Ozonolysis of the given compound yields:

  • A
    Cyclopentanone + Formaldehyde
  • B
    Cyclopentanecarbaldehyde
  • C
    Acetylcyclopentane
  • D
    None of these

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Which of the following is the most stable alkene?

Which of the following alkyl-substituted alkenes is the most stable?

How many products will be formed in the reaction shown below?
$CH_3-CH_2-C(CH_3)=C(CH_3)-CH_2-CH_3 + HBr \xrightarrow{R_2O_2} \text{Products}$

The addition of $HI$ to the double bond of propene yields isopropyl iodide and not $n$-propyl iodide because the addition proceeds through the formation of:

The major product of the following reaction sequence is:

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