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A carbonyl compound reacts with hydrogen cyanide to form cyanohydrin, which on hydrolysis, forms a racemic mixture of α-hydroxy acid. The carbonyl compound is:

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Important Questions on Carbonyl Compounds

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Compound (A) C5H10O forms a phenylhydrazone and gives negative Tollens and iodoform tests. Compound (A) on reduction, gives n-pentane. Compound (A) is:
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The most reactive compound towards the formation of cyanohydrin on treatment with KCN, followed by acidification is:
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Which of the following statements regarding the chemical properties of acetophenone are wrong?
I. It is reduced to methylphenylcarbinol by sodium and ethanol.
II. It is oxidised to benzoic acid with acidified KMnO4.
III. It does not undergo electrophilic substitution like nitration at the meta-position.
IV. It does not undergo iodoform reaction with iodine and alkali.