Markovnikov's rule

From WikiMD's Wellness Encyclopedia

Markovnikov's Rule is a fundamental principle in organic chemistry that predicts the outcome of the addition of hydrogen halides (HX, where X is a halogen) to alkenes and alkynes. This rule, named after the Russian chemist Vladimir Markovnikov, helps in determining the regioselectivity of such addition reactions. Understanding Markovnikov's Rule is crucial for chemists to synthesize desired organic compounds with precision.

Overview[edit | edit source]

Markovnikov's Rule states that in the addition of a protic acid (HX) to an unsymmetrical alkene or alkyne, the hydrogen (H) atom from the acid will add to the carbon atom with the greater number of hydrogen atoms, and the halide (X) will add to the carbon atom with fewer hydrogen atoms. This rule is often summarized by the phrase "the rich get richer," indicating that the more substituted carbon (the carbon with more carbon atoms attached) will receive the halide atom.

Mechanism[edit | edit source]

The mechanism underlying Markovnikov's Rule involves the formation of a more stable carbocation intermediate. When a protic acid is added to an unsymmetrical alkene, the double bond breaks, and a carbocation is formed on the more substituted carbon atom because it is more stable due to inductive effects and hyperconjugation. This increased stability makes the reaction pathway leading to this carbocation more favorable, thus dictating the regiochemistry of the addition.

Exceptions[edit | edit source]

While Markovnikov's Rule provides a general guideline for predicting the outcome of addition reactions, there are exceptions. For instance, the presence of peroxides in the reaction of hydrogen bromide (HBr) with alkenes leads to anti-Markovnikov addition, where the bromine atom adds to the more substituted carbon. This exception is explained by the radical substitution mechanism, known as the peroxide effect or Kharasch effect.

Applications[edit | edit source]

Markovnikov's Rule is widely applied in the synthesis of various organic compounds, including alcohols, halides, and ethers. It is particularly useful in the pharmaceutical and petrochemical industries, where the selective synthesis of compounds is essential.

Related Concepts[edit | edit source]

See Also[edit | edit source]

WikiMD
Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD

Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD