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
AlkaneCₙH⁠2ₙ⁠+2-aneEthaneC⁠2H⁠6
AlkeneCₙH⁠2-eneEthene (ethylene)C⁠2H⁠4
AlkyneCₙH⁠2ₙ⁠-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.