1.4.2 (HL)—Gibbs energy (ΔG)
- Syllabus
- First assessment 2025
- Objective
- 1.4.2
- Level
- HL
ΔG°=ΔH°−TΔS°
Use an absolute temperature in kelvin and convert ΔS° to the same energy units as ΔH° before subtracting TΔS°. The result is the Gibbs energy change for the stated reaction.
Under the stated standard conditions, ΔG° < 0 is thermodynamically favourable, ΔG° = 0 marks equilibrium, and ΔG° > 0 favours the reverse direction. This criterion predicts feasibility, not how fast the change occurs.
Worked Gibbs example: for propane combustion to gaseous water, the local course book gives ΔH∘=−2045kJmol−1 and ΔS∘=+103JK−1mol−1 at 5∘C. Convert T=278.15K and ΔS∘=0.103kJK−1mol−1; then ΔG∘=−2045−(278.15)(0.103)=−2074kJmol−1. Its negative sign means the stated reaction is spontaneous under those standard conditions, not necessarily fast.
Representative question
Calculate the Gibbs energy change, ΔGθ in kJmol−1, for this reaction under standard conditions. Use the value of −4 kJ mol−1 for ΔHθr and your answer from (d)(iv). If you did not obtain an answer for (d)(iv) use −10JK−1 mol−1, although this is not the correct answer. Use sections 1 and 4 of the data booklet.
conversion to common units
⟨ΔGθ=−4 kJ mol−1−298 K−0.008 kJ K−1 mol−1»−6.4« kJ mol−1» ↓
M1 is for conversion to common units M2 is for correct value.
Award [2] for correct final answer. If −10 J K−1 mol−1 is used, the answer will be -1.0 « kJmol−1 ».
Retrieve the route: identify complete or incomplete combustion products, compare fuels and biofuels, balance fuel-cell half-equations, calculate ΔS° and ΔG°, then use ΔG, Q and K to reason about spontaneity and equilibrium.
Check products before balancing, evidence before evaluation, oxidation versus reduction, kelvin and unit consistency, the sign of ΔG, and whether Q is below, equal to, or above K.