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8.2 Hydrohalogenation of Alkenes | Organic Chemistry

Chad breaks down the hydrohalogenation of alkenes in which HCl, HBr, or HI is added across an alkene. Chad shows the step-by-step reaction mechanism for the addition of HBr to propene, explaining why it results in Markovnikov addition, has no stereoselectivity, and is subject to carbocation rearrangements. Chad then shows how the addition of HBr with peroxide (HBr/ROOR) proceeds through a radical mechanism resulting in anti-Markovnikov addition of HBr. If you want all my study guides, quizzes, and practice exams, check out my premium course at https://www.chadsprep.com/organic-che... 00:00 Lesson Introduction 01:08 Introduction to Hydrohalogenation 02:44 Hydrohalogenation of Alkenes Mechanism 05:09 Hydrohalogenation of Alkenes with peroxide (Addition of HBr / ROOR) https://www.chadsprep.com/

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