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  2. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    In discussing mechanisms of organic reactions, methyl lithium and related Grignard reagents are often considered to be salts of CH − 3; and though the model may be useful for description and analysis, it is only a useful fiction. Such reagents are generally prepared from the methyl halides: 2 M + CH 3 X → MCH 3 + MX. where M is an alkali metal.

  3. Carbon–hydrogen bond activation - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond...

    In this nickel-catalyzed process, methane is converted to the methyl substituent of coenzyme M, CH 3 SCH 2 CH 2 SO − 3. [24] Naturally occurring methane is not utilized as a chemical feedstock, despite its abundance and low cost. Current technology makes prodigious use of methane by steam reforming to produce syngas, a mixture of carbon ...

  4. Agostic interaction - Wikipedia

    en.wikipedia.org/wiki/Agostic_interaction

    The term agostic is reserved to describe two-electron, three-center bonding interactions between carbon, hydrogen, and a metal. Two-electron three-center bonding is clearly implicated in the complexation of H 2 , e.g., in W(CO) 3 (PCy 3 ) 2 H 2 , which is closely related to the agostic complex shown in the figure. [ 8 ]

  5. Pinacol coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Pinacol_coupling_reaction

    The pinacol coupling can be followed up by a pinacol rearrangement. A related reaction is the McMurry reaction , which uses titanium(III) chloride or titanium(IV) chloride in conjunction with a reducing agent for the formation of the metal-diol complex, and which takes place with an additional deoxygenation reaction step in order to provide an ...

  6. Oxidative addition - Wikipedia

    en.wikipedia.org/wiki/Oxidative_addition

    This mechanism applies to the addition of homonuclear diatomic molecules such as H 2. Many C–H activation reactions also follow a concerted mechanism through the formation of an M–(C–H) agostic complex. [2] A representative example is the reaction of hydrogen with Vaska's complex, trans-IrCl(CO)[P(C 6 H 5) 3] 2.

  7. Hydrogen auto-transfer - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_auto-transfer

    [1] [2] Mechanism of one type of carbonyl addition hydrogen auto-transfer reaction involving hydrometalation (step 2). [ 3 ] Hydrogen auto-transfer , also known as borrowing hydrogen , is the activation of a chemical reaction by temporary transfer of two hydrogen atoms from the reactant to a catalyst and return of those hydrogen atoms back to a ...

  8. Hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_bond

    An ubiquitous example of a hydrogen bond is found between water molecules. In a discrete water molecule, there are two hydrogen atoms and one oxygen atom. The simplest case is a pair of water molecules with one hydrogen bond between them, which is called the water dimer and is often used as a model system. When more molecules are present, as is ...

  9. Coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Coupling_reaction

    The most common type of coupling reaction is the cross coupling reaction. [ 1 ] [ 2 ] [ 3 ] Richard F. Heck , Ei-ichi Negishi , and Akira Suzuki were awarded the 2010 Nobel Prize in Chemistry for developing palladium-catalyzed cross coupling reactions .