$A$ hydrocarbon with molecular formula $C_4H_6$ undergoes the following reactions:
$A$. Decolourises molecular bromine.
$B$. Reacts with $HBr$.
$C$. Addition of ozone and then cleavage of the ozonide by $Zn / H_2O$ gives the product $C_4H_6O_2$.
Then,the structure of the hydrocarbon is:

  • A
    Cyclobutene
  • B
    None of these
  • C
    $CH_3CH_2C \equiv CH$
  • D
    Methylenecyclopropane

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