An alkyl halide may be converted into an alcohol by

  • A
    Elimination
  • B
    Addition
  • C
    Substitution
  • D
    Dehydrohalogenation

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Similar Questions

In the following reactions,
$(i) CH_3-CH(CH_3)-CH(OH)-CH_3 \xrightarrow{H^{+}/\text{heat}} A \text{ [Major product]} + B \text{ [Minor product]}$
$(ii) A$ $\xrightarrow[\text{in absence of peroxide}]{HBr, \text{dark}} C \text{ [Major product]} + D \text{ [Minor product]}$
the major products $(A)$ and $(C)$ are respectively:

The major product of the reaction between $CH_{3}CH_{2}ONa$ and $(CH_{3})_{3}CCl$ in ethanol is

In the following pairs of halogen compounds,which compound undergoes faster $S_N 1$ reaction?

Arrange the following in order of ease of dehydrohalogenation:
$(i)$ Bromocyclohexane
(ii) $3-$Bromocyclohexene
(iii) $3-$Bromocyclohexa$-1,4-$diene
(iv) Bromobenzene

Difficult
View Solution

Given below are two statements: one is labelled as Assertion $(A)$ and the other is labelled as Reason $(R)$.
Assertion $(A):$ $R-I$ undergoes $S_N2$ reaction faster than $R-Cl$.
Reason $(R):$ Iodine is a better leaving group because of its large size.
In the light of the above statements,choose the correct answer from the options given below:

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