3.2.2—Functional groups
- Syllabus
- First assessment 2025
- Objective
- 3.2.2
- Level
- SL
| Family | Complete recognition pattern | Bounded characteristic cue |
|---|---|---|
| Halogenoalkane | C–F/Cl/Br/I | polar C–X bond |
| Alcohol / hydroxyl | C–OH, not the –OH inside –COOH | can donate and accept hydrogen bonds |
| Aldehyde | terminal –CHO carbonyl | polar C=O; terminal carbonyl |
| Ketone | –CO– between carbons | polar C=O; internal carbonyl |
| Carboxylic acid | –COOH | acidic proton and hydrogen bonding |
| Ether / alkoxy | C–O–C | oxygen accepts hydrogen bonds but has no O–H donor |
| Amine / amino | C–N without adjacent carbonyl | basic lone-pair chemistry; N–H species may donate H bonds |
| Amide / amido | –CONH₂/–CONHR/–CONR₂ | nitrogen directly attached to carbonyl |
| Ester | –COO– between carbon groups | carbonyl and single-bond O in one group |
| Phenyl | C₆H₅– attached as a substituent | aromatic ring pattern |
Identify the whole local bonding pattern before naming the group; these cues support classification, not a complete reaction mechanism.
Identify the characteristic atoms and bonding pattern first, then give the functional-group name and relevant property context.
Identify the complete bonding pattern: an aldehyde has a terminal –CHO carbonyl, a ketone has C=O between carbons, and an ester contains –C(=O)–O–. Do not label every O–H as an alcohol or every C–N as an amine without checking the neighbouring carbonyl.
Saturation describes carbon-carbon bonding: a saturated compound has only C-C single bonds, while an unsaturated compound contains at least one C=C or C≡C bond. A carbonyl C=O does not by itself make the carbon skeleton unsaturated. Identify saturation separately from identifying hydroxyl, carbonyl, carboxyl or other functional groups.
Representative question
State the structural formula, functional group name and homologous series of the CHO functional group.
| Structural formula drawing | Functional group name | Homologous series name |
|---|---|---|
isomers
Accept "same molecular formula".
3.
(e)
(ii)
Full structural
formula
Functional group
name
Homologous series
−cO′H
carbonyl
aldehyde
\end{tabular}
structure
carbonyl AND aldehyde
\end{tabular}
Accept R/C attached to functional group in the full structural formula.
Central C must have 4 bonds for M1.
Retrieve the route: translate formulae, identify functional groups and series, name and classify isomers, then use mass, IR, and NMR evidence together to determine structure.
Check connectivity, functional-group evidence, formula/mass constraint, shifts and integration, splitting neighbours, and agreement across every technique.