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See all on WikipediaMarkovnikov's rule - Wikipedia
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. See more
The rule states that with the addition of a protic acid HX or other polar reagent to an asymmetric alkene, the acid hydrogen (H) or electropositive … See more
• Markovnikov's rule and carbocations – Khan Academy. 25 August 2010. See more
Also called Kharasch effect (named after Morris S. Kharasch), these reactions that do not involve a carbocation intermediate may react through … See more
Wikipedia text under CC-BY-SA license Markovnikov's Rule
WEBFeb 7, 2019 · Markovnikov’s Rule, also known as Markownikoff’s rule, can be used to describe the outcome of some chemical addition reactions. The Russian chemist …
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Markovnikov’s Rule - Chemistry LibreTexts
WEBFeb 28, 2022 · 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 alkene, …
10.10: Markovnikov’s Rule - Chemistry LibreTexts
WEBThis rule of thumb is known as Markovnikov's rule, after the Russian chemist Vladimir Markovnikov who proposed it in 1869. While it is useful in many cases, Markovikov's …
7.8 Orientation of Electrophilic Additions: Markovnikov’s Rule
WEBMarkovnikov’s rule. In the addition of HX to an alkene, the H attaches to the carbon with fewer alkyl substituents and the X attaches to the carbon with more alkyl substituents. …
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Markovnikov's Rule - Organic Chemistry Portal
WEBMarkovnikov Rule predicts the regiochemistry of HX addition to unsymmetrically substituted alkenes. The halide component of HX bonds preferentially at the more highly substituted …
Markovnikov rule | Addition of Hydrogen, Alkenes, Alkanes
WEBMarkovnikov rule, in organic chemistry, a generalization, formulated by Vladimir Vasilyevich Markovnikov in 1869, stating that in addition reactions to unsymmetrical alkenes, the …
7.9: Orientation of Electrophilic Additions
WEBMarkovnikov's rule: During the electrophilic addition of HX to an alkene, the H adds to the carbon of the double bond with the fewest number of alkyl substitutent. The halide (X) adds to the double bond carbon with the …
3.2.11 Markovnikov's Rule - Save My Exams
WEBMar 2, 2011 · The nucleophile ends up to the most substituted C-C carbon atom. This is also known as the Markovnikov’s rule which predicts the outcome of addition reactions …
Markovnikov's rule and carbocations (video) | Khan Academy
WEBMarkovnikov's rule and carbocations (video) | Khan Academy. Science > Organic chemistry > Alkenes and alkynes > Alkene reactions. Markovnikov's rule and carbocations. …
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