$A$ student performed an analysis of an aliphatic organic compound '$X$' which, upon analysis, gave $C=61.01\%$, $H=15.25\%$, $N=23.74\%$. This compound, on treatment with $HNO_2/H_2O$, produced another compound '$Y$' which did not contain any nitrogen atom. However, the compound '$Y$' upon controlled oxidation produced another compound '$Z$' that responded to the iodoform test. The structure of '$X$' is:

  • A
    $CH_3CH_2CH_2NH_2$
  • B
    $Ph-CH(CH_3)-NH_2$
  • C
    $(CH_3)_2CH-NH_2$
  • D
    $CH_3-CH_2-CH(NH_2)-CH_3$

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