Arrange the following in increasing order of their basic strength: (i) C2H5NH2 , C6H5NH2 , NH3 , C6H5CH2NH2 and (C2H5 ) 2NH (ii) C2H5NH2 , (C2H5 ) 2NH, (C2H5 ) 3N, C6H5NH2 (iii) CH3NH2 , (CH3 ) 2NH, (CH3 ) 3N, C6H5NH2 , C6H5CH2NH2 .

(i) Considering the inductive effect of alkyl groups, NH₃, C₂H₅NH_2, and (C₂H₅)₂NH can be arranged in the increasing order of their basic strengths as:

Again, C₆H₅NH₂ has proton acceptability less than NH₃. Thus, we have:

Due to the −I effect of C₆H₅ group, the electron density on the N-atom in C₆H₅CH₂NH₂ is lower than that on the N-atom in C₂H₅NH_2, but more than that in NH₃. Therefore, the given compounds can be arranged in the order of their basic strengths as:

(ii) Considering the inductive effect and the steric hindrance of the alkyl groups, C₂H₅NH₂, (C₂ H₅)₂NH_2, and their basic strengths as follows:

Again, due to the −R effect of C₆H₅ group, the electron density on the N atom in C₆H₅ NH₂ is lower than that on the N atom in C₂H₅NH₂. Therefore, the basicity of C₆H₅NH₂ is lower than that of C₂H₅NH₂. Hence, the given compounds can be arranged in the increasing order of their basic strengths as follows:

(iii) Considering the inductive effect and the steric hindrance of alkyl groups, CH₃NH₂, (CH₃)₂NH, and (CH₃)₃N can be arranged in the increasing order of their basic strengths as:

In C₆H₅NH₂, N is directly attached to the benzene ring. Thus, the lone pair of electrons on the N−atom is delocalized over the benzene ring. In C₆H₅CH₂NH₂, N is not directly attached to the benzene ring. Thus, its lone pair is not delocalized over the benzene ring. Therefore, the electrons on the N atom are more easily available for protonation in C₆H₅CH₂NH₂ than in C₆H₅NH₂ i.e., C₆H₅CH_2­NH₂ is more basic than C₆H₅NH₂.

Again, due to the −I effect of C₆H₅ group, the electron density on the N−atom in C₆H₅CH₂NH₂ is lower than that on the N−atom in (CH₃)₃N. Therefore, (CH₃)₃N is more basic than C₆H₅CH₂NH₂. Thus, the given compounds can be arranged in the increasing order of their basic strengths as follows.