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Reaction rates, of hydrolysis

Influence of the Monovalent Ions. The addition of ammonium salts retard the course of the deesterification by changing the reaction rate of hydrolysis and ammonolysis. By increasing the concentration of the ions the conversion of the ester groups is reduced from 83.3 % for 0,01 M to 62.8 % for 0.2 M (without added salt this value is 84.05 %), and the ratio hydrolysis ammonolysis is changed correspondingly from 53.8 76.2 to 37.3 62.7 (without added salt this ratio is 57.6 42.4). [Pg.531]

These results were supported by the hydrolysis rate at various water concentrations. These experiments clearly showed that the water concentration and the reaction rate of hydrolysis were not proportional. Furthermore, the methanolysis of the a -acetates provided the corresponding a - methoxy nitrosamines (result of C - O bond fission) and not methyl acetate. [Pg.66]

Eadie (1942) measured the initial reaction rate of hydrolysis of acetylcholme (substrate) by dog serum (source of enzyme) and obtained the following data ... [Pg.42]

Fig. 18 Reaction rate of hydrolysis of p-nitrophenyl acetate as a function of inverse temperature. Thermosensitive imidazole-containing copolymers (PVCL-Vim, PNIPA-Vim), 1-methylimidazole and poly(l-vinylimidazole) act as catalysts. Numbers in the copolymer abbreviations denote the Vim content (in mole percent). Vim 1-vinylimidazole. (Adapted from Ref. [18])... Fig. 18 Reaction rate of hydrolysis of p-nitrophenyl acetate as a function of inverse temperature. Thermosensitive imidazole-containing copolymers (PVCL-Vim, PNIPA-Vim), 1-methylimidazole and poly(l-vinylimidazole) act as catalysts. Numbers in the copolymer abbreviations denote the Vim content (in mole percent). Vim 1-vinylimidazole. (Adapted from Ref. [18])...
Relative reaction rates of hydrolysis, condensation, reesterification, and dissolution must be understood and controlled to dictate structural evolution. However, accurate values for rate constants are difficult to obtain because of the enormous number of distinguishable reactions as next nearest neighbors are considered, and to the concurrency of these reactions. Assink and Kay [45] use a simplified statistical model assuming that the local silicon environment does not affect reaction rates, and the reactions for a particular silicon species are the product of a statistical factor and rate constant. These assumptions ignore steric and inductive effects. For example, this model predicts that the relative rate constants for the four sequential hydrolysis steps leading from TMOS to Si(OH)4 would be 4 3 2 1. This model was applied to acid-catalyzed TMOS sols with W values ranging from 0.5 to 2.0. Si NMR spectra on the temporal evolution of various silicon species show the model is in excellent agreement with experimental results. A lower limit for fen was calculated as 0.2 L/mol-min. Values for few and feA are 0.006 and 0.001 L/mol-min, respectively. [Pg.642]

Due to the high reaction rates of hydrolysis and condensation reactions of metal alkoxides, information on the progressive structural evolution in transition metal systems is difficult to obtain. The 0x0 alkoxo clusters are therefore interesting models to assist in understanding the growth of three-dimensional oxide structures from the alkoxides. Some oxo-alkoxo oligomers may even be intermediates in the formation of the gel networks. [Pg.643]

Chymotrypsin secreted by the pancreas is one of the enzymes that breaks up proteins and polypeptides. Zinc plays an important role in accelerating the catalytic reaction rate. These metalloenzymes operate through activation of a carbonyl group by coordinating with its oxygen and a water molecule that acts as a nucleophile. An aCD with an appended Ni +-oxime complex at the secondary face of the aCD accelerated the reaction rate of hydrolysis of p-nitrophenyl acetate (Figure 12.5). The catalytic reaction rate is faster than that of the ocCD without appended Ni +. The reaction mechanism is reminiscent of the catalytic activity of the alkaline phosphatase enzyme. ... [Pg.222]

Biomass is resistant to chemicals at ambient temperature. Hydrolysis reactions using acid or base are very eomplex mainly because the substrate is in solid phase and the eatalyst in liquid phase. The reaction rate of hydrolysis depends on a number of variables such as temperature, acid concentration, residence time, substrate concentration and substrate composition. [Pg.331]


See other pages where Reaction rates, of hydrolysis is mentioned: [Pg.860]    [Pg.95]    [Pg.849]    [Pg.227]    [Pg.553]    [Pg.494]    [Pg.301]    [Pg.402]    [Pg.409]    [Pg.646]    [Pg.100]    [Pg.185]    [Pg.255]   
See also in sourсe #XX -- [ Pg.188 ]




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