🔋 Gibbs Free Energy Calculator (ΔG = ΔH − TΔS)

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Enter details

Note: J, not kJ.
ΔG (kJ/mol)
-32.9576
Equilibrium constant K
594,184
Temperature (K)
298.15

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📘 About the Gibbs Free Energy

Gibbs free energy tells you whether a reaction can happen on its own at a given temperature. If ΔG = ΔH − TΔS is negative the reaction is spontaneous; if it is positive it is not; if it is zero the system is at equilibrium.

Enter the enthalpy change in kJ/mol, the entropy change in J/(mol·K) and the temperature. Using standard values (ΔH°, ΔS°) also gives the equilibrium constant from ΔG° = −RT ln K. The defaults are for the Haber process, N₂ + 3H₂ → 2NH₃.

🧮 Formula

Gibbs free energy
ΔG = ΔH − TΔS
Equilibrium constant
ΔG° = −RT ln K
Crossover temperature
T = ΔH ÷ ΔS

Where

  • ΔG = Gibbs free energy change (kJ/mol)
  • ΔH = enthalpy change (kJ/mol)
  • ΔS = entropy change (J/(mol·K); divide by 1000 for kJ)
  • T = absolute temperature (K)
  • R = 8.314 J/(mol·K)
Spontaneous means thermodynamically possible, not fast. Diamond turning into graphite is spontaneous but takes millions of years.

✏️ Worked examples

Haber process at 25 °C

You enter
Enthalpy change (ΔH)-92.2 kJ/mol
Entropy change (ΔS)-198.7 J/(mol·K)
Temperature (T)25 °C
You get
ΔG (kJ/mol)-32.9576
Equilibrium constant K594,184
Temperature (K)298.15

ΔG = -32.9576 kJ/mol, so making ammonia is spontaneous at room temperature.

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Haber process at 500 °C

You enter
Enthalpy change (ΔH)-92.2 kJ/mol
Entropy change (ΔS)-198.7 J/(mol·K)
Temperature (T)500 °C
You get
ΔG (kJ/mol)61.4249
Equilibrium constant K7.08214e-5
Temperature (K)773.15

At 500 °C, ΔG = 61.4249 kJ/mol: the reaction is no longer spontaneous, which is why a balance of temperature and pressure is used.

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🧭 How to use this calculator

What you enter

  • Enthalpy change (ΔH) (kJ/mol)
  • Entropy change (ΔS) (J/(mol·K))Note: J, not kJ.
  • Temperature (T) (°C)

What you get

  • ΔG (kJ/mol)
  • Equilibrium constant K
  • Temperature (K)

💡 Effect of ΔH and ΔS on spontaneity

  • ΔH negative, ΔS positive: spontaneous at all temperatures.
  • ΔH positive, ΔS negative: never spontaneous.
  • ΔH negative, ΔS negative: spontaneous at low temperatures (below ΔH/ΔS).
  • ΔH positive, ΔS positive: spontaneous at high temperatures (above ΔH/ΔS).

❓ Frequently asked questions

What is the formula for Gibbs free energy?

ΔG = ΔH − TΔS.

When is a reaction spontaneous?

When ΔG is negative.

Why divide ΔS by 1000?

ΔH is usually in kJ/mol and ΔS in J/(mol·K), so ΔS must be converted to kJ to match.

How is ΔG related to the equilibrium constant?

ΔG° = −RT ln K. A negative ΔG° gives K > 1, favouring products.