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  2. Scholl reaction - Wikipedia

    en.wikipedia.org/wiki/Scholl_reaction

    The Scholl reaction is a coupling reaction between two arene compounds with the aid of a Lewis acid and a protic acid. [1] [2] It is named after its discoverer, Roland Scholl, a Swiss chemist. The Scholl reaction. In 1910 Scholl reported the synthesis of a quinone [3] and of perylene from naphthalene [4] both with aluminum chloride.

  3. Nucleic acid metabolism - Wikipedia

    en.wikipedia.org/wiki/Nucleic_acid_metabolism

    Nucleic acid metabolism is a collective term that refers to the variety of chemical reactions by which nucleic acids (DNA and/or RNA) are either synthesized or degraded. Nucleic acids are polymers (so-called "biopolymers") made up of a variety of monomers called nucleotides .

  4. Energy profile (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Energy_profile_(chemistry)

    Figure 6:Reaction Coordinate Diagrams showing reactions with 0, 1 and 2 intermediates: The double-headed arrow shows the first, second and third step in each reaction coordinate diagram. In all three of these reactions the first step is the slow step because the activation energy from the reactants to the transition state is the highest.

  5. Chemical oscillator - Wikipedia

    en.wikipedia.org/wiki/Chemical_oscillator

    In chemistry, a chemical oscillator is a complex mixture of reacting chemical compounds in which the concentration of one or more components exhibits periodic changes. They are a class of reactions that serve as an example of non-equilibrium thermodynamics with far-from-equilibrium behavior.

  6. Annulation - Wikipedia

    en.wikipedia.org/wiki/Annulation

    In organic chemistry, annulation (from Latin anellus 'little ring'; occasionally annelation) is a chemical reaction in which a new ring is constructed on a molecule. [ 1 ] Examples are the Robinson annulation , Danheiser annulation and certain cycloadditions .

  7. Prilezhaev reaction - Wikipedia

    en.wikipedia.org/wiki/Prilezhaev_reaction

    The reaction is highly stereospecific in the sense that the double bond stereochemistry is generally transferred to the relative configuration of the epoxide with essentially perfect fidelity, so that a trans-olefin leads to the stereoselective formation of the trans-2,3-substituted epoxide only, as illustrated by the example above, while a cis ...

  8. Ring-opening metathesis polymerisation - Wikipedia

    en.wikipedia.org/wiki/Ring-opening_metathesis...

    The reaction is driven by relieving ring strain in cyclic olefins. [2] A variety of heterogeneous and homogeneous catalysts have been developed for different polymers and mechanisms. [ 3 ] Heterogeneous catalysts are typical in large-scale commercial processes, while homogeneous catalysts are used in finer laboratory chemical syntheses. [ 4 ]

  9. Dehalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehalogenation

    In organic chemistry, dehalogenation is a set of chemical reactions that involve the cleavage of carbon-halogen bonds; as such, it is the inverse reaction of halogenation. Dehalogenations come in many varieties, including defluorination (removal of fluorine ), dechlorination (removal of chlorine ), debromination (removal of bromine ), and ...