Question:

Write the product(s) when : (I) One mol of ethanal is treated with 1 mol of \(CH_3OH\) in the presence of dry HCl gas. (II) Benzaldehyde is treated with conc. NaOH. (III) Ethanoic acid is heated in the presence of \(P_2O_5\).

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One mole of alcohol reacts with an aldehyde to form a hemiacetal. Benzaldehyde undergoes Cannizzaro reaction because it lacks \(\alpha\)-hydrogen. \(P_2O_5\) converts carboxylic acids into acid anhydrides by dehydration.
Updated On: Jun 29, 2026
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Solution and Explanation

Concept: Aldehydes, ketones and carboxylic acids undergo a variety of important reactions due to the presence of the polar carbonyl group \((C=O)\). The carbon atom of the carbonyl group is electrophilic and therefore readily undergoes nucleophilic addition reactions. Carboxylic acids also undergo dehydration reactions in the presence of strong dehydrating agents. The given question involves three important named reactions of carbonyl compounds and carboxylic acids.

(I) Reaction of ethanal with one mole of methanol in presence of dry HCl

Step 1: Nature of reaction Alcohols add to aldehydes in the presence of dry acid catalysts. When one mole of alcohol reacts with one mole of aldehyde, the product obtained is called a

hemiacetal.

Step 2: Reaction \[ CH_3CHO + CH_3OH \xrightarrow{\text{dry HCl}} CH_3CH(OH)(OCH_3) \]

Step 3: Product formed The product contains both an \(-OH\) group and an \(-OCH_3\) group attached to the same carbon atom. Hence the product is: \[ \boxed{CH_3CH(OH)(OCH_3)} \] which is called the hemiacetal of ethanal.

(II) Benzaldehyde treated with concentrated NaOH

Step 1: Identify the reaction Benzaldehyde does not contain an \(\alpha\)-hydrogen atom. Therefore it cannot undergo aldol condensation. Instead, in concentrated sodium hydroxide solution, it undergoes the Cannizzaro reaction.

Step 2: Cannizzaro reaction In this reaction one molecule of benzaldehyde gets oxidized to benzoic acid while another molecule gets reduced to benzyl alcohol. \[ 2C_6H_5CHO + NaOH \rightarrow C_6H_5CH_2OH + C_6H_5COONa \]

Step 3: Products formed The products are: \[ \boxed{C_6H_5CH_2OH} \] (Benzyl alcohol) and \[ \boxed{C_6H_5COONa} \] (Sodium benzoate)

(III) Ethanoic acid heated with \(P_2O_5\)

Step 1: Role of \(P_2O_5\) Phosphorus pentoxide is a powerful dehydrating agent. It removes a molecule of water from two molecules of carboxylic acid.

Step 2: Formation of acid anhydride \[ 2CH_3COOH \xrightarrow{P_2O_5} (CH_3CO)_2O + H_2O \]

Step 3: Product formed The product obtained is acetic anhydride. \[ \boxed{(CH_3CO)_2O} \]

Final Answers \[ \boxed{CH_3CH(OH)(OCH_3)} \] \[ \boxed{C_6H_5CH_2OH + C_6H_5COONa} \] \[ \boxed{(CH_3CO)_2O} \]
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