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ChemWiki: The Dynamic Chemistry Hypertext > Core > Organic Chemistry > Conjugation > Electrophilic Attack on Conjugated Dienes-Kinetic and Thermodynamic Control > Markovnikov Addition

Markovnikov Addition

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Markovnikov addition, also called Markovnikov's rule, states that a protic acid (HX) will add to an alkene such that the proton will bond to the less substituted carbon.


During this addition, the carbocation intermediate bares a positive charge on the most substituted carbon. The more substituted carbon, the more stable (tertiary > secondar > primary > methyl). If the reverse occurs, that is the more electronegative atom (X) ends up bonding to the least substituted carbon, it is termed anti-Markovnikov addition. The figure below shows a figure of both additions:



Fig. 1. Markovnikov and anti-Markovnikov additions of HBr to 1-methylcyclohexene.

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Last modified
18:43, 1 Oct 2013



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This material is based upon work supported by the National Science Foundation under Grant Numbers 1246120, 1525057, and 1413739.

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