In the following reaction sequence,$C_2H_5NH_2$ $\xrightarrow{HNO_2} A$ $\xrightarrow{PCl_5} B$ $\xrightarrow{NH_3} C$,the compound '$C$' is

  • A
    $CH_3NH_2$
  • B
    $C_2H_5NH_2$
  • C
    $CH_3CH=NH$
  • D
    $(CH_3)_2NH$

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$A$ primary amine,$RNH_2$ can be reacted with $CH_3-X$ to get a secondary amine,$RNHCH_3$,but the disadvantage is that $3^o$ amine and quaternary ammonium salts are also obtained as side products. Can you suggest a method where $RNH_2$ forms only $2^o$ amine?

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