aliphatic aldehydes

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

• Aldehyde — An aldehyde. Formaldehyde, the simplest aldehyde …   Wikipedia

• Коптюг — Коптюг, Валентин Афанасьевич Валентин Афанасьевич Коптюг Дата рождения: 9 июня 1931(1931 06 09) Место рождения: Юхнов, Западная область, СССР Дата смерти: 10 января 1997 …   Википедия

• 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

• Meyers synthesis — The Meyers synthesis is an organic synthesis for the preparation of unsymmetrical aldehydes via hydrolysis of an oxazine [1][2][3][4]. The reaction is named after the American chemist Albert I. Meyers …   Wikipedia

• Meyers-Synthese — Die Meyers Synthese ist eine organisch chemische Reaktion zur Herstellung von Aldehyden durch die Hydrolyse eines Oxazins.[1][2][3] [4] Die Reaktion ist benannt nach ihrem Entdecker, dem amerikanischen Chemiker Albert I. Meyers. Reaktionsverlauf… …   Deutsch Wikipedia

• Schiff base — shif also Schiff s base n any of a class of bases of the general formula RR C=NR that are obtained typically by condensation of an aldehyde or ketone with a primary amine (as aniline) with elimination of water, that usu. polymerize readily if… …   Medical dictionary

• Incense — Burning incense Incense (from Latin: incendere, to burn )[1] is composed of aromatic biotic materials, which release fragrant smoke when burned. The term incense refers to the substance itself, rather than to the odor that it produces. It is used …   Wikipedia

• tautomerism — tautomeric /taw teuh mer ik/, adj. /taw tom euh riz euhm/, n. Chem. the ability of certain organic compounds to react in isomeric structures that differ from each other in the position of a hydrogen atom and a double bond. [1880 85; TAUTO +… …   Universalium

• Horner-Wadsworth-Emmons reaction — The Horner Wadsworth Emmons reaction (or HWE reaction) is the chemical reaction of stabilized phosphonate carbanions with aldehydes (or ketones) to produce predominantly E alkenes.In 1958, Leopold Horner published a modified Wittig reaction using …   Wikipedia

• Получение спиртов — Основная статья: Спирты Спирты являются обширным и очень разнообразным классом органических соединений: они широко распространены в природе, имеют важнейшее промышленное значение и обладают исключительными химическими свойствами. Существует… …   Википедия