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Equilibrium constant range

The binding between the substrate and the enzyme is often provided by relatively weak hydrogen bonds. The E-S complexes have equilibrium constants ranging from one hundredth to one hundred millionth M, which corresponds to interaction free energies of -3 to -12 kcal/mol much lower than the value of -450 kJ/mol characteristic for a covalent bond. [Pg.329]

At temperatures of 220 C and higher, l-fluoro-2-methylenecyclopropane (8) and (fluoromethyl-enejcyclopropane (9) were smoothly interconverted with an equilibrium constant ranging from 5.82 (289.6 °C) to 7.70 (229.0 °C). A similar observation was made with the analogous geminal difluoro compounds. ... [Pg.2300]

As shown In Figure 9, for orders of magnitude change In the carrier concentration and membrane thickness, they found that their dimensionless equilibrium constant ranged only between 1 and 10. Their result provides a useful method to screen potential carriers and also to determine the comparison between actual and optimum performance. Noble (61) recently defined a kinetic efficiency factor. [Pg.14]

Equilibrium constants range over many orders of magnitude. Values as small as 10 are known, as are values as high as 10 or greater. What does the size of the equilibrium constant tell us about the reaction If we look at the equilibrium expression for a reaction as an algebraic relationship, the answer will become apparent. [Pg.488]

Alkylammes differ very little among themselves m basicity Their basicities cover a range of less than 10m equilibrium constant (1 pkf unit)... [Pg.919]

Molecular absorption, particularly in the UV/Vis range, has been used for a variety of different characterization studies, including determining the stoichiometry of metal-ligand complexes and determining equilibrium constants. Both of these examples are examined in this section. [Pg.403]

Thermodynamically, the formation of methane is favored at low temperatures. The equilibrium constant is 10 at 300 K and is 10 ° at 1000 K (113). High temperatures and catalysts ate needed to achieve appreciable rates of carbon gasification, however. This reaction was studied in the range 820—1020 K, and it was found that nickel catalysts speed the reaction by three to four orders of magnitude (114). The Hterature for the carbon-hydrogen reaction has been surveyed (115). [Pg.417]

These considerations apart, die selection of die optimum conditions for die performance of a transporting reaction requires die choice of die best average value of die equilibrium constant. The effect of die range in die... [Pg.86]

Taking known values for the molar refractivities of water and methanol, and again assuming a range of values for the equilibrium constant (k) and the refractive index (ni) of the methanol/water associate, the actual values that fit the equation for these... [Pg.130]

It is seen that the three values for the equilibrium constant (k) range from 0.00443 to 0.00565 with an average value of 0.00504. The two values for the densities of the methanol/water associate are in reasonable agreement and have a magnitude that would be expected for the hydrogen bonded associate. [Pg.131]

Using the average value for the equilibrium constant, the distribution concentration of the different components of a methanol water mixture were calculated for initial methanol concentrations ranging from zero to 100%v/v. The curves they obtained are shown in Figure 28. The molar refractivities of 11.88 is also in accordance with that expected since the molar refractivity s of water and methanol are 3.72 and 8.28 respectively. The refractive index of the associate of 1.3502 is, as would be expected, higher than that of either water or methanol. [Pg.131]

PK. — the negative logarithm of the equilibrium constant for acids or bases. This parameter is an indicator of the strength of an acid or base. Strong acids, such as H2SO4, and HCl, have low pK s (i.e., -1.0) while strong bases such as KOH and NaOH, have pK s close to 14.0. Weak acids and weak bases fall in the intermediate range. [Pg.162]

Both the principles of chemical reaction kinetics and thermodynamic equilibrium are considered in choosing process conditions. Any complete rate equation for a reversible reaction involves the equilibrium constant, but quite often, complete rate equations are not readily available to the engineer. Thus, the engineer first must determine the temperature range in which the chemical reaction will proceed at a... [Pg.59]

John F. Brandts measured the equilibrium constants for the denaturation over a range of pH and temperatures. The data for pH 3 ... [Pg.59]

Values obtained in this way for various proton transfers, over a wide range of temperature, are given in Table 9. In some cases equilibrium constants have been accurately determined by measurements of the elec-... [Pg.120]

Now look at the numerical values of the equilibrium constants. The K s listed range from 10+1 to 10 16, so we see there is a wide variation. We want to acquire a sense of the relation between the size of the equilibrium constant and the state of equilibrium. A large value of K must mean that at equilibrium there are much larger concentrations present of products than of reactants. Remember that the numerator of our equilibrium expression contains the concentrations of the products of the reaction. The value of 2 X 10,s for the K for reaction (19) certainly indicates that if a reaction is initiated by placing metallic copper in a solution containing Ag+ (for example, in silver nitrate solution), when equilibrium is finally reached, the concentration of Cu+2 ion, [Cu+2], is very much greater than the square of the silver ion concentration, [Ag+]2. [Pg.154]

In the lead-acid battery, sulfuric acid has to be considered as an additional component of the charge-discharge reactions. Its equilibrium constant influences the solubility of Pb2+ and so the potential of the positive and negative electrodes. Furthermore, basic sulfates exist as intermediate products in the pH range where Fig. 1 shows only PbO (cf. corresponding Pour-baix diagrams in Ref. [5], p. 37, or in Ref. [11] the latter is cited in Ref. [8]). Table 2 shows the various compounds. [Pg.159]

In the region of pure CH4, the equilibrium is governed by Equation 4. For this reaction, the equilibrium constant increases with temperature so that at high enough temperatures there will be appreciable dissociation of CH4 to H2 and graphite. In the lower temperature range considered here, the thermodynamic equilibrium indicates only a very small amount of dissociation so the intersection of the graphite deposition curve with the H2-CH4 line occurs at almost pure CH4. As the temperature increases, the point of intersection will move toward pure H2 on the H2-CH4 line. [Pg.47]

A wide range of nitroxidcs and derived alkoxyamincs has now been explored for application in NMP. Experimental work and theoretical studies have been carried out to establish structure-property correlations and provide further understanding of the kinetics and mechanism. Important parameters are the value of the activation-deactivation equilibrium constant K and the values of kaa and (Scheme 9.17), the combination disproportionation ratio for the reaction of the nilroxide with Ihe propagating radical (Section 9.3.6.3) and the intrinsic stability of the nitroxide and the alkoxyamine under the polymerization conditions (Section 9.3.6.4). The values of K, k3Cl and ktieact are influenced by several factors.11-1 "7-"9 ... [Pg.472]


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See also in sourсe #XX -- [ Pg.542 , Pg.543 ]

See also in sourсe #XX -- [ Pg.542 , Pg.543 ]

See also in sourсe #XX -- [ Pg.544 , Pg.545 ]




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