- the reaction proceeds by the mechanism
- Макаров: реакция протекает по (такому-то) механизму
Универсальный англо-русский словарь. Академик.ру. 2011.
Универсальный англо-русский словарь. Академик.ру. 2011.
reaction mechanism — Introduction in chemical reactions (chemical reaction), the detailed processes by which chemical substances are transformed into other substances. The reactions themselves may involve the interactions of atoms (atom), molecules (molecule),… … Universalium
Reaction rate constant — In chemical kinetics a reaction rate constant k or λ quantifies the speed of a chemical reaction.[1] For a chemical reaction where substance A and B are reacting to produce C, the reaction rate has the form: Reaction: A + B → C k(T) is the… … Wikipedia
Heck reaction — The Heck reaction (also called the Mizoroki Heck reaction)[1] is the chemical reaction of an unsaturated halide (or triflate) with an alkene and a base and palladium catalyst to form a substituted alkene.[2][3] Together with the other palladium… … Wikipedia
Passerini reaction — The Passerini reaction is a chemical reaction involving an isocyanide, an aldehyde (or ketone), and a carboxylic acid to form a α acyloxy amide. [Passerini, M.; Simone, L. Gazz. Chim. Ital. 1921, 51 , 126 129.] [Passerini, M.; Ragni, G. Gazz.… … Wikipedia
Wulff-Dötz reaction — The Wulff Dötz reaction (also known as the Dötz reaction or the benzannulation reaction of the Fischer carbene complexes) is the chemical reaction of an aromatic or vinylic alkoxy pentacarbonyl chromium carbene complex with an alkyne and carbon… … Wikipedia
Suzuki reaction — The Suzuki reaction is the organic reaction of an aryl or vinyl boronic acid with an aryl or vinyl halide catalyzed by a palladium(0) complex. [Miyaura, N. et al. Tetrahedron Lett. 1979, 3437.] [Miyaura, N.; Suzuki, A. Chem. Commun. 1979, 866.]… … Wikipedia
E1cB elimination reaction — The E1cB elimination reaction is a special type of elimination reaction in organic chemistry. This reaction mechanism explains the formation of alkenes from (mostly) alkyl halides through a carbanion intermediate given specified reaction… … Wikipedia
Ugi reaction — The Ugi reaction is a multi component reaction in organic chemistry involving a ketone or aldehyde, an amine, an isocyanide and a carboxylic acid to form a bis amide. [cite journal | author = Ugi, I; Meyr, R.; Fetzer, U.; Steinbrückner, C. title … Wikipedia
Michaelis–Arbuzov reaction — The Michaelis–Arbuzov reaction (also called the Arbuzov reaction) is the chemical reaction of a trialkyl phosphite and an alkyl halide to form a phosphonate. The reaction was discovered by August Michaelis in 1898[1], and greatly explored by… … Wikipedia
Nierenstein reaction — The Nierenstein reaction is an organic reaction describing the conversion of an acid chloride into an haloketone with diazomethane.[1][2] It is an insertion reaction in that the methylene from the diazomethane is inserted into the carbon chlorine … Wikipedia
Grignard reaction — The Grignard reaction, named for the French chemist François Auguste Victor Grignard, is an organometallic chemical reaction in which alkyl or aryl magnesium halides (Grignard reagents), which act as nucleophiles, attack electrophilic carbon… … Wikipedia