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Statement -1: Acetophenone gives aldol c...

Statement -1: Acetophenone gives aldol condensation.
Statement-2: Benzaldehyde is more reactive than acetaldehyde towards nucleophilic addition.
Statement-3: Benzophenone has `alpha`-Hydrogens

A

TTT

B

FFF

C

TFF

D

TFT

Text Solution

Verified by Experts

The correct Answer is:
C
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Why a benzaldehyde less reactive than acetaldehyde towards nucleophilic addition reactions?

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Knowledge Check

  • Statement-1: Formaldehyde is more reactive than benzaldehyde for nucleophilic addition reaction. Statement-2: Formaldehyde is more stable than benzaldehyde.

    A
    Statement-1 is True, Statement-2 is True, Statement-2 is a correct explanation for statement-1
    B
    statement-1 is true, statement-2 is true, statement-2 is NOT a correct explanation for statement-1
    C
    statement-1 is true, statement-2 is false
    D
    statement-1 is false, statement-2 is true

  • Statement-1. Acetylene is more reactive than ethylene towards electrophilic addition reactions Statement-2. Acetylene contains two pi -bonds

    A
    Statement-1 is True, Statement-2 is True , Statement-2 is a correct explanation for Statement-1
    B
    Statement-1 is True, Statement-2 is True , Statement-2 is not a correct explanation for Statement-1
    C
    Statement- 1 is True, Statement-2 is False
    D
    Statement-1 is False, Statement -2 is True

  • Statement-1: Chloroacetaldehyde is more reactive than acetaldehyde for nucleophilic addition reaction. Statement-2: I group in carbonyl compound makes carbonyl carbon more electron deficient.

    A
    Statement-1 is True, Statement-2 is True, Statement-2 is a correct explanation for statement-2
    B
    statement-1 is true, statement-2 is true, statement-2 is NOT a correct explanation for statement-2
    C
    statement-1 is true, statement-2 is false
    D
    statement-1 is false, statement-2 is true

    • Similar Questions

    Explore conceptually related problems

    Give reason : Aldehydes are more reactive than ketones towards nucleophilic reagents.

    Assertion : Benzaldehyde is less reactive than propanal towards nucleophilic addition reactions. Reason : Benzaldehyde is less sterically hindred.

    STATEMENT -I : Benzaldehyde is more reactive then acetaldehyde towards nucleophilic addition STATEMENT -2 : In benzaldehyde C=O group is resonance stabilised by phenyl ring.

    Statement -I: Nitromethane can give aldol condensation. Statement - II: alpha - hydrogen of nitromethane is acidic.

    Assertion (A): Benzaldehyde is less reactive than ethanal towards nucleophilic addition reactions. Reason (R): Ethanal is more sterically hindered.

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