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11) Write the mechanism and predict the product for the following reaction, including stereochemistry: HBr
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→ Trignal ni it ? electron sich Carbocation Carboration [ More stable Idue to tI effect I ob BY - 스 You By t ing Major produc

Alkene are electron rich in nature it will attack the electrophilic part of HBr to form carbocation.

More stable is tertiary (3o) carbocation due to inductive effect of alkyl group. This carbocation will form the major product. As carbocation is sp​​​​​2​ hybridized which has trigonal planar geometry. It can be attacked by the nucleophile from both the sides. Hence form two stereoisomers.

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help for a thumbs up 11) Write the mechanism and predict the product for the following...
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