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According to Markovnikov's rule:- Tertiary carbocation is most stable...so if there is a chance for the formation of Tertiary carbocation from a existing primary carbocation then the ion undergoes methyl and hydride shift to achieve a tertiary carbocation....
This is Markovnikov's rule
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➡️The rule states that with the addition of a protic acid HX to an asymmetric alkene, the acid hydrogen (H) gets attached to the carbon with more hydrogen substituents, and the halide (X) group gets attached to the carbon with more alkyl substituents. ☯️☣️
➡️Alternatively, the rule can be stated that the hydrogen atom is added to the carbon with the greatest number of hydrogen atoms while the X component is added to the carbon with the least number of hydrogen atoms.☯️☣️
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utkarsh61412:
thank you
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