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JEE Main2026Apr 2, Shift 2Chemistry
Q.

Correct statements regarding alkyl halides (RX) among the following are :

(A) Alcohol being less polar solvent as compared to water, alcoholic KOH favours elimination reaction with RX.

(B) Order of reactivity towards S1 mechanism is CH-CH-Cl CH-CHCl-CH.

(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) RCl can be prepared by reacting ROH with SOCl but ArCl cannot be prepared by reacting ArOH with SOCl.

Choose the correct answer from the options given below :

  1. A

    A, B and C Only

  2. B

    B and D Only

  3. C

    A and E Only

  4. D

    D and E Only

Solution

(A) True. Alcoholic KOH (less polar than aqueous KOH) favours elimination () over substitution.

(B) False. S1 reactivity tracks carbocation stability; the diphenylmethyl cation (PhCH) is more stable than benzyl cation (PhCH) due to additional resonance, so CHCHCl-CH is more reactive than CHCHCl in S1.

(C) False. Aryl halides are far less reactive than alkyl halides toward nucleophilic substitution because of CX bond strengthening (partial double-bond character) and ring electron density.

(D) False. Allyl chloride (CH=CHCHCl) is a haloalkene, not a haloalkyne.

(E) True. SOCl converts aliphatic alcohols smoothly to alkyl chlorides, but phenols do not react this way to give aryl chlorides (the CO bond in ArOH has partial double-bond character).

Correct statements: A and E.

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