The major product in the reaction is:

For the following compounds,the correct statement$(s)$ with respect to nucleophilic substitution reactions is(are):
$I$: Benzyl bromide $(C_6H_5CH_2Br)$
$II$: Cyclohexylmethyl bromide $(C_6H_{11}CH_2Br)$
$III$: tert-Butyl bromide $((CH_3)_3CBr)$
$IV$: $1-$Phenylethyl bromide $(C_6H_5CH(CH_3)Br)$
$A$. $I$ and $III$ follow $S_{N}1$ mechanism
$B$. $I$ and $II$ follow $S_{N}2$ mechanism
$C$. Compound $IV$ undergoes inversion of configuration
$D$. The order of reactivity for $I$,$III$ and $IV$ is: $IV > I > III$

For the following reactions,which of the following statements is correct?
$A. \, CH_3CH_2CH_2Br + KOH \rightarrow CH_3CH=CH_2 + KBr + H_2O$
$B. \, (CH_3)_2CHBr + KOH \rightarrow (CH_3)_2CHOH + KBr$
$C. \, C_6H_{10} + Br_2 \rightarrow C_6H_{10}Br_2$

Which one of the following is likely to give a precipitate with $AgNO_3$ solution?

Ethyl orthoformate is formed by heating which of the following compounds with sodium ethoxide?

Which of the following is likely to undergo racemization during alkaline hydrolysis?