NEET 2026 Chemistry Question 46 Solution
Question
For the following reaction sequence, choose the correct option: Benzene → i. CH₃COCl, AlCl₃ ii. NaOCl → P + Q
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For the following reaction sequence, choose the correct option: Benzene → i. CH₃COCl, AlCl₃ ii. NaOCl → P + Q
Spot the tandem: Benzene + Acetyl Chloride = Acetophenone (a methyl ketone). NaOCl is the textbook Haloform reagent!
Benzene reacts with acetyl chloride in the presence of anhydrous aluminium chloride (Lewis acid catalyst). An acylium ion (CH₃-C⁺=O) is generated, which attacks the benzene ring to yield acetophenone.
Acetophenone contains the characteristic -COCH₃ group attached to carbon. Sodium hypochlorite (NaOCl), an aqueous mixture of chlorine and sodium hydroxide, oxidizes and halogenates the methyl ketone. Tri-alpha chlorination occurs followed by hydroxide attack and cleavage of the C-C bond to yield Sodium Benzoate (P) and Chloroform (Q).
Acidification of sodium benzoate (P) yields Benzoic Acid (C₆H₅COOH). When chloroform (Q) is exposed to atmospheric oxygen in the presence of sunlight, it undergoes slow photochemical oxidation to form carbonyl chloride (Phosgene, COCl₂), an extremely poisonous gas.
Diagnose every choice: Know exactly why the right option works and why distractors fail.
Completely false. P is sodium benzoate (C₇H₅O₂Na) and Q is chloroform (CHCl₃); their molecular weights and atom compositions are entirely different.
Incorrect. Neither an alcohol nor an ether is generated in haloform cleavage of a methyl ketone.
Scientifically rigorous. P = Sodium benzoate (acidifies to Benzoic Acid) and Q = Chloroform (oxidizes to poisonous Phosgene gas COCl₂).
Incorrect. Chloroform (CHCl₃) with base undergoes alpha-elimination to generate dichlorocarbene (:CCl₂), or hydrolyzes to sodium formate (HCOONa), not an alkene.
Students frequently remember the haloform mechanism but forget the industrial toxicology of chloroform (photochemical oxidation to phosgene COCl₂).
"Methyl ketones undergo hypohalite cleavage to yield carboxylate salts and trihalomethanes. Chloroform photochemically oxidizes to phosgene."
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