Identify Z in the reaction sequence: CH_3CH_2 | vedclass

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(B) $1$. $CH_3CH_2CH_2Br$ reacts with aqueous $NaOH$ (nucleophilic substitution) to form propan-$1$-ol $(X)$: $CH_3CH_2CH_2Br + NaOH(aq) \rightarrow C

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$CH_3CHOHCH_2Cl$

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(B) $1$. $CH_3CH_2CH_2Br$ reacts with aqueous $NaOH$ (nucleophilic substitution) to form propan-$1$-ol $(X)$: $CH_3CH_2CH_2Br + NaOH(aq) \rightarrow CH_3CH_2CH_2OH + NaBr$.$2$. Propan-$1$-ol $(X)$ undergoes dehydration with $Al_2O_3$ at high temperature to form propene $(Y)$: $CH_3CH_2CH_2OH \xrightarrow{Al_2O_3, \Delta} CH_3CH=CH_2 + H_2O$.$3$. Propene $(Y)$ reacts with $Cl_2/H_2O$ (hypochlorous acid,$HOCl$) to form chlorohydrin $(Z)$: $CH_3CH=CH_2 + Cl_2 + H_2O \rightarrow CH_3CH(OH)CH_2Cl + HCl$. The hydroxyl group attaches to the more substituted carbon (Markovnikov addition).

Identify $Z$ in the reaction sequence: $CH_3CH_2CH_2Br$ $\xrightarrow{Aq. NaOH} X$ $\xrightarrow{Al_2O_3, \Delta} Y$ $\xrightarrow{Cl_2/H_2O} Z$

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