Elimination of bromine from $2-$bromobutane results in the formation of

  • A
    Equimolar mixture of $1-$butene and $2-$butene
  • B
    Predominantly $2-$butene
  • C
    Predominantly $1-$butene
  • D
    Predominantly $2-$butyne

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Similar Questions

For the given reaction $R-C(R_1)(R_2)-X \xrightarrow{HOH} R-C(R_1)(R_2)-OH$,which substrate will give maximum racemisation?

The product $(C)$ in the following reaction sequence is:

In the given reaction:
$CH_3-CH_2-\ddot{S}-CH_2^*-CH_2-Br \xrightarrow{HOH} [X]$
$[X]$ will be:

Iodoform on heating with $KOH$ gives

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The principal organic product of the reaction will be:

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