Diborane reacts with terminal alkenes to form trialkylboranes. These react with alkaline hydrogen peroxide to form:

  • A
    Primary alcohol
  • B
    Secondary alcohol
  • C
    Tertiary alcohol
  • D
    Isobutyl alcohol

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An alkene $A$ on reaction with $O_{3}$ and $Zn-H_{2}O$ gives propanone and ethanal in equimolar ratio. Addition of $HCl$ to alkene $A$ gives $B$ as the major product. The structure of product $B$ is:

Arrange the following compounds in the order of their reactivity towards electrophilic addition reaction with $HBr$.

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What is obtained by the dehydrohalogenation of allyl chloride?

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The incorrect method for the synthesis of alkenes is:

What is the major product expected from the following reaction?
Where $D$ is an isotope of hydrogen.

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