Question:

Assertion (A): p-Nitroaniline is a weaker base than p-toluidine. Reason (R): The electron-withdrawing effect of \(-NO_2\) group in p-nitroaniline makes it a weaker base.

Show Hint

Electron-withdrawing groups decrease basicity, while electron-donating groups increase basicity in aromatic amines.
Updated On: Feb 25, 2025
  • 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.
Hide Solution
collegedunia
Verified By Collegedunia

The Correct Option is A

Solution and Explanation

- p-Nitroaniline is weaker than p-toluidine because the \(-NO_2\) group is electron-withdrawing (-M and -I effect), decreasing the electron density on the nitrogen of the amine, reducing its basicity. - In contrast, the \(-CH_3\) group in p-toluidine is electron-donating (+I effect), increasing electron density on nitrogen and enhancing basicity. - Since both the assertion and reason are correct, and Reason (R) explains Assertion (A), option (A) is correct.
Was this answer helpful?
0
0

Top Questions on Amines

View More Questions

Questions Asked in CBSE CLASS XII exam

View More Questions