Gibbs Free Energy Calculator
Calculate the Gibbs free energy: ΔG° from an equilibrium constant, K from ΔG°, ΔG from ΔH and ΔS, and ΔG for a reaction quotient Q, at your chosen temperature.
Formula
- gas constant, 8.314462618 J/(mol·K)
- absolute temperature, in kelvin
- reaction quotient: products over reactants at the current concentrations
How it works
The Gibbs free energy change tells whether a reaction can proceed spontaneously at constant temperature and pressure: a negative ΔG favours the reaction as written. The standard value ΔG° is for all species at the standard state (1 M for solutes) and is tied to the equilibrium constant, ΔG° = −RT ln K, so a tenfold change in K changes ΔG° by about 5.7 kJ/mol at 25 °C.
Under other conditions ΔG = ΔG° + RT ln Q, and ΔG is zero when Q equals K, at equilibrium. The other route is ΔG = ΔH − TΔS, the balance of the enthalpy and entropy changes. A negative ΔG says a reaction is thermodynamically favourable; it says nothing about how fast it goes.
Worked example
An association with K = 10⁵ at 25 °C.
- T = 298.15 K, R = 8.314 J/(mol·K).
- ΔG° = −8.314 × 298.15 × ln(10⁵) = −28,540 J/mol.
ΔG° = −28.54 kJ/mol, which is −6.82 kcal/mol.
These are the values the calculator opens with, so you can check its output against this example.
Assumptions
- Constant temperature and pressure, with ideal behaviour of the solutes.
- For ΔH − TΔS, that ΔH and ΔS do not change with temperature, which fails when the heat capacity change is large.
- K for the reaction as written; reversing the reaction inverts K and changes the sign of ΔG°.
Common mistakes
- Mixing kJ and kcal (1 kcal = 4.184 kJ) or using Celsius temperatures in RT.
- Reading a negative ΔG as a fast reaction.
- Using ΔG° where the conditions are far from standard, for example a cell with different concentrations, without correcting with Q.