The correct order of the basic strength of methyl
substituted amines in aqueous solution is :
1 (CH3)2N>(CH3)2NH > CH3NH2
(2) CH3NH,> (CH3)2NH > (CH3)3N
(3) (CH3)2NH > CH3NH,> (CH3)3N
(4) (CH3)3N > CH3NH, > (CH3)2NH
Answers
Answered by
1
Answer:
SJJDJNJKNKKSDNDKFNGFJNHMFIEDRTCCC
Explanation:
Answered by
0
Answer:
In watery arrangement, electron giving inductive impact, solvation impact (H-holding) and steric block all together influence fundamental quality of substituted amines. At the point when amines are broken up in water, they structure protonated amines.
Likewise, the quantity of potential outcomes of hydrogen holding additionally increments. More the quantity of hydrogen holding, more is the hydration that is discharged during the time spent the arrangement of hydrogen bonds.
Similar questions