Which of the following reactions can be used to convert an alkyl halide into an alcohol?

  • A
    Addition
  • B
    Substitution
  • C
    Dehydrohalogenation
  • D
    Molecular rearrangement

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Similar Questions

Which of the following is least reactive towards $S_N2$ reaction?

Which of the following will give $S_N2$ reaction at the fastest rate?

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Arrange the leaving group ability of the following groups in decreasing order:
$(I)$ $CH_3-C_6H_4-SO_3^-$,$(II)$ $C_6H_5-SO_3^-$,$(III)$ $N_3^-$,$(IV)$ $Br^-$

Which of the following is most reactive toward $S_N2$ reaction?

The rate of $\beta$-dehydrohalogenation in the following halides under treatment with a strong base follows the order:

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