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- https://chem.libretexts.org/Courses/Williams_School/Chemistry_I/08%3A_State_Changes_and_Thermodynamics/8.10%3A_Gibbs_EnergyGibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates that the reaction wil...Gibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates that the reaction will proceed in the forward direction to reach equilibrium; a positive ΔG indicates that the reaction will proceed in the reverse direction to reach equilibrium; and a ΔG of zero indicates that the system is at equilibrium. A number of approaches to the computation of free energy changes are possible.
- https://chem.libretexts.org/Workbench/OpenStax_Chemistry_Remixed%3A_Clovis_Community_College/16%3A_Thermodynamics/16.05%3A_Free_EnergyGibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates that the reaction wil...Gibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates that the reaction will proceed in the forward direction to reach equilibrium; a positive ΔG indicates that the reaction will proceed in the reverse direction to reach equilibrium; and a ΔG of zero indicates that the system is at equilibrium. A number of approaches to the computation of free energy changes are possible.
- https://chem.libretexts.org/Courses/SUNY_Oneonta/Chem_221%3A_Organic_Chemistry_I_(Bennett)/3%3AStuff_to_Review_from_General_Chemistry/10%3A_Thermodynamics/10.04%3A_Gibbs_EnergyGibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates a spontaneous process...Gibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates a spontaneous process; a positive ΔG indicates a nonspontaneous process; and a ΔG of zero indicates that the system is at equilibrium. A number of approaches to the computation of free energy changes are possible.
- https://chem.libretexts.org/Courses/Thompson_Rivers_University/TRU%3A_Fundamentals_and_Principles_of_Chemistry_(CHEM_1510_and_CHEM_1520)/08%3A_Entropy_and_Free_Energy/8.04%3A_Gibbs_Free_EnergyGibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates that the reaction wil...Gibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates that the reaction will proceed in the forward direction to reach equilibrium; a positive ΔG indicates that the reaction will proceed in the reverse direction to reach equilibrium; and a ΔG of zero indicates that the system is at equilibrium. A number of approaches to the computation of free energy changes are possible.
- https://chem.libretexts.org/Bookshelves/General_Chemistry/Chemistry_1e_(OpenSTAX)/16%3A_Thermodynamics/16.04%3A_Gibbs_EnergyGibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates that the reaction wil...Gibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates that the reaction will proceed in the forward direction to reach equilibrium; a positive ΔG indicates that the reaction will proceed in the reverse direction to reach equilibrium; and a ΔG of zero indicates that the system is at equilibrium. A number of approaches to the computation of free energy changes are possible.
- https://chem.libretexts.org/Courses/City_College_of_San_Francisco/Chemistry_101B/05%3A_Thermodynamics/5.4%3A_Gibbs_EnergyGibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates a spontaneous process...Gibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates a spontaneous process; a positive ΔG indicates a nonspontaneous process; and a ΔG of zero indicates that the system is at equilibrium. A number of approaches to the computation of free energy changes are possible.
- https://chem.libretexts.org/Courses/Widener_University/CHEM_176%3A_General_Chemistry_II_(Fischer-Drowos)/08%3A_Thermodynamics/8.06%3A_Free_EnergyGibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates that the reaction wil...Gibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates that the reaction will proceed in the forward direction to reach equilibrium; a positive ΔG indicates that the reaction will proceed in the reverse direction to reach equilibrium; and a ΔG of zero indicates that the system is at equilibrium. A number of approaches to the computation of free energy changes are possible.
- https://chem.libretexts.org/Courses/Westminster_College/CHE_180_-_Inorganic_Chemistry/06%3A_Chapter_6_-_Inorganic_Thermodynamics/6.4%3A_Gibbs_EnergyGibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates a spontaneous process...Gibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates a spontaneous process; a positive ΔG indicates a nonspontaneous process; and a ΔG of zero indicates that the system is at equilibrium. A number of approaches to the computation of free energy changes are possible.
- https://chem.libretexts.org/Courses/Valley_City_State_University/Chem_122/Chapter_5%3A_Chemical_Equilibrium/5.7%3A_Gibbs_EnergyGibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates a spontaneous process...Gibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates a spontaneous process; a positive ΔG indicates a nonspontaneous process; and a ΔG of zero indicates that the system is at equilibrium. A number of approaches to the computation of free energy changes are possible.
- https://chem.libretexts.org/Courses/Nassau_Community_College/General_Chemistry_II/06%3A_Thermodynamics/6.04%3A_Gibbs_EnergyGibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates a spontaneous process...Gibbs free energy (G) is a state function defined with regard to system quantities only and may be used to predict the spontaneity of a process. A negative value for ΔG indicates a spontaneous process; a positive ΔG indicates a nonspontaneous process; and a ΔG of zero indicates that the system is at equilibrium. A number of approaches to the computation of free energy changes are possible.
- https://chem.libretexts.org/Bookshelves/General_Chemistry/ChemPRIME_(Moore_et_al.)/16%3A_Entropy_and_Spontaneous_Reactions/16.14%3A_The_Free_EnergyIf we assume, as we did previously, that neither ΔH m ° nor ΔS m ° varies much as the temperature changes from 298 K to the temperature in question, we can then use the values of ΔH m °(298 K) obtaine...If we assume, as we did previously, that neither ΔH m ° nor ΔS m ° varies much as the temperature changes from 298 K to the temperature in question, we can then use the values of ΔH m °(298 K) obtained from the Table of Some Standard Enthalpies of Formation at 25°C and ΔS m °(298 K) obtained from the Table of Standard Molar Entropies to calculate ΔG m ° for the temperature in question.
