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  2. Trimethylsilyl iodide - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_iodide

    Trimethylsilyl iodide is used to introduce the trimethylsilyl group onto alcohols (ROH): . R-OH + TMSI → R-OTMS + HI. This type of reaction may be useful for gas chromatography analysis; the resultant silyl ether is more volatile than the underivatized original materials. [4]

  3. Outline of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Outline_of_organic_chemistry

    The following outline is provided as an overview of and topical guide to organic chemistry: . Organic chemistry is the scientific study of the structure, properties, composition, reactions, and preparation (by synthesis or by other means) of carbon-based compounds, hydrocarbons, and their derivatives.

  4. Methanesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonyl_chloride

    Methanesulfonyl chloride is mainly used to give methanesulfonates by its reaction with alcohols in the presence of a non-nucleophilic base. [8] In contrast to the formation of toluenesulfonates from alcohols and p-toluenesulfonyl chloride in the presence of pyridine, the formation of methanesulfonates is believed to proceed via a mechanism wherein methanesulfonyl chloride first undergoes an ...

  5. Organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Organic_chemistry

    Organic chemistry is a subdiscipline within chemistry involving the scientific study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms. [1]

  6. Organic reaction - Wikipedia

    en.wikipedia.org/wiki/Organic_reaction

    Organic chemistry has a strong tradition of naming a specific reaction to its inventor or inventors and a long list of so-called named reactions exists, conservatively estimated at 1000. A very old named reaction is the Claisen rearrangement (1912) and a recent named reaction is the Bingel reaction (1993).

  7. Nomenclature of Organic Chemistry - Wikipedia

    en.wikipedia.org/wiki/Nomenclature_of_Organic...

    A full edition was published in 1979, [1] an abridged and updated version of which was published in 1993 as A Guide to IUPAC Nomenclature of Organic Compounds. [2] Both of these are now out-of-print in their paper versions, but are available free of charge in electronic versions.

  8. Organic synthesis - Wikipedia

    en.wikipedia.org/wiki/Organic_synthesis

    Organic synthesis is an important chemical process that is integral to many scientific fields. Examples of fields beyond chemistry that require organic synthesis include the medical industry, pharmaceutical industry, and many more. Organic processes allow for the industrial-scale creation of pharmaceutical products.

  9. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    In chemistry, absolute configuration refers to the spatial arrangement of atoms within a molecular entity (or group) that is chiral, and its resultant stereochemical description. [1] Absolute configuration is typically relevant in organic molecules where carbon is bonded to four different substituents .