Which of the following reactions occurs by the removal of a $-CO-$ group from an amide?

  • A
    $\text{Gabriel phthalimide synthesis}$
  • B
    $\text{Ammonolysis of halides}$
  • C
    $\text{Mendius reduction}$
  • D
    $\text{Hofmann degradation}$

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Indicate which nitrogen compound amongst the following would undergo Hofmann's reaction (i.e.,reaction with $Br_2$ and strong $KOH$) to furnish the primary amine $(R-NH_2)$.

Which of the following compounds can be prepared in good yield by Gabriel phthalimide synthesis?

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Gabriel phthalimide synthesis is used for the preparation of which of the following?

Which of the following do not give aliphatic primary amine as a product?

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