How can inductive and hyperconjugation effect explain the stability of primary, secondary and tertiary carbocations. Draw the orbital diagram for methyl carbocation indicating the shape and hybridization involved.
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Answer:The stability of carbocations increases as we go from primary to secondary to tertiary carbons. ... The second, (and theoretically more satisfactory explanation) is hyperconjugation, which invokes stabilization through donation of the electrons in C-H sigma bonds to the empty p orbital of the carbocation.
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