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 :
- A
Hept-2-ene
- B
Hept-1,3,5-triene
- C
Heptane
- D
Hept-2,4,6-triene

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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