Tertiary alkyl halides are practically inert to substitution by $S_N2$ mechanism because of:

  • A
    Insolubility
  • B
    Instability
  • C
    Inductive effect
  • D
    Steric hindrance

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The product $B$ formed in the following reaction sequence is:

Reaction of trans-$2-$phenyl$-1-$bromocyclopentane with alcoholic $KOH$ produces:

An alkyl bromide $(A)$ forms a Grignard reagent which on treatment with water yields $n$-hexane. When $(A)$ is treated with sodium in dry ether,$4,5$-diethyloctane is formed. The structure of $(A)$ is:

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The correct order of the rate of dehydrohalogenation of the following halides in the presence of alcoholic $KOH$ is:

The product $X$ is
[Image: $1-$chloro$-1-$($2$-chloroethyl)cyclopentane] $\xrightarrow{LiBr/DMSO, S_N2 \text{ conditions}}$ Major product $(X)$

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