Question:medium

Assertion (A): Monobromination of aniline can be conveniently done by protecting the amino group by acetylation.
Reason (R): Acetylation increases the activation effect of the amino group.

Show Hint

Acetylation lowers (not raises) the activating power of −NH₂, so the Reason is false.
Updated On: Jun 16, 2026
  • Both Assertion (A) and Reason (R) are true and Reason (R) is the correct explanation of the Assertion (A).
  • Both Assertion (A) and Reason (R) are true, but Reason (R) is not the correct explanation of the Assertion (A).
  • Assertion (A) is true, but Reason (R) is false.
  • Assertion (A) is false, but Reason (R) is true.
Show Solution

The Correct Option is C

Solution and Explanation

Step 1: Where the trap lies.
Check the assertion and reason one at a time. The catch in this question is hidden in the single word 'increases' inside the reason, so read it carefully.

Step 2: Test the assertion.
The $\mathrm{-NH_2}$ group activates aniline so powerfully that plain bromination floods the ring and gives the tribromo product. By first converting $\mathrm{-NH_2}$ into $\mathrm{-NHCOCH_3}$ through acetylation, we calm the ring down and obtain a single bromo product. So the assertion is true.

Step 3: Test the reason.
Acetylation actually reduces the activating power of the amino group, because the nitrogen lone pair is now drawn towards the C=O group and is less available to the ring. The reason claims it increases the activation, which is the opposite of the truth, so the reason is false.

Step 4: Conclusion.
A true assertion paired with a false reason fits option (C).
\[ \boxed{\text{Option (C): A true, R false}} \]
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