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Under common reaction conditions, a carb...

Under common reaction conditions, a carboncation rearranges to another carbocation of equal or greater stability. For example secondary carbocation will rearrange to a tertiary carbocation. It will not rearrange to a less stable primary carbocation. This generalization is not absolute, and because there is not is a high energy barrier to the rearrangement of carbocations, rearrangement to a less stable cation can occur if it offers the chance to forme a more stable product.
In the following cation , `H//CH_(3)` that is most likely to migarte to the positively charged carbon is :
`H_(3)C^(1)-^(2)underset(OH)underset(|)overset(H)overset(|)C-^(3)underset(H)underset(|)overset(o+)C-^(4)underset(CH_(3))underset(|)overset(H)overset(|)C-^(5)CH_(3)`

A

`CH_(3)"at"C-4`

B

`H"at"C-4`

C

`CH_(3)"at"C-2`

D

`H"at"C-2`

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The correct Answer is:
D

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Under common reaction conditions, a carboncation rearranges to another carbocation of equal or greater stability. For example secondary carbocation will rearrange to a tertiary carbocation. It will not rearrange to a less stable primary carbocation. This generalization is not absolute, and because there is not is a high energy barrier to the rearrangement of carbocations, rearrangement to a less stable cation can occur if it offers the chance to forme a more stable product. In which of the following cations rearrangement takes place?

Under common reaction conditions, a carboncation rearranges to another carbocation of equal or greater stability. For example secondary carbocation will rearrange to a tertiary carbocation. It will not rearrange to a less stable primary carbocation. This generalization is not absolute, and because there is not is a high energy barrier to the rearrangement of carbocations, rearrangement to a less stable cation can occur if it offers the chance to forme a more stable product. In which of the following cations rearrangement takes place most rapidly?

Rearrangement of Carbocations

Carbocation Rearrangement 1

Carbocation Rearrangement 2

Most stable carbocation is:

Most stable carbocation is:

Most stable carbocation is:

HIMANSHU PANDEY-GENERAL ORGANIC CHEMISTRY-Linked Comprehension Type (Q.1 To Q.25)
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  2. In an aromatic ring, a functional group with lone pair of electron exe...

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  3. In an aromatic ring, a functional group with lone pair of electron exe...

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  4. In an aromatic ring, a functional group with lone pair of electron exe...

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  5. The process whereby a hydrogen atom attached to the alpha-carbon of ca...

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  6. The process whereby a hydrogen atom attached to the alpha-carbon of ca...

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  7. The process whereby a hydrogen atom attached to the alpha-carbon of ca...

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  8. In which of the following cations rearrangement takes place?

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  9. Under common reaction conditions, a carboncation rearranges to another...

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  10. Under common reaction conditions, a carboncation rearranges to another...

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  11. Type of anios in which delocatisation of negative charge occrur on mor...

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  12. Type of anios in which delocatisation of negative charge occrur on mor...

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  13. Type of anios in which delocatisation of negative charge occrur on mor...

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  14. In a substance that are resonance hybirds, the measured length of give...

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  15. In a substance that are resonance hybirds, the measured length of give...

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  16. In a substance that are resonance hybirds, the measured length of give...

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  17. Basicity is defined by equilibrium constant for abstracting a proton. ...

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  18. Basicity is defined by equilibrium constant for abstracting a proton. ...

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  19. Basicity is defined by equilibrium constant for abstracting a proton. ...

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  20. Benzoic acid is more acidic than acetic acid, fomic acid is more acidi...

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