The major product in the reaction is:

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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 b

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$2-$Methyl prop$-1-$ene

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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.

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