Question

Solve the reaction.

Answer 1

@Munzir,

I made a mistake. Your answer option B is correct

Explanation 

Protonation of oxygen atom opens the epoxide ring forming a secondary carbo cation as well as a -OH group.

A 5 membered ring formation then occurs due delocalization of electron from =CH₂ forming a tertiary carbocation. This carbocation is then attacked by water molecule and finally a -OH group is formed there releasing a proton.

Comments

Please can u write the chemical reaction.

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Using phone now. I can try it later from desktop.

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Okk.Thank You

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Thank you for the answer.