Hydration of 3-phenylbut-1-ene in dil. H_2SO_ | vedclass

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(C) The hydration of $3$-phenylbut$-1$-ene in dilute $H_2SO_4$ proceeds via the formation of a carbocation intermediate.$1$. Protonation of the double

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$2$-Phenylbutan-$2$-ol

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(C) The hydration of $3$-phenylbut$-1$-ene in dilute $H_2SO_4$ proceeds via the formation of a carbocation intermediate.$1$. Protonation of the double bond occurs to form a $2^{\circ}$ carbocation: $CH_3-CH(C_6H_5)-CH^+-CH_3$.$2$. This $2^{\circ}$ carbocation undergoes a $1,2$-hydride shift to form a more stable $3^{\circ}$ benzylic carbocation: $CH_3-CH_2-C^+(C_6H_5)-CH_3$.$3$. Finally,the nucleophilic attack of $H_2O$ on the $3^{\circ}$ carbocation followed by deprotonation yields $2$-phenylbutan-$2$-ol as the major product.

Hydration of $3$-phenylbut$-1$-ene in dil. $H_2SO_4$ will give mainly

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