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Explain the stability of tert-butyl cation, isopropyl cation, ethyl cation and methyl cation on the basis of hyperconjugation.

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i. Greater the number of alkyl groups attached to a positively charged carbon atom, more is the number of α-hydrogens, more is the hyperconjugation structures and more is the stability of the cation.

ii. Thus, the relative stability of the cations decreases in the order:

3° carbocation > 2° carbocation > 1° carbocation > Methyl cation

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