Statement I : Benzene is nitrated to give nitrobenzene, which on further treatment with CH3COCl/AlCl3 will give
(A)Statement I is correct but Statement II is incorrect.
(B)Both Statement I and Statement II are correct.
(C)Statement I is incorrect but Statement II is correct.✓ Correct
(D)Both Statement I and Statement II is are incorrect.
Answer: (C)
Solution
Nitration of benzene gives nitrobenzene, but the nitro group is strongly electron-withdrawing and deactivates the ring so heavily that nitrobenzene does not undergo Friedel-Crafts acylation; treatment with acetyl chloride and aluminium chloride gives essentially no ketone, so the claim in Statement I that it yields m-nitroacetophenone is incorrect. The nitro group is a meta-directing, deactivating substituent, which is the correct content of Statement II. Hence Statement I is incorrect but Statement II is correct.
JEE Main · 2026 · 22 Jan 2026 · Shift 1 · Single correct option