Correct statements regarding alkyl halides ( R−X ) among the following are : (A) Alcohol being less polar solvent as compared to water, alcoholic KOH favours elimination reaction with R−X. (B) Order of reactivity towards SN1 mechanism is C6H5−CH2−Cl>C6H5−CHCl−C6H5. (C) Non substituted aryl halides exhibit properties similar to alkyl halides. (D) Vinyl chloride is an example of haloalkene and allyl chloride is an example of haloalkyne. (E) R−Cl can be prepared by reacting R−OH with SOCl2 but Ar−Cl cannot be prepared by reacting Ar−OH with SOCl2.
Choose the correct answer from the options given below :
(A)A, B and C Only
(B)B and D Only
(C)A and E Only✓ Correct
(D)D and E Only
Answer: (C)
Solution
Alcoholic KOH, in the less polar alcohol medium, favours loss of HX by elimination over substitution, so statement A is correct. For the SN1 pathway the rate tracks carbocation stability, and the diphenylmethyl cation from CX6HX5−CHCl−CX6HX5 is more stable than the benzyl cation from CX6HX5−CHX2−Cl, so the order in statement B is reversed and it fails. Aryl halides are far less reactive than alkyl halides because the C−X bond gains partial double-bond character by resonance, so statement C fails. Allyl chloride is a haloalkene, not a haloalkyne, so statement D fails. Alcohols are converted to chlorides by SOClX2 whereas phenols are not, so statement E is correct. The correct statements are A and E.
JEE Main · 2026 · 02 Apr 2026 · Shift 2 · Single correct option