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Gibbs free energy changes, determination

It is known that thermodynamic and structural studies are mutually complimentary and both are necessary for a complete elucidation of the molecular details of any binding process for the delineation of the molecular interaction involved at the interaction site. The Gibbs free energy change (AG) may be determined from the binding constant from the relation ... [Pg.172]

As equation 2.4.8 indicates, the equilibrium constant for a reaction is determined by the temperature and the standard Gibbs free energy change (AG°) for the process. The latter quantity in turn depends on temperature, the definitions of the standard states of the various components, and the stoichiometric coefficients of these species. Consequently, in assigning a numerical value to an equilibrium constant, one must be careful to specify the three parameters mentioned above in order to give meaning to this value. Once one has thus specified the point of reference, this value may be used to calculate the equilibrium composition of the mixture in the manner described in Sections 2.6 to 2.9. [Pg.10]

AG° is the standard Gibbs free energy change of reaction obtained from the standard energy of formation of pure components AG at 25 °C, P = 1 atm and a suitable aggregation state. Once having determined IQq in standard conditions, the van t Hoff equation may be used to calculate fQq at other temperatures, as follows ... [Pg.471]

Calculate AG° and Kfor each independent reaction. This may be done as in the relevant examples earlier in this section, with determination of AG° as a function of temperature. An easier route, however, is to use the standard Gibbs free-energy change of formation A Gy for each compound at the temperature of interest in the relationship... [Pg.135]

The normal isotopic abundances for Li are 92.48 mole % for 7Li and 7.52 mole % for 6Li. Making reasonable approximations, determine the entropy, enthalpy, and Gibbs free energy changes on mixing the pure isotopes. Discuss your results in terms of the statements made in Section 1.21 in conjunction with the Third Law of Thermodynamics. [Pg.355]

Devise strategies for determining enthalpy changes and Gibbs free energy changes at pressures different from 1 bar. [Pg.197]

Yet another approach to the determination of AG is apparent when considering another definition of the standard Gibbs free-energy change as the difference between the energies of formation of products and reactants ... [Pg.17]

The solubility product constant may be determined by direct measnrements or calcnlated from the standard Gibbs free energies of formation (JsGf) of the species involved at their standard states. For the reaction scheme (Equation 8.13) the Gibbs free energy change is ... [Pg.447]

Entropy and Entropy is a measure of molecular disorder. Entropy changes (AS) can be combined with AH free energy in the Gibbs free energy change (AG), which determines the overall thermodynamic... [Pg.43]

Gibbs free-energy change (p. 126) intermediate (p. 136) kinetics (p. 131) kinetic stability (p. 131) mechanism of the reaction (p. 123) nucleophile (p. 122) rate constant (p. 132) rate-determining step (p. 136)... [Pg.138]

We have thus expressed the quantity fi in terms of the Gibbs free energy change for formation of a cluster of size i at saturation (S 1). Now we need to determine AG,. [Pg.497]


See other pages where Gibbs free energy changes, determination is mentioned: [Pg.1290]    [Pg.1290]    [Pg.60]    [Pg.253]    [Pg.97]    [Pg.278]    [Pg.540]    [Pg.366]    [Pg.193]    [Pg.268]    [Pg.511]    [Pg.190]    [Pg.331]    [Pg.96]    [Pg.9]    [Pg.17]    [Pg.43]    [Pg.126]    [Pg.268]    [Pg.58]    [Pg.239]    [Pg.28]    [Pg.292]    [Pg.149]    [Pg.198]    [Pg.443]    [Pg.349]    [Pg.40]    [Pg.396]    [Pg.40]    [Pg.71]    [Pg.85]    [Pg.90]    [Pg.526]    [Pg.742]    [Pg.151]    [Pg.281]   
See also in sourсe #XX -- [ Pg.68 ]




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