Which one among the following undergoes dehydrohalogenation most readily?

  • A
    $(H_3C)_2CHCl$
  • B
    $(H_3C)_2CHI$
  • C
    $(H_3C)_2CHBr$
  • D
    $(H_3C)_3CI$

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In the given reaction $3-$Bromo$-2,2-$dimethylbutane $\xrightarrow{C_2H_5OH}$ (Major product) $'A'$. Product $A$ is:

Hydrolysis of an alkyl bromide $X$ $(C_5H_{11}Br)$ follows first-order kinetics. Reaction of $X$ with $Mg$ in dry ether followed by treatment with $D_2O$ gives $Y$. What is $Y$?

Which of the following factors increases the rate of a unimolecular nucleophilic substitution $(S_N1)$ reaction?

Which alkyl halide undergoes the ${S}_{N}1$ reaction most rapidly?

Arrange the following halides in decreasing order of $S_N1$ reactivity:
$(I)$ $CH_3CH_2CH_2Cl$
$(II)$ $CH_2=CHCHClCH_3$
$(III)$ $CH_3CH_2CHClCH_3$

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