In the Gabriel phthalimide synthesis,phthalimide is treated first with

  • A
    $C_2H_5I / KOH$
  • B
    Ethanolic $Na$
  • C
    Ethanol and $H_2SO_4$
  • D
    Ether and $LiAlH_4$

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Similar Questions

Acetamide is treated separately with the following reagents. Which would give methyl amine?

In which case is an alkylamine not formed?

Hofmann degradation is given by:

Why cannot aromatic primary amines be prepared by Gabriel phthalimide synthesis?

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Secondary amines can be prepared by $:-$

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