Advertisements
Advertisements
प्रश्न
Give reason (CH3)2NH is more basic than (CH3)3N in an aqueous solution.
Advertisements
उत्तर
With the increase in the alkyl group, the +I effect will increase which will increase the ease of donation of lone pair electron. But in water, one other factor is controlling the strength of basicity.
Amine will accept a proton and form the cation. This cation will be stabilised in water by solvation (by hydrogen bonding). Better the solvation by hydrogen bonding, higher will be the basic strength.

Thus with the increase in methyl group, hydrogen bonding and stabilisation by solvation decreases. The net effect is when we move from secondary to tertiary amine basic strength actually decreases.
APPEARS IN
संबंधित प्रश्न
Arrange the following: C2H5NH2, C2H5OH, (CH3)3N – in the increasing order of their boiling point
Arrange the following in increasing order of their basic strength :

How will you convert Benzene into aniline?
How will you convert Benzene into N, N-dimethylaniline?
Arrange the following in the increasing order of their pKb values:
C6H5NH2, C2H5NH2, C6H5NHCH3
Illustrate the following reactions giving suitable example in each case
Ammonolysis
Arrange the following in increasing order of basic strength :
C6H5NH2, C6H5NHCH3, C6H5N(CH3)2
Tertiary amines have lowest boiling points because ________________
Among the following isomeric amines, an amine having highest boiling point is:
Assertion: N-Ethylbenzene sulphonamide is soluble in alkali.
Reason: Hydrogen attached to nitrogen in sulphonamide is strongly acidic.
