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Topic: Alpha-hydrogen acidity, aldol, Cannizzaro, haloform· Organic Compounds Containing Oxygen

The correct statement regarding a carbonyl compound with a hydrogen atom on its alpha-carbon, is :

1. a carbonyl compound with a hydrogen atom on its alpha-carbon never equilibrates with its corresponding enol.

2. a carbonyl compound with a hydrogen atom on its alpha-carbon rapidly equilibrates with its corresponding enol and this process is known as aldehyde-ketone equilibration.

3. a carbonyl compound with a hydrogen atom on its alpha-carbon rapidly equilibrates with its corresponding enol and this process is known as carbonylation.

4. a carbonyl compound with a hydrogen atom on its alpha-carbon rapidly equilibrates with its corresponding enol and this process is known as keto-enol tautomerism.

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Answer: 4. a carbonyl compound with a hydrogen atom on its alpha-carbon rapidly equilibrates with its corresponding enol and this process is known as keto-enol tautomerism.

Key idea: a carbonyl compound with an alpha hydrogen is in rapid equilibrium with its enol form. This is called keto-enol tautomerism.

The alpha H shifts to oxygen and a C=C forms: \(\mathrm{H-C-C=O \rightleftharpoons C=C-OH}\). Options 2 and 3 name the process wrongly (aldehyde-ketone equilibration and carbonylation are not terms for this), and option 1 is wrong since equilibration does occur.

Doubtly AI · 30 Oct 2026 AI-generated · not yet verified Report
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