CUET · CHEMISTRY · PYQ PAPER 2025
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Alcohols are versatile compounds as they can act as both nucleophile and electrophile. They undergo reactions based on cleavage of \(\mathrm{O}-\mathrm{H}\) and \(\mathrm{C}-\mathrm{O}\) bonds. The cleavage of \(\mathrm{O}-\mathrm{H}\) bond reflects the acidic character of alcohols. However they are weaker acids than water, phenol and carboxylic acids. Alkoxide ion formed by loss of proton from the OH group of alcohols reacts with water to form the corresponding conjugate acid - base pair. They act as Bronsted base due to presence of unshared electron pairs on oxygen.Both alcohols and phenol react with carboxylic acids, acid chlorides and anhydrides to form esters. The introduction of acetyl group in alcohols or phenol is known as acetylation. Alcohols react with hydrogen halides to form alkyl halides which form the basis of Lucas test. They also undergo acid catalyzed dehydration to form alkenes. Alcohols can be easily oxidized with variety of oxidizing agents. The nature of the product depends on the type of oxidizing agent and the nature of alcohol.
Oxidation of alcohols involves formation of carbon oxygen double bond with
- A Cleavage of an O-H bond
- B Cleavage of C-H bond
- C Cleavage of of O-H bond and C-H bond
- D Cleavage of C-C bond
Answer & Solution
Correct Answer
(C) Cleavage of of O-H bond and C-H bond
Step-by-step Solution
Detailed explanation
Cleavage of of O-H bond and C-H bond
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