Gibbs Free Energy of Reaction (ΔG°rxn) Calculator for 2H₂S


Gibbs Free Energy of Reaction (ΔG°rxn) Calculator for 2H₂S

Determine the spontaneity of the hydrogen sulfide decomposition reaction.

Reaction Calculator

Reaction: 2H₂S(g) ⇌ 2H₂(g) + S₂(g)


Standard Gibbs free energy of formation for hydrogen sulfide in kJ/mol.


Standard Gibbs free energy of formation for hydrogen gas in kJ/mol. (0 for elements in standard state)


Standard Gibbs free energy of formation for diatomic sulfur in kJ/mol.


The temperature at which the reaction occurs.



What is the Gibbs Free Energy of Reaction (ΔG°rxn)?

The Gibbs Free Energy of Reaction (often denoted as ΔG°rxn) is a thermodynamic potential that measures the maximum reversible work that may be performed by a thermodynamic system at a constant temperature and pressure. In simpler terms, it tells us whether a chemical reaction will occur spontaneously. For a reaction to be spontaneous, the change in Gibbs free energy must be negative (ΔG < 0). If ΔG is positive, the reaction is non-spontaneous and requires energy input to proceed. If ΔG is zero, the system is at equilibrium. This calculator specifically helps you calculate the Gibbs Free Energy of Reaction for 2H₂S.

Gibbs Free Energy of Reaction for 2H₂S Formula and Explanation

The calculation for the standard Gibbs free energy of reaction (ΔG°rxn) uses the “products minus reactants” rule, summing the standard Gibbs free energies of formation (ΔG°f) for each component, multiplied by their stoichiometric coefficients (the numbers in front of them in the balanced equation).

The general formula is:

ΔG°rxn = ΣnΔG°f(products) – ΣmΔG°f(reactants)

For the specific reaction 2H₂S(g) ⇌ 2H₂(g) + S₂(g), the formula becomes:

ΔG°rxn = [ (2 × ΔG°f of H₂) + (1 × ΔG°f of S₂) ] – [ 2 × ΔG°f of H₂S ]

Variables in the Gibbs Free Energy Calculation
Variable Meaning Unit (Auto-inferred) Typical Range
ΔG°rxn Standard Gibbs Free Energy of Reaction kJ/mol -1000 to 1000
ΔG°f Standard Gibbs Free Energy of Formation kJ/mol -1600 to 300
n, m Stoichiometric Coefficients Unitless 1, 2, 3…
T Temperature K or °C -273 to 1000+

Practical Examples

Example 1: Standard Conditions

Let’s calculate the Gibbs Free Energy of Reaction for 2H₂S under standard conditions (25°C or 298.15 K) using typical ΔG°f values.

  • Inputs:
    • ΔG°f of H₂S = -33.4 kJ/mol
    • ΔG°f of H₂ = 0 kJ/mol
    • ΔG°f of S₂ = 79.7 kJ/mol
    • Temperature = 25 °C
  • Calculation:
    • Products Energy = [2 * 0] + [1 * 79.7] = 79.7 kJ/mol
    • Reactants Energy = [2 * -33.4] = -66.8 kJ/mol
    • ΔG°rxn = 79.7 – (-66.8) = 146.5 kJ/mol
  • Result: A ΔG°rxn of +146.5 kJ/mol indicates the reaction is non-spontaneous under these conditions.

Example 2: Hypothetical High Temperature

Gibbs free energy is dependent on temperature. Although this specific calculator uses ΔG°f values which are defined at a standard temperature, the general equation ΔG = ΔH – TΔS shows this dependency. A full analysis would require enthalpy (ΔH) and entropy (ΔS) values. However, this calculator focuses on the standard-state calculation, which is a foundational concept. To explore temperature’s impact further, you might consult a entropy calculator.

How to Use This Gibbs Free Energy of Reaction for 2H₂S Calculator

  1. Enter ΔG°f for Reactants: Input the known standard Gibbs free energy of formation for H₂S. The standard value is pre-filled.
  2. Enter ΔG°f for Products: Input the values for H₂ and S₂. Note that the value for elements in their standard state, like H₂, is 0.
  3. Set Temperature: Enter the temperature and select the correct unit (°C or K). While ΔG°f values are standard at 298.15 K, the calculator shows the selected temperature for context.
  4. Calculate: Click the “Calculate ΔG°rxn” button.
  5. Interpret Results: The calculator will display the final ΔG°rxn, along with intermediate energy totals for the products and reactants. A negative result means the reaction is spontaneous. A positive result means it is non-spontaneous. You can also consult a thermodynamics calculator for more advanced problems.

Key Factors That Affect Gibbs Free Energy of Reaction for 2H₂S

  • Temperature: As shown in the Gibbs free energy equation (ΔG = ΔH – TΔS), temperature (T) directly influences the spontaneity of a reaction.
  • Pressure: Changes in pressure can affect the Gibbs free energy, especially for reactions involving gases, by altering the entropy of the system.
  • Concentration: The Gibbs free energy change depends on the concentrations of reactants and products, as described by the relationship involving the reaction quotient (Q).
  • Standard State: The reference point for calculations (ΔG°) is the standard state (usually 298.15 K and 1 bar pressure), but real-world conditions vary.
  • Enthalpy (ΔH): Whether a reaction is exothermic (releases heat, negative ΔH) or endothermic (absorbs heat, positive ΔH) is a major component of the final ΔG value.
  • Entropy (ΔS): The change in the system’s disorder or randomness (ΔS) is the other key component. An increase in entropy (positive ΔS) favors spontaneity. For details, see an enthalpy-entropy interaction guide.

Frequently Asked Questions (FAQ)

What does a negative ΔG°rxn mean?

A negative ΔG°rxn indicates that a reaction is spontaneous under standard conditions, meaning it can proceed without external energy input.

What does a positive ΔG°rxn mean?

A positive ΔG°rxn means the reaction is non-spontaneous. It will not happen on its own and requires a continuous input of energy to proceed.

Why is the ΔG°f for H₂(g) zero?

The standard Gibbs free energy of formation for any element in its most stable form (its standard state) is defined as zero. This provides a baseline for calculations.

What unit is Gibbs Free Energy measured in?

Gibbs Free Energy is typically measured in kilojoules per mole (kJ/mol).

How does temperature affect the spontaneity of this reaction?

The effect of temperature depends on the signs of the enthalpy change (ΔH) and entropy change (ΔS). The term -TΔS in the equation ΔG = ΔH – TΔS shows that as temperature (T) increases, the entropy contribution becomes more significant.

Can a reaction with a positive ΔG°rxn still happen?

Yes. A positive ΔG°rxn refers to standard conditions. Under non-standard conditions (different pressures or concentrations), the actual ΔG can be negative. Also, a non-spontaneous reaction can be driven by coupling it with a highly spontaneous reaction.

What is the difference between ΔG and ΔG°?

ΔG° refers to the standard-state free energy change (fixed concentrations, pressures). ΔG is the free energy change under any set of non-standard conditions and is more indicative of spontaneity in real-world scenarios.

Does a spontaneous reaction happen quickly?

Not necessarily. Spontaneity (thermodynamics) is different from reaction rate (kinetics). A spontaneous reaction can be incredibly slow if it has a high activation energy. A reaction kinetics calculator could provide more insight here.

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