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प्रश्न
Account for the following:
Gabriel phthalimide synthesis is not preferred for preparing aromatic primary amines.
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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.
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संबंधित प्रश्न
Accomplish the following conversion:
Benzamide to toluene
Answer the following
Explain Gabriel phthalimide synthesis.
____________ can be prepared exclusively by Gabriel phthalimide synthesis.
Identify the product obtained when benzamide is treated with bromine and aqueous sodium hydroxide?
Quaternary ammonium salt is formed:
Amongst the following, the strongest base in aqueous medium is ______.
The reagents that can be used to convert benzenediazonium chloride to benzene are:
(i) \[\ce{SnCl2/HCl}\]
(ii) \[\ce{CH3CH2OH}\]
(iii) \[\ce{H3PO2}\]
(iv) \[\ce{LiAlH4}\]
Account for the following:
Aniline cannot be prepared by the ammonolysis of chlorobenzene under normal conditions.
C6H5CONHCH3 can be converted into C6H5CH2NHCH3 by:-
Write a short note on the following:
Ammonolysis
