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Gibbs Energy of an Ideal Gas

General Chemistry • Spontaneous Change Entropy and Gibbs Energy

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Gibbs Energy of an Ideal Gas (Isothermal, Pressure Change)

For an ideal gas undergoing an isothermal change in pressure from \(P^{\circ}\) to \(P\), the Gibbs energy change and the (molar) Gibbs energy are

\[ \begin{aligned} \Delta G \;&=\; nRT \,\ln\!\left(\frac{P}{P^{\circ}}\right) \\[2pt] G \;&=\; G^{\circ} + nRT \,\ln\!\left(\frac{P}{P^{\circ}}\right) \\[2pt] G_m \;&=\; G_m^{\circ} + RT \,\ln\!\left(\frac{P}{P^{\circ}}\right) \end{aligned} \]
mol

Use consistent units: the calculator converts pressures to the same base before taking the ratio \(P/P^{\circ}\). \(R = 8.314\,462\,618\ \mathrm{J\,mol^{-1}\,K^{-1}}\).

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Enter \(n, T, P, P^{\circ}\) (and \(G^{\circ}\) or \(G_m^{\circ}\) if needed), then choose what to solve for.

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Frequently Asked Questions

What is the formula for Gibbs energy change of an ideal gas when pressure changes?

For an isothermal change, the calculator uses Delta G = n x R x T x ln(P2/P1). This comes from how the chemical potential of an ideal gas depends on pressure.

Why does the pressure unit not matter in ln(P2/P1)?

Because P2/P1 is a ratio, the units cancel as long as both pressures are expressed in the same unit. The logarithm must take a dimensionless quantity.

When is Delta G negative for a pressure change of an ideal gas?

Delta G is negative when P2 < P1 because ln(P2/P1) is negative. This corresponds to a decrease in pressure at constant temperature, such as expansion to a lower pressure.

Can I use this calculator if temperature changes during the process?

This relation applies to isothermal changes. If temperature changes, the Gibbs energy change must be evaluated with a path that accounts for the temperature dependence.