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  2. Markovnikov's rule - Wikipedia

    en.wikipedia.org/wiki/Markovnikov's_rule

    Such reactions are said to be anti-Markovnikov, since the halogen adds to the less substituted carbon, the opposite of a Markovnikov reaction. The anti-Markovnikov rule can be illustrated using the addition of hydrogen bromide to isobutylene in the presence of benzoyl peroxide or hydrogen peroxide. The reaction of HBr with substituted alkenes ...

  3. Oxymercuration reaction - Wikipedia

    en.wikipedia.org/wiki/Oxymercuration_reaction

    The reaction follows Markovnikov's rule (the hydroxy group will always be added to the more substituted carbon). The oxymercuration part of the reaction involves anti addition of OH group but the demercuration part of the reaction involves free radical mechanism and is not stereospecific, i.e. H and OH may be syn or anti to each other.

  4. Markov's principle - Wikipedia

    en.wikipedia.org/wiki/Markov's_principle

    Anne Troelstra [2] proved that it is an admissible rule in Heyting arithmetic. Later, the logician Harvey Friedman showed that Markov's rule is an admissible rule in first-order intuitionistic logic , Heyting arithmetic , and various other intuitionistic theories, [ 3 ] using the Friedman translation .

  5. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    The reaction is considered Markovnikov as it results in water addition with same regiospecificity as a direct hydration reaction. Alkene hydroboration-oxidation: Stereospecific: Can only be syn addition – hydrogen and hydroxyl (-OH) are added to the same face. The reaction is anti-Markovnikov. Hydroxyl attaches to the less substituted carbon.

  6. Hydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrohalogenation

    In the presence of peroxides, HBr adds to a given alkene in an anti-Markovnikov addition fashion. Regiochemistry follows from the reaction mechanism, which exhibits halogen attack on the least-hindered unsaturated carbon.

  7. Morris S. Kharasch - Wikipedia

    en.wikipedia.org/wiki/Morris_S._Kharasch

    In 1869, a Russian chemist named Vladimir Markovnikov demonstrated that the addition of HBr to alkenes usually but not always resulted in a specific orientation. Markovnikov's rule, which stems from these observations, states that in the addition of HBr or another hydrogen halide to an alkene, the acidic proton will add to the less substituted carbon of the double bond. [3]

  8. Markov chain - Wikipedia

    en.wikipedia.org/wiki/Markov_chain

    For example, the transition probabilities from 5 to 4 and 5 to 6 are both 0.5, and all other transition probabilities from 5 are 0. These probabilities are independent of whether the system was previously in 4 or 6. A series of independent states (for example, a series of coin flips) satisfies the formal definition of a Markov chain.

  9. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Markovnikov's rule, Markownikoff rule, Markownikow rule; Marschalk reaction; Martinet dioxindole synthesis; McDougall monoprotection; McFadyen–Stevens reaction; McMurry reaction; Meerwein arylation; Meerwein–Ponndorf–Verley reduction; Meisenheimer rearrangement; Meissenheimer complex; Menshutkin reaction; Metal-ion-catalyzed σ-bond ...