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organic compound; often used as a foamer in plastics and rubber and as a radical initiator: Baeyer's reagent: 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
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.
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
S N 1; S N 2; S N i; Solvolysis; Sommelet reaction; Sonn–Müller method; Sonogashira coupling; Sørensen formol titration; Staedel–Rugheimer pyrazine synthesis; Stahl oxidation; Staudinger reaction; Staudinger synthesis; Steglich esterification; Stephen aldehyde synthesis; Stephens-Castro coupling; Stetter reaction; Stevens rearrangement ...
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]
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.
6 Organic chemistry. Toggle Organic chemistry subsection. 6.1 Prefixes for naming carbon chains. 6.2 Carboxylic acids. 6.3 Dicarboxylic acids. 6.4 Aromatic compounds.
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).