1.

Arrange the following carbocations in order of increasing stability I. (CH_(3))_(3)C CH_(2)^(+)II. (CH_(3))_(3)C^(+) III. CH_(3)CH_(2)CH_(2)^(+)IV. CH_(3)-overset(+)(C)H - CH_(3)

Answer»

`IV lt III lt II lt I`
`III lt IV lt I lt II`
`I lt III lt IV lt II`
`II lt IV lt III lt I`

Solution :`(CH_(3))_(3)OVERSET(+)(C)` (II) is stabilized by nine, `CH_(3)overset(+)(C)HCH_(3)(IV)` is stabilized by SIX, `CH_(3)CH_(2)CH_(2)^(+)` (III) is stabilized by twowhile `(CH_(3))_(3)C CH_(2)^(+)` (I) has no hyperconjugation structure. Therefore, II is the most stable, followed IV, then by III while I is the least stable. Thus, option (c) is CORRECT.


Discussion

No Comment Found