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Reference—Structural, displayed and skeletal formula conventions

Syllabus
9701–2028–2029
Objective
Level
AS

Draw organic structures unambiguously in the accepted formula conventions

Structural formulae show connectivity, displayed formulae show bonds, skeletal formulae show the carbon framework, and partial-skeletal forms combine conventions. Use enough bonds and labels to make one structure unambiguous.

Show heteroatoms and their attached hydrogens, indicate multiple bonds and use the accepted benzene-ring convention. A condensed formula must still distinguish functional-group position and branching.

CH₃CH(OH)CH₃ identifies propan-2-ol; a skeletal chain with –OH at the middle carbon conveys the same connectivity.

Leaving out a carbon-bound hydrogen is normal in skeletal notation, but leaving out a heteroatom or bond needed to distinguish isomers is not.

ConceptA-Level CAIE Chemistry AS