In the following question two Statement-I (Assertion) and Statement-2 (Reason) are provided. each question has 4 choices (a), (b), (c) and (d) for its answer, out of which Only One is correct. Mark your responses from the following options:
Statement-1: Aniline becomes more reactive towards electrophilic aromatic substitution in presence of strongly acidic solution.
Statement-2: The amino group is completely protonated in strongly acidic medium. Thus the lone pair of electrons on the nitrogen is no longer available for resonance.

Both Statement-1 and Statement-2 are true and Statement-2 is the correct explanation of Statement-1.

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Both Statement-1 and Statement-2 are true and Statement-2 is not the correct explanation of Statement-1.

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Statement-1 is true but Statement-2 is false.

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Statement-1 is false but Statement-2 is true.

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Solution

The correct option is D
Statement-1 is false but Statement-2 is true.

Assertionis false, explanation is although true but it is not correct explanation of assertion.

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In the following question two Statement-I (Assertion) and Statement-2 (Reason) are provided. each question has 4 choices (a), (b), (c) and (d) for its answer, out of which Only One is correct. Mark your responses from the following options:
Statement-1: Aniline becomes more reactive towards electrophilic aromatic substitution in presence of strongly acidic solution.
Statement-2: The amino group is completely protonated in strongly acidic medium. Thus the lone pair of electrons on the nitrogen is no longer available for resonance.

Q. Assertion :In strongly acidic solutions, aniline becomes more reactive towards electrophilic reagents. Reason: The amino group being completely protonated in strongly acidic solution, the lone pair of electrons on nitrogen is no longer available for resonance.

Q. Assertion :In strongly acidic solutions, aniline becomes more reactive towards electrophilic reagents Reason: The amino group being completely protonated in strongly acidic solution, the lone pair electrons on the nitrogen is no longer avaiable for resonance.

In the following question two Statement-I (Assertion) and Statement-2 (Reason) are provided. each question has 4 choices (a), (b), (c) and (d) for its answer, out of which Only One is correct. Mark your responses from the following options:
Statement-1: 2-Pentyne on hydrogenation in presence of Lindlar catalyst gives cis-1-pentene.
Statement-2: Addition of hydrogen is a stereospecific reaction.

In the following questions two Statement-1 (Assertion) and Statement-2 (Reason) are provided. Each questions has 4 choices (a), (b), (c) and (d) for its answer, out of which ONLY ONE is correct. Mark your responses from the following options:
Statement- 1: 1-Butene on reaction with HBr in the presence of a peroxide produces 1-bromobutane.
Statement- 2: It involves the formation of a primary radical.

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The correct option is D Statement-1 is false but Statement-2 is true. Assertionis false, explanation is although true but it is not correct explanation of assertion.

The correct option is D
Statement-1 is false but Statement-2 is true.

Assertionis false, explanation is although true but it is not correct explanation of assertion.