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  2. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Schorigin Shorygin reaction, Shorygin reaction, Wanklyn reaction; Schotten–Baumann reaction; Seliwanoff's test; Semidine rearrangement; Semmler–Wolff reaction; Seyferth–Gilbert homologation; Shapiro reaction; Sharpless asymmetric dihydroxylation; Sharpless epoxidation [34] Sharpless oxyamination or aminohydroxylation; Shenck ene reaction ...

  3. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    is an alkaline solution of potassium permanganate; used in organic chemistry as a qualitative test for the presence of unsaturation, such as double bonds; N-Bromosuccinimide: used in radical substitution and electrophilic addition reactions in organic chemistry. Also acts as a mild oxidizer to oxidize benzylic or allylic alcohols.

  4. Organic reaction - Wikipedia

    en.wikipedia.org/wiki/Organic_reaction

    The oldest organic reactions are combustion of organic fuels and saponification of fats to make soap. Modern organic chemistry starts with the Wöhler synthesis in 1828. In the history of the Nobel Prize in Chemistry awards have been given for the invention of specific organic reactions such as the Grignard reaction in 1912, the Diels–Alder ...

  5. Category:Organic reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Organic_reactions

    Carbonyl α-substitution reaction; Carboxylation; Carbylamine reaction; Coarctate reaction; Concerted reaction; Conia-ene reaction; Copper-free click chemistry; Cracking (chemistry) Crich beta-mannosylation; Cycloisomerization

  6. Reformatsky reaction - Wikipedia

    en.wikipedia.org/wiki/Reformatsky_reaction

    The Reformatsky reaction (sometimes transliterated as Reformatskii reaction) is an organic reaction which condenses aldehydes or ketones with α-halo esters using metallic zinc to form β-hydroxy-esters: [1] [2] The Reformatsky reaction. The organozinc reagent, also called a 'Reformatsky enolate', is prepared by treating an alpha-halo ester ...

  7. Simmons–Smith reaction - Wikipedia

    en.wikipedia.org/wiki/Simmons–Smith_reaction

    The Simmons–Smith reaction is an organic cheletropic reaction involving an organozinc carbenoid that reacts with an alkene (or alkyne) to form a cyclopropane. [ 1 ] [ 2 ] [ 3 ] It is named after Howard Ensign Simmons, Jr. and Ronald D. Smith .

  8. Cope reaction - Wikipedia

    en.wikipedia.org/wiki/Cope_reaction

    (Rings with 5 or 7 or more members undergo the reaction just fine.) [6] [7] [8] This organic reaction is closely related to the Hofmann elimination, but the base is a part of the leaving group. Sulfoxides can undergo an essentially identical reaction to produce sulfenic acids, which is important in the antioxidant chemistry of garlic and other ...

  9. Glossary of chemistry terms - Wikipedia

    en.wikipedia.org/wiki/Glossary_of_chemistry_terms

    Also acid ionization constant or acidity constant. A quantitative measure of the strength of an acid in solution expressed as an equilibrium constant for a chemical dissociation reaction in the context of acid-base reactions. It is often given as its base-10 cologarithm, p K a. acid–base extraction A chemical reaction in which chemical species are separated from other acids and bases. acid ...