Cyclohexanecarboxylic acid

The carboxyl group has a conformational energy slightly lower than that of the methyl group. Let's try to understand why.

Chair equilibrium of cyclohexanecarboxylic acid: the planar carboxyl group barely interacts with the axial hydrogens at 3 and 5
equatorial
cyclohexanecarboxylic
Acid
Axial
cyclohexanocarboxylic
acid

The carboxyl group is planar because of the C=O bond and its sp2 hybridization. By the rotation of the C-C bond -curved arrow-, the planar carboxyl can always find an arrangement where its interaction with the ring's axial hydrogens at positions 3 and 5 is lower than that of a methyl group.

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