Carboxylic acids
Aldehydes
Structure
Trivial name
IUPAC name
Structure
Trivial name
IUPAC name
H - COOH
Formic acid
Methanoic acid
H-CHO
Formaldehyde
Methanal
CH
- COOH 3
Acetic acid
Ethanoic acid
CH
-CHO 3
Acetaldehyde
Ethanal
CH
- CH 3
- COOH 2
Propionic acid
Propanoic acid
CH
-CH 3
-CHO 2
Propionaldehyde
Propanal
CH
- CH 3
- CH 2
- COOH 2
n-Butyric acid
Butanoic acid
CH
-CH 3
-CH 2
-CHO 2
Butyraldehyde
Butanal
(CH
) 32
CH - COOH
Isobutyric acid ( α
- methylpropionic
acid)
2-Methylpropanoic acid
(CH
) 32
CH-CHO
Isobutyrlaldehyde (α
- methylpropionaldehyde)
2 - Methylpropanal
CH
= CH - COOH 2
Acrylic acid
Prop-2-enoic acid
CH
=CH-CHO 2
Acrolein
Prop-2-enal
HOOC - COOH
Oxalic acid
Ethanedioic acid
CHO-CHO
Oxaldehyde (Glyoxal)
Ethanedial
COOH
Benzoic acid (Benzenecarboxylic acid)
Benzoic acid
CHO
Benzaldehyde
Benzaldehyde(Benzenecarbaldehyde)
COOHCH
3
o-Toluic acid
2-Methylbenzoic acid
CHOCH
3
o-Tolualdehyde
2-Methylbenzaldehyde
COOHOH
Salicyclic acid
2-Hydroxybenzoic acid
CHOOH
Salicylaldehyde
2-Hydroxybenzaldehyde
COOHCOOH
Phthalic acid
Benzene-1,2-dicarboxylic acid
CHOCHO
Phthalaldehyde
Benzene-1,2-dicarbaldehyde
COOH
Cyclohexylcarboxylic acid
Cyclohexanecarboxylic acid
CHO
Cyclohexane aldehyde
Cyclohexanecarbaldehyde
Table 12.1 Trivial and IUPAC names of carboxylic acids and aldehydes