(D) The reaction involves $tert-$butyl chloride and potassium $tert-$butoxide $(t-BuOK)$.$t-BuO^-$ is a bulky base.Due to steric hindrance,the bulky b

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(D) The reaction involves $tert-$butyl chloride and potassium $tert-$butoxide $(t-BuOK)$.$t-BuO^-$ is a bulky base.Due to steric hindrance,the bulky base cannot attack the electrophilic carbon for substitution $(S_N2)$.Instead,it abstracts a $\beta-$hydrogen from the $tert-$butyl chloride,leading to an elimination reaction ($E2$ mechanism).The product formed is $2-$methylprop$-1-$ene.

Class 12 Chemistry Haloalkanes and Haloarenes Properties of Haloalkanes

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The major product in the reaction is:

JEE MAIN 2022 All JEE MAIN

A
$t-$Butyl ethyl ether
B
$2,2-$Dimethyl butane
C
$2-$Methyl pent$-1-$ene
D
$2-$Methyl prop$-1-$ene

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Class 12

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Chapter

Haloalkanes and Haloarenes

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Properties of Haloalkanes

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Consider the following bromides.
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MediumAIIMS 2016

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The organic chloro compound,which shows complete stereochemical inversion during an $S_{N}2$ reaction,is

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$CH_3-CH_2-C(Br)(CH_2CH_3)-CH_2(CH_2CH_2CH_3) \xrightarrow{alc. KOH} (A)$ (major)
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Product $(A)$ is

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$A$ solution of $(-)-1-$chloro$-1-$phenylethane in toluene racemises slowly in the presence of a small amount of $SbCl_5$,due to the formation of:

DifficultJEE MAIN 2013

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An isomer of $C_3H_6Cl_2$ on boiling with aqueous $KOH$ gives acetone. Hence,the isomer is

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The major product in the reaction is:

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