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  2. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Download as PDF; Printable version ... Well-known reactions and reagents in organic chemistry include 0-9. 1,2-Wittig rearrangement ... Free radical halogenation ...

  3. Category:Organic reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Organic_reactions

    Download as PDF; Printable version; ... This category encompasses the organic reaction archetype, ... Conia-ene reaction; Copper-free click chemistry;

  4. File:Organic chemistry for advanced students (IA ...

    en.wikipedia.org/wiki/File:Organic_chemistry_for...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Donate; Pages for logged out editors learn more

  5. IUPAC nomenclature for organic chemical transformations

    en.wikipedia.org/wiki/IUPAC_nomenclature_for...

    The IUPAC Nomenclature for Organic Chemical Transformations is a methodology for naming a chemical reaction.. Traditionally, most chemical reactions, especially in organic chemistry, are named after their inventors, the so-called name reactions, such as Knoevenagel condensation, Wittig reaction, Claisen–Schmidt condensation, Schotten–Baumann reaction, and Diels–Alder reaction.

  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. Riley oxidation - Wikipedia

    en.wikipedia.org/wiki/Riley_oxidation

    Allylic oxidation can be predicted by the substitution pattern on the olefin. In the case of 1,2-disubstituted olefins, reaction rates follow CH > CH 2 > CH 3: Geminally-substituted olefins react in the same order of reaction rates as above: [2] Trisubstituted alkenes experience reactivity at the more substituted end of the double bond.

  8. Claisen–Schmidt condensation - Wikipedia

    en.wikipedia.org/wiki/Claisen–Schmidt_condensation

    Quantitative yields in Claisen–Schmidt reactions have been reported in the absence of solvent using sodium hydroxide as the base and plus benzaldehydes. [5] Because the enolizable nucleophilic carbonyl compound and the electrophilic carbonyl compound are two different chemicals, the Claisen–Schmidt reaction is an example of a crossed aldol ...

  9. Name reaction - Wikipedia

    en.wikipedia.org/wiki/Name_reaction

    A name reaction (or named reaction) is a chemical reaction named after its discoverer(s) or developer(s). Among the tens of thousands of organic reactions that are known, hundreds of such reactions are typically identified by the eponym . [ 1 ]