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Draw the zwitter ion structure for sulphanilic acid.
How can the activating effect of –NH₂ group in aniline be controlled ?
Convert Bromoethane to Propanamine.
Give reasons :
Give reasons: (i) Aniline on nitration gives good amount of m-nitroaniline, though – NH₂ group is o/p directing in electrophilic substitution reactions. (ii) (CH₃)₂ NH is more basic than (CH₃)₃N in an aqueous solution. (iii) Ammonolysis of alkyl halides is not a good method to prepare pure primary amines.
Write the reaction involved in the following: (i) Carbyl amine test (ii) Gabriel phthalimide synthesis
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