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[1] [2] It was originally developed at the Royal Society of Chemistry (RSC) and is associated with the Open Biomedical Ontologies Foundry. The RXNO ontology unifies several previous attempts to systematize chemical reactions including the Merck Index and the hierarchy of Carey, Laffan, Thomson and Williams.
This can be economically viable if the products can be separated and both have a value; the commercial conversion of furfural into furfuryl alcohol and 2-furoic acid is an example of this. [6] Alternatively, higher yields of one product (usually the alcohol) can be achieved in the crossed Cannizzaro reaction , in which a sacrificial aldehyde is ...
Cadiot–Chodkiewicz coupling; Cadogan-Sundberg indole synthesis; Camps quinoline synthesis; Cannizzaro reaction; Carbohydrate acetalisation; Carbonyl reduction
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
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 alliums. Selenoxides likewise undergo selenoxide eliminations.
Associative substitution describes a pathway by which compounds interchange ligands. The terminology is typically applied to organometallic and coordination complexes, but resembles the Sn2 mechanism in organic chemistry. The opposite pathway is dissociative substitution, being analogous to the Sn1 pathway. Intermediate pathways exist between ...
List of compounds; List of organic compounds; List of proteins This page was last edited on 20 February 2025, at 00:04 (UTC). Text is available under the ...
In organic chemistry, an oxime is an organic compound belonging to the imines, with the general formula RR’C=N−OH, where R is an organic side-chain and R' may be hydrogen, forming an aldoxime, or another organic group, forming a ketoxime. O-substituted oximes form a closely related family of compounds.