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CUET · CHEMISTRY · PYQ PAPER 2025

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The carbonyl group of aldehydes and ketones is highly polar. The positively charged carbon is readily attacked by electron-rich nucleophile and the negatively charged oxygen atom is attacked by an electro-deficient electrophile. Aldehydes and ketones undergo nucleophilic addition reactions in the presence of acid or a base. The mechanism involves attack of a nucleophile on the electron deficient carbonyl carbon to form a tetrahedral intermediate. A new bond is formed between the carbon and oxygen. Protonation of the anion furnished by the reaction medium yields a neutral addition product. The addition product is same whether the reaction is catalyzed by acid or a base. For example in the presence of base aldehydes and ketones react with hydrogen cyanide to form cyanohydrin.
Which of the following reactions is not a nucleophilic addition reaction of aldehydes and ketones?

  1. A Addition of water
  2. B Addition of sodium Hydrogen Sulphite
  3. C Addition of alcohol
  4. D Addition of sodium borohydride
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Answer & Solution

Correct Answer

(C) Addition of alcohol

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Detailed explanation

The formation of acetals from aldehydes/ketones and alcohols is an overall reaction that involves an initial nucleophilic addition (to form a hemiacetal) followed by a dehydration step and a second nucleophilic attack/substitution. This process results in the elimination of a…
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