Sharing electrons: how covalent bonds form, what shapes molecules take, and why some molecules are polar and stick together.
This is the Higher Level lesson. The core S2.2.1–S2.2.10 (bonds, VSEPR, polarity, forces, networks) is shared with SL; the HL-only content — sigma & pi bonds, resonance, formal charge and VSEPR for 5–6 electron domains — carries a purple HL badge.
A covalent bond is the electrostatic attraction between a shared pair of electrons and the two nuclei. Atoms share to reach a full outer shell (the octet rule). Sharing more pairs gives double and triple bonds — which are shorter and stronger. A coordinate (dative) bond is a covalent bond where both shared electrons come from the same atom.
| Bond | Shared pairs | Example | Length | Strength |
|---|---|---|---|---|
| Single C–C | 1 | ethane | longest | weakest |
| Double C=C | 2 | ethene | shorter | stronger |
| Triple C≡C | 3 | ethyne | shortest | strongest |
More shared pairs pull the nuclei closer, so as bond order rises the bond gets shorter and stronger.
The VSEPR model says electron domains (bonding pairs and lone pairs) around a central atom repel and spread out as far as possible. Lone pairs repel a little more strongly, squeezing bond angles slightly. Pick a molecule:
Electronegativity is how strongly an atom pulls the shared electrons. If the two atoms differ, the bond is polar — the more electronegative atom gets a partial negative charge (δ−), the other δ+. Whether the whole molecule is polar depends on the shape: if equal bond dipoles point in opposite directions, they cancel.
Covalent bonds are strong, but separate molecules are held to each other by weaker intermolecular forces. These decide melting/boiling points. Click each type:
Some substances aren't made of small molecules at all: covalent network solids like diamond and silicon dioxide are giant lattices of atoms held entirely by strong covalent bonds — so they have very high melting points and are hard. Graphite is a network too, but its layers slide (soft, a lubricant) and its delocalised electrons let it conduct.
Every covalent bond is one of two types. A sigma (σ) bond forms from head-on overlap of orbitals along the bond axis — strong, and free to rotate. A pi (π) bond forms from sideways overlap of p orbitals above and below the axis. The rule: a single bond is 1 σ; a double bond is 1 σ + 1 π; a triple bond is 1 σ + 2 π.
At HL the VSEPR model extends to five and six domains — and to shapes where some domains are lone pairs. Explore:
Sometimes one Lewis structure isn't enough. In ozone (O₃) the two oxygen–oxygen bonds are actually identical, midway between a single and a double bond. We draw two resonance structures linked by a double-headed arrow; the real molecule is a delocalised average of them. Benzene (C₆H₆) is the classic case — six delocalised π electrons spread evenly, drawn as a ring.
Formal charge helps choose the best Lewis structure. For each atom: FC = (valence electrons) − (non-bonding electrons) − ½(bonding electrons). The most likely structure is the one where formal charges are closest to zero. For example, the central O in ozone has FC = 6 − 2 − ½(6) = +1.
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