Question

Can someone please send me the answers to these real fast. don't post b.s. just do get points unless you wanna be reported.​

Answer 1

Answer and Explanation:

(A) IUPAC name of  the product formed will be 1-Chloro cyclohexane

$\blacksquare$ Alcohols on treating with SOCl₂ can turned into respective alkyl chlorides

$\blacksquare$ The adjoining figure shows the reaction

(B) 1-Chloro cyclohexane will undergo Sₙ2 faster

$\blacksquare$ Sₙ2 is a one step mechanism

$\blacksquare$ In Sₙ2 when the nucleophile is attacking from one side, the leaving group leaves from the opposite side

$\blacksquare$ In the given 2 compounds, 1-Methylchloride cyclohexane will undergo Sₙ2 slower due to steric hindrance from methyl group

$\blacksquare$ In 1-Chloro cyclohexane there is not much steric hindrance