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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.
This category was created to provide a "home" for inorganic compounds (such as NaBH 4) that are widely used in stoichiometric quantities in organic chemistry, but widely used organic reagents (such as oxalyl chloride) may belong here also. This category is not for catalysts such as Pd.
Well-known reactions and reagents in organic chemistry include 0-9. 1,2-Wittig rearrangement ...
The online version is also known as e-EROS. The encyclopedia contains a description of the use of reagents used in organic chemistry. [1] [2] The eight-volume print version includes 3500 alphabetically arranged articles and the online version is regularly updated to include new reagents and catalysts.
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).
Reagents for organic chemistry (10 C, 227 P) Pages in category "Reagents" The following 6 pages are in this category, out of 6 total. This list may not reflect recent ...
Chemistry portal Wikimedia Commons has media related to Organic reactions . This category encompasses the organic reaction archetype, and includes organic name reactions.
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.
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