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17.8: Calculating Standard Free Energy Changes

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Calculating Standard Free Energy Changes

17.8: Calculating Standard Free Energy Changes

The free energy change for a reaction that occurs under the standard conditions of 1 bar pressure and at 298 K is called the standard free energy change. Since free energy is a state function, its value depends only on the conditions of the initial and final states of the system. A convenient and common approach to the calculation of free energy changes for physical and chemical reactions is by use of widely available compilations of standard state thermodynamic data. One method involves the use of standard enthalpies and entropies to compute standard free energy changes, ΔG°, according to the following relation.


The standard free energy change for a reaction may also be calculated from the standard free energy of formation ΔGf° values of the reactants and products involved in the reaction. The standard free energy of formation is the free energy change that accompanies the formation of one mole of a substance from its elements in their standard states. Similar to the standard enthalpy of formation, ΔGf° is by definition zero for elemental substances under standard state conditions. For the reaction


the standard free energy change at room temperature may be calculated as


The use of free energies of formation to compute free energy changes for reactions as described above is possible because ΔG is a state function, and the approach is analogous to the use of Hess’ Law in computing enthalpy changes. Consider the vaporization of water as an example:


An equation representing this process may be derived by adding the formation reactions for the two phases of water (necessarily reversing the reaction for the liquid phase). The free energy change for the sum reaction is the sum of free energy changes for the two added reactions:


This approach may also be used in cases where a nonspontaneous reaction is enabled by coupling it to a spontaneous reaction. For example, the production of elemental zinc from zinc sulfide is thermodynamically unfavorable, as indicated by a positive value for ΔG°1:


The industrial process for the production of zinc from sulfidic ores involves coupling this decomposition reaction to the thermodynamically favorable oxidation of sulfur:


The coupled reaction exhibits a negative free energy change and is spontaneous:


This process is typically carried out at elevated temperatures, so this result obtained using standard free energy values is just an estimate. The gist of the calculation, however, holds true.

This text is adapted from Openstax, Chemistry 2e, Chapter 16.4: Free Energy.


Standard Free Energy Change Chemical Reaction Standard Condition Standard ∆G Formation Calcium Carbonate Calcium Oxide Carbon Dioxide Standard Enthalpy Change Standard Entropy Change Reference Tables Standard Molar Entropies 298 K J Difference Products Reactants Stoichiometric Coefficients Hydrogen Gas Chlorine Gas Hydrogen Chloride Gas

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