Assertion: $2-$Bromobutane on reaction with sodium ethoxide in ethanol gives $1-$butene as a major product.
Reason: $1-$Butene is more stable than $2-$butene. According to Saytzeff's rule,$2-$butene should be the product which is more branched or substituted compound and hence,more stable than $1-$butene.

  • A
    If both Assertion and Reason are correct and the Reason is a correct explanation of the Assertion.
  • B
    If both Assertion and Reason are correct but Reason is not a correct explanation of the Assertion.
  • C
    If the Assertion is correct but Reason is incorrect.
  • D
    If both the Assertion and Reason are incorrect.

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Similar Questions

The product $X$ is
[Image: $1-$chloro$-1-$($2$-chloroethyl)cyclopentane] $\xrightarrow{LiBr/DMSO, S_N2 \text{ conditions}}$ Major product $(X)$

In the given pair of compounds,in which pair is the second compound more reactive than the first toward $S_N2$ reaction?

Difficult
View Solution

Explain elimination reactions of alkyl halides.
or
Explain dehydrohalogenation ($\beta$-elimination) of alkyl halides.

For the reaction:
$RCH_2Br + I^{-} \stackrel{\text{Acetone}}{\longrightarrow} RCH_2I + Br^{-}$
The correct statement is:

Which of the following alkyl halides undergoes a substitution reaction according to the $S_{N}1$ mechanism?

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