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Q.a) How does methanal reacts with hydroxylamine? Explain with equation.

(2)
b) Identify A and B in the following reaction.
(2)
H3C−C∥O−CH3+H2N−NH2→−H2OA→HeatKOH/ethylene glycolB+N2↑\text{H}_3\text{C}-\overset{\text{O}}{\overset{\|}{\text{C}}}-\text{CH}_3 + \text{H}_2\text{N}-\text{NH}_2 \xrightarrow{-\text{H}_2\text{O}} \text{A} \xrightarrow[\text{Heat}]{\text{KOH/ethylene glycol}} \text{B} + \text{N}_2 \uparrow
c) Write any one reagent used to distinguish between aldehyde and ketone. (1)
Karnataka PUCKarnataka II PUC Board 2024Subjective· 5mImportance★★★★★
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Methanal + hydroxylamine gives formaldoxime; the scheme is Wolff–Kishner reduction of acetone (A = hydrazone, B = propane); aldehydes and ketones are distinguished with Tollens'/Fehling's reagent.

a) Methanal with hydroxylamine — nucleophilic addition–elimination giving an oxime:

H2C=O+H2N-OH→H2C=N-OH+H2O\text{H}_2\text{C=O} + \text{H}_2\text{N-OH} \rightarrow \text{H}_2\text{C=N-OH} + \text{H}_2\text{O}

(product = formaldoxime / methanal oxime)

b) Identify A and B (Wolff–Kishner reduction of acetone)

Acetone first reacts with hydrazine to form the hydrazone (A); the hydrazone on heating with KOH in ethylene glycol loses N2\text{N}_2 and is reduced to the alkane (B).

(CH3)2C=O+H2N-NH2→−H2O(CH3)2C=N-NH2⏟A(\text{CH}_3)_2\text{C=O} + \text{H}_2\text{N-NH}_2 \xrightarrow{-\text{H}_2\text{O}} \underbrace{(\text{CH}_3)_2\text{C=N-NH}_2}_{A}

(CH3)2C=N-NH2→HeatKOH/ethylene glycolCH3-CH2-CH3⏟B+N2↑(\text{CH}_3)_2\text{C=N-NH}_2 \xrightarrow[\text{Heat}]{\text{KOH/ethylene glycol}} \underbrace{\text{CH}_3\text{-CH}_2\text{-CH}_3}_{B} + \text{N}_2\uparrow

A = acetone hydrazone (CH3)2C=N-NH2(\text{CH}_3)_2\text{C=N-NH}_2; B = propane CH3CH2CH3\text{CH}_3\text{CH}_2\text{CH}_3. …

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