schiff's base formed when aniline is heated with benzaldehyde
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I think it should be - diphenylimine.
Derivatives of ammonia when allowed to react with benzaldehyde under heating conditions will lead to protonation and loss of water/ The transfer of proton will result in the formation of a Schiff's base or an imine.
Imines have a C=N bonding.
Derivatives of ammonia when allowed to react with benzaldehyde under heating conditions will lead to protonation and loss of water/ The transfer of proton will result in the formation of a Schiff's base or an imine.
Imines have a C=N bonding.
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