aldehyde ketones

aldehyde ketones
кетоалдехид

English-Bulgarian polytechnical dictionary . 2013.

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  • aldehyde — aldehydic, adj. /al deuh huyd /, n. Chem. any of a class of organic compounds containing the group CHO, which yields acids when oxidized and alcohols when reduced. [1840 50; < NL al(cohol) dehyd(rogenatum) dehydrogenated alcohol] * * * Any of a… …   Universalium

  • carboxylic acid — Chem. any organic acid containing one or more carboxyl groups. [1900 05; CARBOXYL + IC] * * * Any organic compound with the general chemical formula ―COOH in which a carbon (C) atom is bonded to an oxygen (O) atom by a double bond to make a… …   Universalium

  • Fehling's solution — is a solution used to differentiate between water soluble aldehyde and ketone functional groups, although ketose monosaccharides (such as fructose) will also test positive, due to conversion to aldoses by the base in the reagent [ [http://www.uni …   Wikipedia

  • Enol — Enols (also known as alkenols) are alkenes with a hydroxyl group affixed to one of the carbon atoms composing the double bond. Enols and carbonyl compounds (such as ketones and aldehydes) are in fact isomers; this is called keto enol… …   Wikipedia

  • organometallic compound — ▪ chemical compound Introduction  any member of a class of substances containing at least one metal to carbon bond in which the carbon is part of an organic group. Organometallic compounds constitute a very large group of substances that have… …   Universalium

  • Grignard reagent — Chem. any of the group of reagents produced by the interaction of magnesium and an organic halide, usually in the presence of an ether, and having the general formula RMgX, where R is an organic group and X is a halogen: used in the Grignard… …   Universalium

  • Aldol reaction — The aldol reaction is a powerful means of forming carbon–carbon bonds in organic chemistry.[1][2][3] Discovered independently by …   Wikipedia

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  • Wittig reaction — The Wittig reaction is a chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide (often called a Wittig reagent) to give an alkene and triphenylphosphine oxide. [cite journal author = Georg Wittig, Ulrich Schöllkopf journal …   Wikipedia

  • Alcohol oxidation — Mechanism of oxidation of primary alcohols to carboxylic acids via aldehydes and aldehyde hydrates Alcohol oxidation is an important organic reaction. Primary alcohols (R CH2 OH) can be oxidized either to aldehydes (R CHO) or to carboxylic acids… …   Wikipedia

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