3.2.2—Functional groups

Syllabus
First assessment 2025
Objective
3.2.2
Level
HL

Organic Functional Groups

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.

Identifying Functional Groups

Assessment in practice

Representative question

Question 1

[Maximum number: 2]

State the structural formula, functional group name and homologous series of the CHO functional group.

Structural formula drawingFunctional group nameHomologous series name

Organic Analysis Summary

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.