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3 Functional group reference

Every organic question starts with recognising the functional group. Learn this table cold, the suffix/prefix drives naming, and the group drives the reactions. Watch: Functional group reference Opens a YouTube search: pick a video that clicks for you
Level 3 functional groups
ClassGroupExample (condensed)Suffix / prefix
AlkaneC–C onlyCH₃CH₃ ethane-ane
AlkeneC=CCH₂=CH₂ ethene-ene
HaloalkaneC–X (F,Cl,Br,I)CH₃CH₂Br bromoethanehalo- prefix
Alcohol–OHCH₃CH₂OH ethanol-ol
Aldehyde–CHO (end)CH₃CHO ethanal-al
KetoneC=O (middle)CH₃COCH₃ propanone-one
Carboxylic acid–COOHCH₃COOH ethanoic acid-oic acid
Ester–COO–CH₃COOCH₃ methyl ethanoate-yl -oate
Amine–NH₂CH₃CH₂NH₂ ethylamine-amine / amino-
Amide–CONH₂CH₃CONH₂ ethanamide-amide
Nitrile–C≡NCH₃CN ethanenitrile-nitrile
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Mnemonic: suffix priority order

“All Excellent Alchemists Need A Keen Analytical Approach” → Acid · Ester · Amide · Nitrile · Aldehyde · Ketone · Alcohol · Amine. (Alkene/alkyne and halogens never win: they’re always prefixes or the parent chain.)

Naming priority (which group gets the suffix)

  • Priority order (highest first): carboxylic acid > ester > amide > nitrile > aldehyde > ketone > alcohol > amine > alkene.
  • The highest-priority group takes the suffix and lowest locant; everything else becomes a prefix (hydroxy-, oxo-, amino-, halo-).
  • Alkene/alkyl chains and halogens are always prefixes or the parent chain.

Practise just this