In organic chemistry, a carbanion is an anion in which carbon is negatively charged.[failed verification] Formally, a carbanion is the conjugate base of...

chemical reaction used in organic chemistry of stabilized phosphonate carbanions with aldehydes (or ketones) to produce predominantly E-alkenes. In 1958...

centred on a carbon, it is termed a carbocation (if positively charged) or carbanion (if negatively charged). Monatomic ions are formed by the gain or loss...

(N≡CCH2–), a type of nitrile group The cyanomethyl radical (N≡CCH2·) The cyanomethyl carbanion (N≡CCH2−) Ethynyl Hydroxymethyl Trifluoromethyl v t e...

Because of the high polarity of the C-Na bonds, they behave like sources of carbanions (salts with organic anions). Some well-known derivatives include sodium...

Organomercury chemistry refers to the study of organometallic compounds that contain mercury. Typically the Hg–C bond is stable toward air and moisture...

Streitwieser, Jr., E. Juaristi, and L. L. Nebenzahl, in Comprehensive Carbanion Chemistry Volume 5: Part A Structure and Reactivity (Studies in Organic...

storage by amine gas treating. Only very strong nucleophiles, like the carbanions provided by Grignard reagents and organolithium compounds react with CO2...

nucleophilicity of the attacking nucleophile. Nucleophilic addition of a carbanion or another nucleophile to the double bond of an alpha, beta-unsaturated...

the right. A carbanion is a organic molecule where a carbon atom is not electron deficient but contain an overall negative charge. Carbanions are strong...