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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. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    In organic chemistry, an acetyl group is a functional group denoted by the chemical formula −COCH 3 and the structure −C(=O)−CH 3. It is sometimes represented by the symbol Ac [5] [6] (not to be confused with the element actinium). In IUPAC nomenclature, an acetyl group is called an ethanoyl group.

  4. Kolbe electrolysis - Wikipedia

    en.wikipedia.org/wiki/Kolbe_electrolysis

    Another example is the synthesis of 2,7-dimethyl-2,7-dinitrooctane from 4-methyl-4-nitrovaleric acid: [3] The Kolbe reaction has also been occasionally used in cross-coupling reactions . In 2022, it was discovered that the Kolbe electrolysis is enhanced if an alternating square wave current is used instead of a direct current .

  5. Geminal - Wikipedia

    en.wikipedia.org/wiki/Geminal

    In 1 H NMR spectroscopy, the coupling of two hydrogen atoms on the same carbon atom is called a geminal coupling. It occurs only when two hydrogen atoms on a methylene group differ stereochemically from each other. The geminal coupling constant is referred to as 2 J since the hydrogen atoms couple through two bonds. Depending on the other ...

  6. 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 ...

  7. 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 ]

  8. Isolobal principle - Wikipedia

    en.wikipedia.org/wiki/Isolobal_principle

    For example, methane is a simple molecule from which to form a main group fragment. The removal of a hydrogen atom from methane generates a methyl radical. The molecule retains its molecular geometry as the frontier orbital points in the direction of the missing hydrogen atom. Further removal of hydrogen results in the formation of a second ...

  9. Methyl radical - Wikipedia

    en.wikipedia.org/wiki/Methyl_radical

    Methyl radical is an organic compound with the chemical formula CH • 3 (also written as [CH 3] •). It is a metastable colourless gas, which is mainly produced in situ as a precursor to other hydrocarbons in the petroleum cracking industry. It can act as either a strong oxidant or a strong reductant, and is quite corrosive to metals.