14 entries

Common Organic Functional Groups

The essential organic functional groups with their general formulas, naming conventions, and representative examples. Fundamental to understanding organic chemistry nomenclature.

Functional Group General Formula IUPAC Suffix/Prefix Example Formula
AlkaneCₙH2+2-aneEthaneC2H6
AlkeneCₙH2-eneEthene (ethylene)C2H4
AlkyneCₙH2-2-yneEthyne (acetylene)C2H2
AlcoholR–OH-olEthanolC2H5OH
AldehydeR–CHO-alEthanal (acetaldehyde)CH3CHO
KetoneR–CO–R'-onePropanone (acetone)CH3COCH3
Carboxylic acidR–COOH-oic acidEthanoic acid (acetic acid)CH3COOH
EsterR–COO–R'-oateEthyl ethanoateCH3COOC2H5
AmineR–NH2-amineMethylamineCH3NH2
AmideR–CONH2-amideEthanamide (acetamide)CH3CONH2
EtherR–O–R'prefix: alkoxy-Diethyl etherC2H5OC2H5
HaloalkaneR–X (X = F, Cl, Br, I)prefix: halo-ChloromethaneCH3Cl
ThiolR–SH-thiolEthanethiolC2H5SH
NitrileR–C≡N-nitrileEthanenitrile (acetonitrile)CH3CN

Important Notes

  • R represents any alkyl group (hydrocarbon chain). R' represents a second, possibly different alkyl group.
  • IUPAC priority order (highest to lowest): carboxylic acid > ester > amide > aldehyde > ketone > alcohol > amine > alkene > alkyne > alkane.
  • The highest-priority group determines the suffix; lower-priority groups are named as prefixes.
  • Aldehydes always occur at the end of a carbon chain (terminal); ketones occur within the chain (internal).
  • Common names are shown in parentheses. IUPAC names should be used for formal nomenclature.
  • Naming follows IUPAC 2013 Recommendations for the Nomenclature of Organic Chemistry.