Carbocation as an intermediate is likely to be formed in the reaction :

Question

Carbocation as an intermediate is likely to be formed in the reaction : (A) Acetone +HCN xrightarrow-OH acetonecyanohydrin (B) Hexane xrightarrow textAnhy . AlCl3 /HCl 2-methyl pentane (C) Propene + +Cl2 xrightarrowhv 2-chloropropane (D) Ethylbromide + Aq KOH xrightarrowΔ ethyl alcohol

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<img class="img-fluid question-image" alt="image" src="https://cdn.tardigrade.in/img/question/chemistry/4fa388025983ac59a1d21e4d0e854231-.png" /> This reaction is a result of molecular rearrangement involving 1,2 -hydride or methyl shift. This rearrangement occurs via carbocations, which are generated by the acidic catalyst.

Q. Carbocation as an intermediate is likely to be formed in the reaction :

Acetone $+ H CN - O H$ acetonecyanohydrin

Hexane $Anhy . A lC l_{3} / H Cl$ 2-methyl pentane

Propene + $+ C l_{2} h v$ 2-chloropropane

Ethylbromide $+ A q K O H Δ$ ethyl alcohol

This reaction is a result of molecular rearrangement involving 1,2 -hydride or methyl shift. This rearrangement occurs via carbocations, which are generated by the acidic catalyst.

Q. Carbocation as an intermediate is likely to be formed in the reaction :

Acetone +HCN−OH​ acetonecyanohydrin

Hexane Anhy.AlCl3​/HCl​ 2-methyl pentane

Propene + +Cl2​hv​ 2-chloropropane

Ethylbromide +AqKOHΔ​ ethyl alcohol

This reaction is a result of molecular rearrangement involving 1,2 -hydride or methyl shift. This rearrangement occurs via carbocations, which are generated by the acidic catalyst.

Acetone $+ H CN - O H$ acetonecyanohydrin

Hexane $Anhy . A lC l_{3} / H Cl$ 2-methyl pentane

Propene + $+ C l_{2} h v$ 2-chloropropane

Ethylbromide $+ A q K O H Δ$ ethyl alcohol