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Markownikoff rule

Also contains definition of: anti-Markownikoff addition

'In the addition of hydrogen halides to unsymmetrically constituted [unsaturated] hydrocarbons, the halogen atom becomes attached to the carbon bearing the lesser number of hydrogen atoms.' Originally formulated by Markownikoff (Markovnikov) to generalize the orientation in additions of hydrogen halides to simple alkenes, this rule has been extended to polar addition reactions as follows. 'In the heterolytic addition of a polar molecule to an alkene or alkyne, the more electronegative (nucleophilic) atom (or part) of the polar molecule becomes attached to the carbon atom bearing the smaller number of hydrogen atoms.' This is an indirect statement of the common mechanistic observation, that the more electropositive (electrophilic) atom (or part) of the polar molecule becomes attached to the end of the multiple bond that would result in the more stable carbenium ion (whether or not a carbenium ion is actually formed as a reaction intermediate in the addition reaction). Addition in the opposite sense is commonly called 'anti-Markovnikov addition'.
Source:
PAC, 1994, 66, 1077 (Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)) on page 1137
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IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. doi:10.1351/goldbook.
Last update: 2014-02-24; version: 2.3.3.
DOI of this term: doi:10.1351/goldbook.M03707.
Original PDF version: http://www.iupac.org/goldbook/M03707.pdf. The PDF version is out of date and is provided for reference purposes only. For some entries, the PDF version may be unavailable.
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