Which of the following carbocations is most stable :
(A)(see structure)
(B)(see structure)
(C)(see structure)
(D)(see structure)✓ Correct
Answer: (D)
Solution
The most stable carbocation is option (D) because it has extended conjugation. The positive charge can be delocalized through the conjugated system involving the double bonds and the methoxy group (–OCH₃). The methoxy group is electron-donating through resonance (+M effect), which stabilizes the adjacent positive charge. The extended conjugation over multiple double bonds provides maximum resonance stabilization compared to the other options.
JEE Main · 2022 · 29 Jun 2022 · Shift 2 · Single correct option