Book: KE & R: 20 Flashcards
Quantifying entropy in terms of the number of microstates (W) over which the energy of a system can be dispersed.
S = k ln W
Quantifying the entropy change in terms of heat absorbed (or released) in a reversible process.
∆S_sys = q_rev / T
Stating the second law of thermodynamics for a spontaneous process.
∆S_univ = ∆S_sys + ∆S_surr > 0
Calculating the standard entropy of reaction from the standard molar entropies of reactants and products.
∆Sº_rxn = m Σ Sº_products - n Σ Sº_reactants
Relating the entropy change in the surroundings to the enthalpy change of the system and the temperature.
∆S_surr = - ∆H_sys / T
Expressing the free energy change of the system in terms of its component enthalpy and entropy changes (Gibbs equation).
∆G_sys = ∆H_sys - T ∆S_sys
Calculating the standard free energy change from standard enthalpy and entropy changes.
∆Gº_sys = ∆Hº_sys - T ∆Sº_sys
Calculating the standard free energy change from the standard free energies of formation.
∆Gº_rxn = m Σ Gº_(f)products - n Σ Gº_(f)reactants
Relating the free energy change to the maximum work a system can do.
∆G = w_max
Finding the temperature at which a reaction becomes spontaneous.
T = ∆H / ∆S
Expressing the free energy change in terms of Q and K.
∆G = RT ln( Q / K ) = RT (ln Q - ln K)
Expressing the free energy change with Q and at standard-state conditions.
∆Gº = - RT ln K
Expressing the free energy change for nonstandard initial conditions.
∆G = ∆Gº + RT ln Q