Advertisements
Advertisements
प्रश्न
Account for the following:
Gabriel phthalimide synthesis is not preferred for preparing aromatic primary amines.
Advertisements
उत्तर
Gabriel phthalimide synthesis not prefered for preparing aromatic primary amines because amine formation involves nucleophilic substituion 2 ( ) SN of alkyl halides by the anion formed by the phthalimide. But aryl halides do not undergo nucleophilic substitution with the anion formed by the phthalimide. As nucleophilic substitution reactions are very difficult in aryl halides.
APPEARS IN
संबंधित प्रश्न
Write the chemical equation involved in the following reaction:
Hoffmann-bromamide degradation reaction
Write reactions for the preparation of ethanamine using Gabriel phthalimide synthesis.
Identify the product 'A' in the following reaction.
\[\ce{Aniline ->[(CH3CO)2O][Pyridine] A}\]
Identify the product obtained when benzyl chloride undergoes ammonolysis in presence of excess ammonia followed by the reaction with two moles of methyl iodide.
\[\ce{CH3-CN ->[Na/C2H5OH]}\]
The product formed is ____________.
Among the following amines, the strongest Brönsted base is:
Suggest a route by which the following conversion can be accomplished.

Which of the following compound is expected to be most basic?
Identify the compo ds A and B in the following reactions:
\[\ce{A ->[Nitrating mixture] B ->[(i) Sn/cone. HCI][(ii) NaOH] Aniline}\]
Write a short note on the following:
Ammonolysis
