• Covalent bonds result from the overlap of atomic orbitals. A sigma bond (σ) is formed by the direct head-on/end-to-end overlap of atomic orbitals, resulting in electron density concentrated between the nuclei of the bonding atoms. A pi bond (π) is formed by the sideways overlap of atomic orbitals, resulting in electron density above and below the plane of the nuclei of the bonding atoms.

• Formal charge (FC) can be used to decide which Lewis (electron dot) structure is preferred from several. The FC is the charge an atom would have if all atoms in the molecule had the same electronegativity. FC = (Number of valence electrons)-½(Number of bonding electrons)-(Number of non-bonding electrons). The Lewis (electron dot) structure with the atoms having FC values closest to zero is preferred.

• Exceptions to the octet rule include some species having incomplete octets and expanded octets.

• Delocalization involves electrons that are shared by/between more than one pair in a molecule or ion as opposed to being localized between a pair of atoms.

• Resonance involves using two or more Lewis (electron dot) structures to represent a particular molecule or ion. A resonance structure is one of two or more alternative Lewis (electron dot) structures for a molecule or ion that cannot be described fully with one Lewis (electron dot) structure alone.

• Prediction whether sigma (σ) or pi (π) bonds are formed from the linear combination of atomic orbitals.

• Deduction of the Lewis (electron dot) structures of molecules and ions showing all valence electrons for up to six electron pairs on each atom.

• Application of FC to ascertain which Lewis (electron dot) structure is preferred from different Lewis (electron dot) structures.

• Deduction using VSEPR theory of the electron domain geometry and molecular geometry with five and six electron domains and associated bond angles.

• Explanation of the wavelength of light required to dissociate oxygen and ozone.

• Description of the mechanism of the catalysis of ozone depletion when catalysed by CFCs and NOx.

• The linear combination of atomic orbitals to form molecular orbitals should be covered in the context of the formation of sigma (σ) and pi (π) bonds.

• Molecular polarities of geometries corresponding to five and six electron domains should also be covered.