Chemistry, 01.07.2021 19:10 EricaLSH7624
According to Markovnikov's rule of the electrophilic addition to an alkene, the electrophile, usually a proton, is more likely to add to the less-substituted carbon in a double bond. This arrangement places the intermediate carbocation on the more-substituted carbon , which stabilizes it with the presence of . In the major product of a reaction following Markovnikov's rule, the . will then end up on the more-substituted carbon in a double bond.
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According to Markovnikov's rule of the electrophilic addition to an alkene, the electrophile, usuall...
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