point: NaCl or MgO? Why?
c) Why do ionic compounds conduct electricity when dissolved in water but not as solids?

a) ΔEN = 3.98 − 1.00 = 2.98 > 1.7 → ionic. Ca loses 2 electrons (one to each F), forming Ca²⁺ and 2 F⁻.

b) MgO has a higher melting point. Mg²⁺ and O²⁻ have double the charge of Na⁺ and Cl⁻, creating much stronger electrostatic attraction in the lattice. Higher lattice energy = more energy required to break → higher melting point.

c) In a solid, all ions are locked in fixed positions in the lattice and cannot move — so no charge flows. When dissolved in water (or melted), the ions are free to move independently and carry electrical current. Conductivity requires mobile charge carriers.

2
Covalent Bonding
Electron sharing between nonmetals — single, double, and triple bonds

When two nonmetal atoms approach each other, neither is willing to give up electrons completely — both have relatively high electronegativities. Instead, they reach a compromise: they share electron pairs. Each shared pair is attracted by both nuclei simultaneously, holding the atoms together.

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Why do two nonmetals share instead of transfer?
Consider two chlorine atoms (Cl–Cl). Both have EN = 3.16. Neither can pull electrons away from the other because the pull is identical. So instead of a winner and a loser, both atoms share equally — the electrons spend time between both nuclei, attracting both simultaneously. This shared pair is the covalent bond, and it is lower in energy than two separate Cl atoms.
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Bond order: single bond = 1 shared pair (2 e⁻); double bond = 2 shared pairs (4 e⁻); triple bond = 3 shared pairs (6 e⁻).
More bonds = shorter bond length and higher bond energy. ΔEN < 1.7 → covalent.
H₂ — Single Bond H H 2 shared e⁻ 432 kJ/mol bond energy O₂ — Double Bond O O 4 shared e⁻ 498 kJ/mol bond energy N₂ — Triple Bond N N 6 shared e⁻ 945 kJ/mol (strongest) bond energy
Single, double, and triple covalent bonds — more shared pairs = shorter bond and higher bond energy
★ Easy
H₂O — counting bonds and lone pairs
Describe the covalent bonding in H₂O. How many bonds does O form? Does O have a full octet?
Show solution
1
Determine valence electrons
O (Group 16): 6 valence e⁻
H (Group 1): 1 valence e⁻ each
2
Form bonds (H needs a duet; O needs an octet)

O forms 2 single bonds — one with each H. Each bond uses 1 e⁻ from O and 1 e⁻ from H = 2 shared e⁻.

3
Count electrons around O
2 bonding pairs (4 e⁻) + 2 lone pairs (4 e⁻) = 8 e⁻ → full octet

Each H has 2 electrons (duet complete). O has 8 electrons (octet complete).

Answer: O forms 2 single bonds, has 2 lone pairs. O has a full octet (8 e⁻). Each H has a duet (2 e⁻).
★★ Intermediate
CO₂ — double bonds explained
Show why CO₂ requires double bonds. Account for all 16 valence electrons and verify each atom's octet.
Show solution
1
Count total valence electrons
C (Group 14): 4 Ve⁻
O × 2 (Group 16): 2 × 6 = 12 Ve⁻
Total: 4 + 12 = 16 Ve⁻
2
Try single bonds first (O−C−O)
2 single bonds use 4 e⁻. Remaining: 12 e⁻
Fill outer O octets (6 e⁻ each): 12 e⁻ used. Remaining: 0
But C now has only 4 e⁻ (the 2 single bonds) — not 8! C needs an octet.
3
Form double bonds to complete C's octet
Convert 1 lone pair on each O into a second bonding pair with C.
Result: O=C=O (two double bonds)

Now check: C has 4+4=8 e⁻ (two double bonds × 2 pairs each = 8). Each O has 4 bonding + 4 lone = 8. Total = 16 ✓

Answer: O=C=O. C has two double bonds (8 e⁻). Each O has one double bond + 2 lone pairs (8 e⁻). All 16 e⁻ accounted for.
Checkpoint 2
a) How many covalent bonds does N (5 valence e⁻) typically form? Why?
b) Which bond is shorter: C−O (single) or C=O (double)? Why?
c) Why does N₂ have a triple bond rather than a single or double bond?

a) N has 5 valence electrons. It needs 3 more to reach an octet, so it forms 3 covalent bonds (with 1 lone pair remaining). Example: NH₃ has 3 N−H bonds.

b) C=O (double bond) is shorter. More shared electron pairs pull the atoms closer together. Double bonds always have shorter bond lengths than the equivalent single bond.

c) N has 5 valence electrons — it needs 3 bonds to complete its octet. Two N atoms each contribute 3 electrons to bonding, forming 3 shared pairs = a triple bond. The triple bond also gives N₂ extremely high bond energy (945 kJ/mol), making it very stable and chemically unreactive.

3
Lewis Structures
Mapping every valence electron in a molecule

A Lewis structure is a complete map of all valence electrons in a molecule — both the bonding pairs connecting atoms and the lone pairs sitting on individual atoms. Mastering Lewis structures is the key to understanding shape, polarity, and reactivity.

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Why do Lewis structures matter?
Lewis structures show every valence electron — bonding pairs and lone pairs. They predict shape (via VSEPR), polarity, reactivity, and even how molecules react. A lone pair on nitrogen is what makes NH₃ a base — it donates that pair to an H⁺. You cannot understand chemistry without understanding where the electrons are.
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5 steps: (1) count total Ve⁻, (2) skeleton with least EN in centre, (3) octets on outer atoms, (4) remaining e⁻ on central atom, (5) form multiple bonds if central atom needs more e⁻.
Step 1: Count Ve⁻ O: 6 Ve⁻ H × 2: 2 Ve⁻ Total = 8 Ve⁻ Step 2: Skeleton H O H O in centre (least EN? No — O must be centre) Step 3: Fill outer atoms H O H H needs duet — done! 4 e⁻ used. 4 remain. Step 4: Lone pairs H O H 2 lone pairs on O All 8 e⁻ placed ✓
Lewis structure of H₂O — step by step. Total 8 valence electrons: 4 in bonds, 4 as 2 lone pairs on O.
★ Easy
Lewis structure of NH₃
Draw the Lewis structure of NH₃ using the 5-step method.
Show solution
1
Count total valence electrons
N: 5 Ve⁻ + 3 × H (1 Ve⁻ each) = 5 + 3 = 8 Ve⁻
2
Skeleton — N in centre (less EN than… wait, H can't be centre)

N is the central atom. Three H atoms surround it.

3
Fill outer atoms — H only needs a duet
3 N−H bonds = 3 × 2 = 6 e⁻ used. Remaining: 8 − 6 = 2 e⁻
4
Place remaining electrons on central atom
2 e⁻ → 1 lone pair on N

Check N: 3 bonding pairs (6 e⁻) + 1 lone pair (2 e⁻) = 8 e⁻ → full octet.

5
Multiple bonds needed?

No — N already has a complete octet. Structure is final: N with 3 single bonds to H and 1 lone pair.

Answer: NH₃ has 3 N−H single bonds and 1 lone pair on N. All atoms have complete shells. Total 8 Ve⁻ placed.
★★ Intermediate
Lewis structure of CO₂
Draw the Lewis structure of CO₂ showing why double bonds form. Verify with formal charges.
Show solution
1
Count total valence electrons
C: 4 Ve⁻ + 2 × O: 2 × 6 = 12. Total = 16 Ve⁻
2–3
Skeleton + fill outer O with single bonds first
O−C−O: 2 single bonds = 4 e⁻. Remaining: 12 e⁻
Fill each O with 3 lone pairs (6 e⁻ each): 12 e⁻ used. Remaining: 0

But C only has 2 bonding pairs = 4 e⁻. C needs 8 e⁻! Must form multiple bonds.

4
Convert lone pairs → double bonds
Move 1 lone pair from each O into a bonding pair with C.
Result: O=C=O

C: 2 double bonds = 8 e⁻ (octet ✓). Each O: 1 double bond + 2 lone pairs = 4 + 4 = 8 e⁻ (octet ✓). Total e⁻ = 16 ✓

5
Verify formal charges
C: FC = 4 − 0 − ½(8) = 4 − 4 = 0
O: FC = 6 − 4 − ½(4) = 6 − 4 − 2 = 0

All formal charges = 0 → this is the best Lewis structure.

Answer: O=C=O. Two double bonds. C and both O all have formal charge = 0. Total 16 Ve⁻ placed.
Checkpoint 3
a) Draw the Lewis structure for HCl. How many lone pairs does Cl have?
b) Draw the Lewis structure for O₂. (Hint: it needs a double bond.)
c) How do you know when to form a multiple bond in a Lewis structure?

a) HCl: H−Cl with 3 lone pairs on Cl. Total Ve⁻ = 1 + 7 = 8. Bond uses 2 e⁻; 6 remaining go as 3 lone pairs on Cl. H has duet; Cl has octet.

b) O₂: Total Ve⁻ = 6 + 6 = 12. If single bond: O−O, fill each O with 3 LP = 12 e⁻ used; each O has 2 + 6 = 8. But wait — with single bond + 3LP each: 2 + 12 = 14 e⁻ needed for 12 available. Move 1 LP from each O → shared pair → O=O double bond + 2 LP on each O. Total: 4 bond + 8 lone = 12 ✓. Each O: 4 bond + 4 lone = 8 ✓.

c) Form a multiple bond when: after completing outer atoms' octets and placing all remaining e⁻ on the central atom, the central atom still does not have 8 electrons. Convert a lone pair from an outer atom into a second bonding pair shared with the central atom. Repeat until the central atom has a full octet.

4
VSEPR Geometry
Electron repulsion determines the shape of every molecule

Once you have a Lewis structure, VSEPR lets you predict the three-dimensional shape. The key insight is simple: electron groups around the central atom repel each other and spread as far apart as possible, minimizing the repulsion energy.

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Why do lone pairs compress bond angles?
Lone pairs are not constrained between two nuclei like bonding pairs are. A bonding pair is held in a relatively narrow region between two positive nuclei. A lone pair sits on just one nucleus and spreads out more, taking up more angular space. This extra volume means lone pairs push bonding pairs closer together. One lone pair compresses angles from 109.5° to ~107° (NH₃); two lone pairs compress further to ~104.5° (H₂O).
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Count all electron groups first (bonding pairs + lone pairs). Then read off the shape from the table. Double and triple bonds count as ONE electron group.
Linear CO₂ · 180° O C O 180° Trig. Planar BF₃ · 120° B F F F 120° Tetrahedral CH₄ · 109.5° C H H H H 109.5° Trig. Pyramidal NH₃ · 107° N LP H H H ~107° Bent H₂O · 104.5° O 2 LP H H ~104.5° Angle decreases: 2 lone pairs (H₂O) compress more than 1 lone pair (NH₃) which compresses more than 0 (CH₄)
The five key molecular geometries from VSEPR — lone pairs progressively compress bond angles
★ Easy
Predicting the shape of CH₄
Predict the molecular geometry and bond angle of CH₄ using VSEPR.
Show solution
1
Write the Lewis structure
C (4 Ve⁻) + 4×H (1 Ve⁻) = 8 Ve⁻
4 C−H single bonds, 0 lone pairs on C
2
Count electron groups around central atom C
4 bonding pairs + 0 lone pairs = 4 electron groups
3
Read from VSEPR table

4 electron groups, 0 lone pairs → tetrahedral geometry → bond angle 109.5°

Answer: Tetrahedral geometry, bond angle 109.5°. No lone pairs, so ideal angle is maintained.
★★ Intermediate
H₂O — why bent, not tetrahedral
H₂O has 4 electron groups around O, yet is described as "bent." Explain the difference between electron geometry and molecular shape.
Show solution
1
Lewis structure: electron groups
O has 2 bonding pairs (2 O−H bonds) + 2 lone pairs = 4 electron groups total
2
Electron geometry (all groups)

4 electron groups → electron geometry is tetrahedral. This describes where all four electron groups point.

3
Molecular shape (atoms only)

Molecular shape only considers atom positions (O and 2 H). The 2 lone pairs are invisible. With only 2 bonding pairs and 2 lone pairs, the molecular shape is bent.

4
Effect of lone pairs on bond angle
Ideal tetrahedral = 109.5°
2 lone pairs compress the H−O−H angle to ~104.5°

NH₃ has only 1 lone pair → 107°. H₂O has 2 → 104.5°. Each lone pair compresses further.

Answer: Electron geometry = tetrahedral (4 e⁻ groups). Molecular shape = bent (only atoms counted). Bond angle = 104.5° (2 LP compress it from 109.5°).
Checkpoint 4
a) Predict the molecular geometry and bond angle of NH₃.
b) Predict the molecular geometry of CO₂. (Hint: count electron groups on C.)
c) Why is the bond angle in H₂O (104.5°) less than in NH₃ (107°)?

a) NH₃: N has 3 bonding pairs + 1 lone pair = 4 electron groups. Electron geometry = tetrahedral. Molecular shape = trigonal pyramidal (1 LP, 3 bonding pairs). Bond angle ≈ 107°.

b) CO₂: C has 2 double bonds (each double bond = 1 electron group) + 0 lone pairs = 2 electron groups. VSEPR: 2 groups → linear. Bond angle = 180°.

c) H₂O has 2 lone pairs around O; NH₃ has only 1 lone pair around N. Each lone pair takes up more angular space than a bonding pair and pushes the bonding pairs closer together. The second lone pair in H₂O adds extra compression beyond what 1 lone pair does in NH₃, resulting in 104.5° vs 107°.

5
Polarity
Why shape determines whether a molecule is polar or nonpolar

Polarity operates at two levels: bond polarity (does a single bond have an uneven electron distribution?) and molecular polarity (does the whole molecule have a net dipole?). These are related but not the same — you must consider both electronegativity difference and molecular shape.

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Why can a molecule with polar bonds be nonpolar overall?
Think of a tug-of-war. In CO₂, two oxygen atoms each pull on carbon with equal force in exactly opposite directions. The pulls cancel — net force on carbon is zero. Similarly, the bond dipoles of the two C=O bonds point in opposite directions and cancel, giving CO₂ a net dipole of zero. In H₂O, the two O−H dipoles both point in roughly the same direction (toward the O, due to the bent shape) and add together, giving a net dipole that makes water polar.
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Rule: polar bonds + asymmetric shape → polar molecule. Polar bonds + symmetric shape → nonpolar molecule.
ΔEN < 0.5 = nonpolar covalent; 0.5–1.7 = polar covalent; > 1.7 = ionic.
CO₂ — Linear, Nonpolar O C O δ→ C C ←δ Dipoles cancel → net dipole = 0 → NONPOLAR μ = 0 D H₂O — Bent, Polar O H H net dipole → Dipoles add → net dipole ≠ 0 → POLAR μ = 1.85 D
CO₂: linear shape causes polar bond dipoles to exactly cancel → nonpolar. H₂O: bent shape causes dipoles to add → polar.
★ Easy
HCl — polar bond, polar molecule
Determine whether HCl is polar. (H EN = 2.20; Cl EN = 3.16)
Show solution
1
Calculate ΔEN
ΔEN = 3.16 − 2.20 = 0.96

0.5 < 0.96 < 1.7 → polar covalent bond. Cl is δ− and H is δ+.

2
Assess molecular polarity

HCl is a diatomic molecule — only one bond. There is nothing to cancel with. The bond dipole IS the molecular dipole.

Answer: HCl is polar covalent (ΔEN = 0.96). H is δ+ and Cl is δ−. The molecule is polar since there is only one bond — it cannot cancel.
★★ Intermediate
CCl₄ vs CHCl₃ — symmetry makes the difference
Explain why CCl₄ is nonpolar but CHCl₃ is polar, even though both have tetrahedral geometry.
Show solution
1
CCl₄: 4 identical polar C−Cl bonds
ΔEN(C−Cl) = 3.16 − 2.55 = 0.61 → polar bonds

Tetrahedral shape with 4 identical substituents is perfectly symmetric. The 4 C−Cl dipoles point toward each Cl at tetrahedral angles — they cancel perfectly in 3D. Net dipole = 0 → nonpolar.

2
CHCl₃: 3 C−Cl bonds + 1 C−H bond
ΔEN(C−H) = 2.55 − 2.20 = 0.35 → nearly nonpolar
ΔEN(C−Cl) = 0.61 → polar

The geometry is still tetrahedral. But now one position has H (weak dipole) and three have Cl (stronger dipole). The molecule is no longer symmetric — the 3 C−Cl dipoles all pull in the same general direction (toward the Cl end). They do not cancel. Net dipole ≠ 0 → polar.

Answer: CCl₄: symmetric → dipoles cancel → nonpolar. CHCl₃: asymmetric (H ≠ Cl) → dipoles don't cancel → polar. Same geometry, different symmetry.
Checkpoint 5
a) Is BF₃ polar or nonpolar? It has trigonal planar geometry and all B−F bonds are polar.
b) Is NH₃ polar? It has trigonal pyramidal geometry.
c) Explain why CO₂ is nonpolar even though each C=O bond is polar.

a) BF₃ is nonpolar. Although each B−F bond is polar (F is highly electronegative), the trigonal planar shape is perfectly symmetric: all three B−F dipoles are at 120° to each other and cancel exactly. Net dipole = 0 → nonpolar overall.

b) NH₃ is polar. The three N−H bonds are polar (N is more EN than H). The trigonal pyramidal shape is asymmetric — all three N−H dipoles point in roughly the same direction (toward N, which is on top of the pyramid). They add together rather than cancel. The lone pair on N also contributes to the net dipole. Net dipole ≠ 0 → polar molecule.

c) Each C=O bond is polar because O (EN = 3.44) is more electronegative than C (EN = 2.55), so electron density is shifted toward O. However, CO₂ is linear — the two C=O dipoles point in exactly opposite directions (180° apart) and are equal in magnitude. They cancel completely, giving a net molecular dipole of zero. A molecule can have very polar bonds and still be nonpolar if its shape places those dipoles to cancel.