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Alkenes undergo electrophilic addition reactions due to their electron-rich C=C double bonds, forming carbocation intermediates that vary in stability based on the number of alkyl groups attached. Tertiary carbocations are the most stable, leading to the formation of the main product from the more stable carbocation. The document outlines specific reactions of alkenes with Br2, HBr, H2SO4, and H2O, detailing the mechanisms and examples for each reaction.

Author

Yusuf Ramzeen

Language

EN