This lesson introduces Gibbs free energy as a system property that helps predict spontaneity at constant temperature and pressure. It also explains how free energy relates to the maximum useful work a process can provide.
Here, T is the absolute temperature in kelvins, ΔH is the system’s enthalpy change, and ΔS is its entropy change. Because G is a state function, its change depends only on the initial and final states, not on the path between them.
All flashcards
Standard free-energy change from enthalpy and entropy
At a specified temperature, calculate it as ΔG∘=ΔH∘−TΔS∘.
Standard free energy of formation
The free-energy change when one mole of a substance forms from its elements in their standard states.
Free-energy changes for combined reactions
Add the reaction free-energy changes; reversing a reaction reverses the sign, and scaling it scales the change.
Nonstandard-condition free-energy change
Calculate it as ΔG=ΔG∘+RTlnQ.
Equilibrium constant and standard free energy
They are related by ΔG∘=−RTlnK.
Quiz questions
At constant temperature and pressure, what does ΔG<0 indicate for a process as written?Answer: The forward direction is thermodynamically favored.
How is ΔG∘ calculated from standard free energies of formation for a balanced reaction?Answer: Sum the stoichiometric product values and subtract the reactant sum.
For a process with ΔH<0 and ΔS>0, what does ΔG=ΔH−TΔS predict?Answer: The forward process is spontaneous at every temperature in this sign-based analysis.
For a reaction mixture with Q<K, which direction is favored as the system moves toward equilibrium?Answer: The forward direction.
If K>1 at a specified temperature, what does this indicate about the equilibrium mixture?Answer: Products are favored relative to reactants.
Based on Chemistry 2e by Paul Flowers, Klaus Theopold, Richard Langley, William R. Robinson, PhD (OpenStax), licensed CC BY 4.0. Adapted into a summary, flashcards and quizzes.