Fundamentholfundamenthol
JEE Main2026Apr 2, Shift 2Chemistry
Q.

The compound (X) on

(i) on heating in the presence of anhydrous AlCl and HCl gas gives -dimethyl pentane

(ii) aromatization gives toluene and

(iii) cyclisation gives methyl cyclohexane

The correct name of compound (X) is :

  1. A

    Hept-2-ene

  2. B

    Hept-1,3,5-triene

  3. C

    Heptane

  4. D

    Hept-2,4,6-triene

Solution

All three reactions are characteristic of -heptane (a straight-chain C alkane):

(i) Isomerisation with anhydrous AlCl/HCl converts -heptane to its branched isomer -dimethylpentane.

(ii) Aromatisation (dehydrocyclisation) over CrO/AlO at high temperature converts -heptane to toluene (loss of H).

(iii) Catalytic cyclisation produces methylcyclohexane (loss of H).

The triene options would not give these specific products under these conditions, and hept--ene would not produce -dimethylpentane on isomerisation.

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