Arrange the following in increasing order of basic strength:
`C_2H_5NH_2, (C_2H_5)_2NH,(C_2H_5)_3N,C_6H_5NH_2`

Arrange the following in increasing order of basic strength: CH_3NH_2, (CH_3)_2NH,(CH_3)_3N, C_6H_5CH_2NH_2

Arrange the following in increasing order of basic strength: C_2H_5NH_2, C_6H_5NH_2,NH_3,C_6H_5CH_2NH_2, and (C_2H_5)_2NH

Amines can be considered as derivatives of ammonia. Arrange the following in increasing order of their basic strength. C_6H_5NH_2,C_2H_5NH_2,(C_2H_5)_2NH,NH_3

Amines are basic. Arrange the following amines in the increasing order of base strength: CH_3NH_2, (CH_3)_2NH, (CH_3)_3N, C_6H_5NH_2

Arrange the following in increasing order of their basic strength: i) C_2 H_5 NH_2, C_6 H_5 NH_2, NH_3, C_6 H_5 CH_2 NH_2 and (C_2 H_5)_2 NH ii) C_2 H_5 NH_2, (C_2 H_5)_2 NH,(C_2 H_5)_3 N, C_6 H_5 NH_2 iii) CH_3 NH_2, (CH_3)_2 NH_4, (CH_3)_3 N, C_6 H_5 NH_2, C_6 H_5 CH_2 NH_2

Amines are basic. Arrange the following amines in the increasing order of base strength NH_3C_2H_5NH_2 , C_6H_5NH_2 , (C_2H_5)_2NH .

Aromatic and aliphatic amines are basic in nature like ammonia. Arrange the following compounds in the increasing order of their basic strngth: CH_3NH_2,(CH_3)_2NH,NH_3,C_6H_5-NH_2

Arrange the following in decreasing order of their bond angle ': H_2 O, NH_3, H_2 S'

S_N^1 reaction takes placed in two steps. The relative reactivity of an alkyl halide in S_N^1 reaction depends on the relative stability of carbocations formed by ionisation. Arrange the Following in decreasing order C_6H_5CH_2Br , C_6H_5CH(C_6H_5)Br , C_6H_5CH(CH_3)Br, C_6H_5C(CH_3)(C_6H_5)Br .