AP | A-Level | IB | NCERT 11 + 12 – FREE NOTES, RESOURCES AND VIDEOS!
S1.1 - Introduction to the particulate nature of matter S1.2 - The nuclear atom S1.3 - Electron configurations S1.4 - Counting particles by mass - The mole S1.5 - Ideal gases S2.1 - The ionic model S2.2 - The covalent model S2.3 - The metallic model S2.4 - From models to materials S3.1 - The periodic table - Classification of elements S3.2 - Functional groups - Classification of organic compounds R1.1 - Measuring enthalpy changes R1.2 - Energy cycles in reactions R1.3 - Energy from fuels R1.4 - Entropy and spontaneity AHL R2.1 - How much? The amount of chemical change R2.2 - How fast? The rate of chemical change R2.3 - How far? The extent of chemical change R3.1 - Proton transfer reactions R3.2 - Electron transfer reactions R3.3 - Electron sharing reactions R3.4 - Electron-pair sharing reactions

S3.2 - Functional groups - Classification of organic compounds

3.2.1 Representing Organic Compounds 3.2.2 Functional Group 3.2.3 Homologous Series 3.2.4 Trends and Properties of Homologous Series 3.2.5 Nomenclature 3.2.6 Structural Isomerism 3.2.7 Stereoisomerism and Chirality (AHL) 3.2.8 Mass Spectrometry (MS) of Organic Compounds (AHL) 3.2.9 Infrared (IR) Spectroscopy and Greenhouse Gases (AHL) 3.2.10 Proton NMR Spectroscopy (AHL) 3.2.11 Splitting Patterns in Proton NMR Spectroscopy (AHL) 3.2.12 Interpreting Spectra (AHL)

Functional Groups and Organic Classes

Specification Reference S3.2.2

Quick Notes

  • A functional group is a specific group of atoms that determines the chemical and physical properties of a compound.
  • Organic molecules are classified based on the functional group(s) they contain.
  • Important to know both names and structures of the following groups:
    • Halogeno (–X): F, Cl, Br, I
    • Hydroxyl (–OH): alcohols
    • Carbonyl (>C=O): aldehydes and ketones
    • Carboxyl (–COOH): carboxylic acids
    • Alkoxy (–OR): ethers
    • Amino (–NH2): amines
    • Amido (–CONH2): amides
    • Ester (–COOR): esters
    • Phenyl (–C6H5): aromatic ring
  • Saturated = only single C–C bonds
  • Unsaturated = contains at least one C=C double or C≡C triple bond

Full Notes

What Are Functional Groups?

Functional groups are specific atoms or groups of atoms that give distinct chemical reactivity and physical properties to organic molecules.

They define homologous series such as alcohols, carboxylic acids, and esters.

IB Chemistry table of key functional groups including halogeno, hydroxyl, carbonyl, carboxyl, amino, ester, amide and phenyl.
Name Structure Example Found In Notes
Halogeno –X (F, Cl, Br, I) Haloalkanes E.g. CH3Cl
Hydroxyl –OH Alcohols Polar, allows hydrogen bonding
Carbonyl >C=O Aldehydes and Ketones Aldehydes: end of chain, Ketones: middle
Carboxyl –COOH Carboxylic acids Weak acids
Alkoxy –OR Ethers R–O–R′ structure
Amino –NH2 Amines Basic group
Amido –CONH2 Amides Formed in peptide bonds
Ester –COOR Esters Derived from acids and alcohols
Phenyl –C6H5 Aromatic compounds Benzene ring attached as substituent

Saturated vs Unsaturated Compounds

Saturated compounds contain only single bonds between carbon atoms.

Example Ethane

CH3–CH3

Unsaturated compounds contain one or more double (C=C) or triple (C≡C) bonds.

Example Ethene and Ethyne

Ethene → CH2=CH2
Ethyne → HC≡CH

Recognising Functional Groups from Structures

You should be able to:

Linked Course Questions

AHL Structure 2.4 – Linked Course Question

What is the nature of the reaction that occurs when two amino acids form a dipeptide?

When two amino acids react, the amine group (–NH2) of one reacts with the carboxyl group (–COOH) of the other in a condensation reaction. This forms a peptide bond (–CONH–) and releases a molecule of water. The resulting compound is called a dipeptide.


Nature of Science, Reactivity 3.2, 3.4 – Linked Course Question

How can functional group reactivity be used to determine a reaction pathway between compounds?

Understanding how functional groups react allows chemists to plan a reaction pathway — a step-by-step sequence of reactions to convert one compound into another.

For example:

  • Ethene → Ethanol via hydration (addition of water)
  • Ethanol → Ethanoic acid via oxidation

Each step targets a specific functional group transformation (alkene → alcohol → carboxylic acid), showing how functional group reactivity guides synthetic planning.

Summary