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Organic chemistry has a strong tradition of naming a specific reaction to its inventor or inventors and a long list of so-called named reactions exists, conservatively estimated at 1000. A very old named reaction is the Claisen rearrangement (1912) and a recent named reaction is the Bingel reaction (1993).
Algar–Flynn–Oyamada reaction; Alkylimino-de-oxo-bisubstitution; Alkyne trimerisation; Alkyne zipper reaction; Allan–Robinson reaction; Allylic rearrangement; Amadori rearrangement; Amine alkylation; Angeli–Rimini reaction; Andrussov oxidation; Appel reaction; Arbuzov reaction, Arbusow reaction; Arens–Van Dorp synthesis, Isler ...
Although systematic approaches for naming reactions based on the reaction mechanism or the overall transformation exist, such as the IUPAC nomenclature for organic chemical transformations, these technically-descriptive names are often unwieldy or not specific enough, so people names are often more practical for efficient communication. [5]
Proposed concerted version of the Passerini reaction mechanism. This mechanism involves a trimolecular reaction between the isocyanide, carboxylic acid, and carbonyl in a sequence of nucleophilic additions. The reaction proceeds first through an imidate intermediate and then undergoes Mumm rearrangement to afford the Passerini product. [13] [14]
A simplified model of a chemical reaction with pathways for a light isotope (H) and heavy isotope (D) of hydrogen. The same principle applies for the light isotope 12 C and heavy isotope 13 C of carbon. The positions on the energy wells are based on the quantum harmonic oscillator. Note the lower energy state of the heavier isotope and the ...
During the night, a plant employing CAM has its stomata open, allowing CO 2 to enter and be fixed as organic acids by a PEP reaction similar to the C 4 pathway. The resulting organic acids are stored in vacuoles for later use, as the Calvin cycle cannot operate without ATP and NADPH, products of light-dependent reactions that do not take place ...
The IUPAC Nomenclature for Organic Chemical Transformations is a methodology for naming a chemical reaction.. Traditionally, most chemical reactions, especially in organic chemistry, are named after their inventors, the so-called name reactions, such as Knoevenagel condensation, Wittig reaction, Claisen–Schmidt condensation, Schotten–Baumann reaction, and Diels–Alder reaction.
Some plants have evolved mechanisms to increase the CO 2 concentration in the leaves under these conditions. [ 30 ] Plants that use the C 4 carbon fixation process chemically fix carbon dioxide in the cells of the mesophyll by adding it to the three-carbon molecule phosphoenolpyruvate (PEP), a reaction catalyzed by an enzyme called PEP ...