Complete reduction of $benzene-diazonium$ chloride with $Zn/HCl$ gives:

  • A
    Aniline
  • B
    Phenylhydrazine
  • C
    Azobenzene
  • D
    Hydrazobenzene

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Consider the following:
Statement-$I$: In the nitration of aniline,a significant amount of $m$-nitroaniline is formed.
Statement-$II$: In the presence of a strongly acidic medium,aniline is protonated to form the anilinium ion,which is meta-directing.

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What is obtained by the reduction of nitrobenzene with zinc and alkali?

Which of the following reagents reacts with acetamide to produce methylamine?

Aniline under acidic medium,when chlorinated,produces :

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