In organic chemistry, Markovnikov's rule or Markownikoff's rule describes the outcome of some addition reactions. The rule was formulated by Russian chemist Vladimir Markovnikov in 1870. …

Markovnikov’s rule is an empirical rule used to predict regioselectivity of electrophilic addition reactions of alkenes and alkynes. It states that, in hydrohalogenation of an unsymmetrical …

Feb 8, 2013 · The reaction tends to occur such that the halogen ends up attached to the carbon of the alkene attached to the fewest hydrogen atoms, a phenomenon known as Markovnikov’s Rule.

Markovnikov rule, in organic chemistry, a generalization, formulated by Vladimir Vasilyevich Markovnikov in 1869, stating that in addition reactions to unsymmetrical alkenes, the electron …

This preference for addition to alkenes was first explained by Markovnikov and is known as Markovnikov’s rule which states that: In the addition reaction of HX to an unsymmetrical …

Markovnikov Rule predicts the regiochemistry of HX addition to unsymmetrically substituted alkenes. The halide component of HX bonds preferentially at the more highly substituted …

After looking at the results of many such reactions, the Russian chemist Vladimir Markovnikov proposed in 1869 what has become known as: In the addition of HX to an alkene, the H …

Jul 23, 2025 · Markovnikov's Rule is a principle in organic chemistry that helps predict the outcome of an addition reaction when an unsymmetrical molecule reacts with a molecule …

Markovnikov’s rule helps predict the product of nucleophilic addition to alkenes. The nucleophile adds to the carbon with the highest degree (primary, secondary, etc.).

What is Markovnikov's Rule definition, explanation, Anti-Markovnikov's Rule mechanism, examples and pictures