One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, SDS of cas: 20375-65-9, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 20375-65-9, Name is 3-Phenyl-6-chloropyridazine, molecular formula is C10H7ClN2
Stereoselective Micellar Catalysis. Part 3. Co-operative Effects of N-Decanoyl-L-histidine for the Hydrolysis of Enantiomeric Substrates
The catalytic activities of N-decanoyl-L-histidine (Ia) and its methyl ester (Ib) toward the hydrolyses of enantiomeric substrates (II) have been investigated in the presence of cetyltrimethylammonium bromide micelles.The comparison of catalytic effects (both the rate constants and stereoselectivities) of (Ia) and (Ib) strongly suggests that carboxylate ion of (Ia) intramolecularly enhances the reactivity of the imidazole group.The presence of co-operative effects is also supported by the pH-rate profile and by the thermodynamic parameters of the reaction.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. SDS of cas: 20375-65-9, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 20375-65-9, in my other articles.
Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N2653 – PubChem