react anniline with NaNO2 and HCl in 273-278K to get benzene diazonium chloride.React this with CuCN and KCN to get a benzonitrile.Reduce this in presence of LiAlH4 or Ni/Pd catalyst to get benzylamine. hope u get it!
Approved
Last Activity: 13 Years ago
sanjay sanjeev patro
C6H6-NH2+CH3I---->C6H5NCH3+HI
Last Activity: 13 Years ago
Raghuvaran varan Chandragiri
The f irst project describes the synthesis of 4-arylhexahy&opy~olo[3,2-c]quinolines. The one pot ... electron donating groups on the aniline results in impure products. ...... hexahydropyrrolo[3,2-clquinoline-1-carbothioic acid benzylamide. (56)
Last Activity: 13 Years ago
Raghuvaran varan Chandragiri
Aniline is more basic due to the strong electron withdrawing effect of the carbonyl oxygen on the amide of acetanilide.
Aniline is more basic due to the strong electron withdrawing effect of the carbonyl oxygen
Aniline is much less basic than cyclohexyl amine
Last Activity: 13 Years ago
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