Gibbs Free Energy Calculations (College Board AP® Chemistry): Revision Note
Gibbs Free Energy, Enthalpy & Entropy
Enthalpy change (ΔH°) and entropy change (ΔS°) come together in a fundamental thermodynamic concept called the Gibbs free energy (G)
The Gibbs free-energy equation is:
ΔG° = ΔH° − TΔS°
The units of ΔG° are in kJ mol-1
The units of ΔH° are in kJ mol-1
The units of T are in K
The units of ΔS° are in J K-1 mol-1 (and must therefore be converted to kJ K-1 mol-1 by dividing by 1000)
When ΔG° is negative, the reaction is thermodynamically favored and likely to occur
When ΔG° is positive, the reaction is not thermodynamically favored and unlikely to occur
Worked Example
Calculate ΔG° for the following reaction at 298 K.
2NaHCO3 (s) → Na2CO3 (s) + H2O (l) + CO2 (g)
ΔH° = +135 kJ mol-1
ΔS° = +344 J K-1 mol-1
Answer:
Step 1: Convert the entropy value to kilojoules
ΔS°= +344 J K-1 mol-1 ÷ 1000 = +0.344 kJ K-1 mol-1
Step 2: Substitute the terms into the Gibbs Equation
ΔG° = ΔH°− TΔS°
ΔG° = +135 − (298 × 0.344)
ΔG° = +32.49 kJ mol-1
So, the reaction is thermodynamically unfavorable at 298 K
Worked Example
Determine whether the following reaction is thermodynamically favored at 298 K.
2Ca (s) + O2 (g) → 2CaO (s) ΔH = −635.5 kJ mol-1
S° [Ca (s)] = 41.00 J K-1 mol-1
S° [O2 (g)] = 205.0 J K-1 mol-1
S° [CaO (s)] = 40.00 J K-1 mol-1
Answer:
Step 1: Calculate ΔS°
ΔS° = ΣΔS° products − ΣΔS° reactants
ΔS° = (2 × ΔS° [CaO (s)]) − (2 × ΔS° [Ca (s)] + ΔS° [O2 (g)])
ΔS° = (2 × 40.00) − (2 × 41.00 + 205.0)
ΔS° = −207.0 J K-1 mol-1
Step 2: Convert ΔS° to kJ K-1 mol-1
ΔS° = −207.0 J K-1 mol-1 ÷ 1000 = −0.207 kJ mol-1
Step 3: Calculate ΔG°
ΔG°= ΔH° − TΔS°
ΔG° = −635.5 − (298 × −0.207)
ΔG°= −573.8 kJ mol-1
Since ΔG° is negative, the reaction is thermodynamically favored
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