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In the case where the heterochiral complexes ML R L R L S and ML S L S L R are less reactive than the homochiral complexes ML S L S L S and ML R L R L R, a kinetic behavior similar to the ML 2 model is observed (Figure 9). However, a substantially different behavior is observed in the case where the heterochiral complexes are more reactive than
Additionally, the reactivity of two series of ketones are in the orders Cl 3 CCOCH 3 > CH 3 COCH 3 > C 6 H 5 COCH 3 and cyclohexanone > cyclopentanone > cycloheptanone > cyclooctanone. [7] [8] These orders of reactivity are the same as those observed for reactions that are well established as proceeding through nucleophilic attack on a carbonyl ...
There are three common types of chemical reaction where normality is used as a measure of reactive species in solution: In acid-base chemistry, normality is used to express the concentration of hydronium ions (H 3 O +) or hydroxide ions (OH −) in a solution. Here, 1 / f eq is an integer value. Each solute can produce one or more ...
Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene.These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative.
The Curtin–Hammett principle is a principle in chemical kinetics proposed by David Yarrow Curtin and Louis Plack Hammett.It states that, for a reaction that has a pair of reactive intermediates or reactants that interconvert rapidly (as is usually the case for conformational isomers), each going irreversibly to a different product, the product ratio will depend both on the difference in ...
Benzene is converted to cyclohexylbenzene by acid-catalyzed alkylation with cyclohexene. [6] Cyclohexylbenzene is a precursor to both phenol and cyclohexanone. [7]Hydration of cyclohexene gives cyclohexanol, which can be dehydrogenated to give cyclohexanone, a precursor to caprolactam.
A corollary of the effect is to explain the existence of one-way enzymes that are much more effective catalysts for one direction of reaction than the other. For example, the limiting rate in the forward direction of the reaction catalyzed by methionine adenosyltransferase is about 2 × 10 5 times higher than it is for the reverse reaction. [5]
Chemoselectivity is the preferential reaction of a chemical reagent with one of two or more different functional groups. [1]In a chemoselective system, a reagent in the presence of an aldehyde and an ester would mostly target the aldehyde, even if it has the option to react with the ester.