In which pairs, the first ion is more stable than the second?

Question

Canvas Classes · Accepted Answer

Step 1: Stability Analysis
- (A): . Para-methoxy group provides +M effect, stabilizing the carbocation.
- (B): . Para-nitro group provides -M/-I effect, destabilizing the carbocation.

Step 2: Evaluating the Pairs
Pair (A)  Pair (B) based on resonance stabilization vs. destabilization.

Step 3: Conclusion
Methoxy-substituted benzyl cation is more stable than nitro-substituted.

More questions from GOC