Question:

In which case the \( \text{NO}_2 \) will attack at the meta position? 

Show Hint

In nitration reactions, \( \text{NO}_2 \) attacks the meta position in the presence of electron-withdrawing groups.
Updated On: Mar 25, 2026
  • I, II, III
  • II, IV
  • I and III only
  • II only
Hide Solution
collegedunia
Verified By Collegedunia

The Correct Option is A

Solution and Explanation


Step 1: Nitration of aromatic compounds.

In electrophilic aromatic substitution reactions, \( \text{NO}_2 \) typically attacks the meta position in compounds that have electron-withdrawing groups attached at the ortho and para positions. Based on the structures, \( \text{NO}_2 \) attacks at the meta position in compounds I, II, and III.
Thus, the correct answer is (1).
Was this answer helpful?
0
0