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  2. Addition reaction - Wikipedia

    en.wikipedia.org/wiki/Addition_reaction

    An addition reaction is the reverse of an elimination reaction, in which one molecule divides into two or more molecules. For instance, the hydration of an alkene to an alcohol is reversed by dehydration. There are two main types of polar addition reactions: electrophilic addition and nucleophilic addition.

  3. Reaction intermediate - Wikipedia

    en.wikipedia.org/wiki/Reaction_intermediate

    Carbocations are formed in two major alkene addition reactions. In an HX addition reaction, the pi bond of an alkene acts as a nucleophile and bonds with the proton of an HX molecule, where the X is a halogen atom. This forms a carbocation intermediate, and the X then bonds to the positive carbon that is available, as in the following two-step ...

  4. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction. The type of addition that occurs depends on multiple different factors of a reaction, and is defined by the final orientation of the substituents on the parent molecule.

  5. Kharasch addition - Wikipedia

    en.wikipedia.org/wiki/Kharasch_addition

    The Kharasch addition is an organic reaction and a metal-catalysed free radical addition of CXCl 3 compounds (X = Cl, Br, H) to alkenes. [1] The reaction is used to append trichloromethyl or dichloromethyl groups to terminal alkenes. The method has attracted considerable interest, [2] but it is of limited value because of narrow substrate scope ...

  6. Nucleophilic conjugate addition - Wikipedia

    en.wikipedia.org/.../Nucleophilic_conjugate_addition

    Nucleophilic conjugate addition is a type of organic reaction. Ordinary nucleophilic additions or 1,2-nucleophilic additions deal mostly with additions to carbonyl compounds. Simple alkene compounds do not show 1,2 reactivity due to lack of polarity , unless the alkene is activated with special substituents .

  7. Hydroamination - Wikipedia

    en.wikipedia.org/wiki/Hydroamination

    The addition of hydrogen and an amino group (NR 2) using reagents other than the amine HNR 2 is known as a "formal hydroamination" reaction. Although the advantages of atom economy and/or ready available of the nitrogen source are diminished as a result, the greater thermodynamic driving force, as well as ability to tune the aminating reagent ...

  8. Free-radical addition - Wikipedia

    en.wikipedia.org/wiki/Free-radical_addition

    [3]: 188, 751 The result is typically anti-Markovnikov addition, a phenomenon Morris Kharasch called the "peroxide effect". [4] Reaction is slower with alkynes than alkenes. [3]: 750 In the paradigmatic example, hydrogen bromide radicalyzes to monatomic bromine. These bromine atoms add to an alkene at the most accessible site, to give a ...

  9. Hydrocyanation - Wikipedia

    en.wikipedia.org/wiki/Hydrocyanation

    In organic chemistry, hydrocyanation is a process for conversion of alkenes to nitriles. The reaction involves the addition of hydrogen cyanide and requires a catalyst if the substrate alkene is unactivated. This conversion is conducted on an industrial scale for the production of precursors to nylon.

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