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  2. Deprotonation - Wikipedia

    en.wikipedia.org/wiki/Deprotonation

    Deprotonation (or dehydronation) is the removal (transfer) of a proton (or hydron, or hydrogen cation), (H +) from a Brønsted–Lowry acid in an acid–base reaction. [ 1 ] [ 2 ] The species formed is the conjugate base of that acid.

  3. Concerted metalation deprotonation - Wikipedia

    en.wikipedia.org/wiki/Concerted_metalation...

    Concerted metalation-deprotonation (CMD) is a mechanistic pathway through which transition-metal catalyzed C–H activation reactions can take place. In a CMD pathway, the C–H bond of the substrate is cleaved and the new C–Metal bond forms through a single transition state . [ 1 ]

  4. Hexane - Wikipedia

    en.wikipedia.org/wiki/Hexane

    Hexane and other volatile hydrocarbons (petroleum ether) present an aspiration risk. [26] n-Hexane is sometimes used as a denaturant for alcohol, and as a cleaning agent in the textile, furniture, and leather industries. It is slowly being replaced with other solvents. [27] Like gasoline, hexane is highly volatile and is an explosion risk.

  5. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    deprotonation of the carbocation. E1 typically takes place with tertiary alkyl halides, but is possible with some secondary alkyl halides. The reaction rate is influenced only by the concentration of the alkyl halide because carbocation formation is the slowest step, as known as the rate-determining step .

  6. Protonation - Wikipedia

    en.wikipedia.org/wiki/Protonation

    Protonation and deprotonation (removal of a proton) occur in most acid–base reactions; they are the core of most acid–base reaction theories. A Brønsted–Lowry acid is defined as a chemical substance that protonates another substance.

  7. Hammett equation - Wikipedia

    en.wikipedia.org/wiki/Hammett_equation

    The starting point for the collection of the substituent constants is a chemical equilibrium for which the substituent constant is arbitrarily set to 0 and the reaction constant is set to 1: the deprotonation of benzoic acid or benzene carboxylic acid (R and R' both H) in water at 25 °C. Scheme 1. Dissociation of benzoic acids

  8. Dehydrogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrogenation

    In chemistry, dehydrogenation is a chemical reaction that involves the removal of hydrogen, usually from an organic molecule.It is the reverse of hydrogenation. ...

  9. n-Butyllithium - Wikipedia

    en.wikipedia.org/wiki/N-Butyllithium

    The stability and volatility of the butane resulting from such deprotonation reactions is convenient, but can also be a problem for large-scale reactions because of the volume of a flammable gas produced. LiC 4 H 9 + RH → C 4 H 10 + RLi. The kinetic basicity of n-BuLi is affected by the solvent or cosolvent.