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A mixture of cis-decalin and CXB can simultaneously match optical index and density of PMMA. [1] Due to the moderate dielectric constant of CXB (ε = 7.9 [ 2 ] ), PMMA acquires charges that can be screened by the addition of salt (e.g. tetrabutyl ammonium bromide ), leading to a very good approximation of colloidal hard sphere . [ 3 ]
[1] The change in the extent of reaction is then defined as [2] [3] = where denotes the number of moles of the reactant or product and is the stoichiometric number [4] of the reactant or product. Although less common, we see from this expression that since the stoichiometric number can either be considered to be dimensionless or to have units ...
The sulfur radical was found to be more reactive (6*10 8 vs. 1*10 7 M −1.s −1) and less selective (selectivity ratio 76 vs 1200) than the carbon radical. In this case, the effect can be explained by extending the Bell–Evans–Polanyi principle with a factor δ {\displaystyle \delta \,} accounting for transfer of charge from the reactants ...
where A and B are reactants C is a product a, b, and c are stoichiometric coefficients,. the reaction rate is often found to have the form: = [] [] Here is the reaction rate constant that depends on temperature, and [A] and [B] are the molar concentrations of substances A and B in moles per unit volume of solution, assuming the reaction is taking place throughout the volume of the ...
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 ...
When the enyne moiety is incorporated into a 10-membered hydrocarbon ring (e.g. cyclodeca-3-ene-1,5-diyne in scheme 2) the reaction, taking advantage of increased ring strain in the reactant, is possible at the much lower temperature of 37 °C. Scheme 2. Bergman reaction of cyclodeca-3-ene-1,5-diyne
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 ]
Living cationic polymerization is a living polymerization technique involving cationic propagating species. [1] [2] It enables the synthesis of very well defined polymers (low molar mass distribution) and of polymers with unusual architecture such as star polymers and block copolymers and living cationic polymerization is therefore as such of commercial and academic interest.