Define markonikovs rule and briefly explain

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Markovnikov's rule, also known as Markovnikov's law, is a concept in organic chemistry that predicts the regioselectivity of electrophilic addition reactions of asymmetrical alkenes or alkynes. It states that when a protic acid (such as HX) adds to an unsymmetrical alkene, the hydrogen (H) from the protic acid preferentially attaches itself to the carbon atom with the greater number of hydrogen atoms bonded to it. The halogen or other substituent in the protic acid attaches itself to the other carbon atom of the alkene.

In simpler terms, Markovnikov's rule suggests that the hydrogen atom of the acid adds to the carbon atom in the alkene that already has more hydrogen atoms attached to it. This rule was formulated by the Russian chemist Vladimir Markovnikov in the 19th century based on experimental observations. It is widely used to predict the outcome of addition reactions involving alkenes and alkynes and has significant implications in the synthesis of organic compounds.
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