$R - X + NaOH \xrightarrow{} ROH + NaX$
The above reaction is classified as:

  • A
    Nucleophilic substitution
  • B
    Electrophilic substitution
  • C
    Reduction
  • D
    Oxidation

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The hydrolysis of $2$-bromo-$3$-methylbutane by the $S_N1$ mechanism primarily yields:

Consider the following reactions:
$(a) \; (CH_3)_3CCH(OH)CH_3 \xrightarrow{conc. H_2SO_4} $
$(b) \; (CH_3)_2CHCH(Br)CH_3 \xrightarrow{alc. KOH} $
$(c) \; (CH_3)_2CHCH(Br)CH_3 \xrightarrow{(CH_3)_3CO^{-}K^{+}} $
$(d) \; (CH_3)_2C(OH)CH_2CHO \xrightarrow{\Delta} $
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Tertiary alkyl halides are practically inert to substitution by the $S_N2$ mechanism due to:

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