Why is DeltaG Negative for H2O(l) to H2O(g) at Equilibrium?

In summary, the equilibrium vapor pressure of water at 100°C is 1 bar. This means that at equilibrium, the partial pressure of water would be 1 atm. However, the reaction is reversible and continuously occurring, with vapor molecules condensing into the liquid phase and liquid molecules evaporating into the gas phase. When P(H2O) is less than 1 atm, the rate of evaporation exceeds the rate of condensation, and when P(H2O) is greater than 1 atm, the opposite occurs. Only when P(H2O) = 1 atm will there be no net exchange of material between the liquid and gaseous phases. Therefore, it is incorrect to use an "=" sign between the reactants
  • #1
Kqwert
160
3
Please post this type of questions in HW section using the template.
Calculate deltaG for the reaction:

H2O(l) = H2O(g). 100 degrees celsius, water is clean. P(H2O) = 0.1 bar.

Given that it is an equilibrium, I'd think that deltaG would be zero. But the answer is in fact negative. How is that possible?
 
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  • #2
What is the equilibrium vapor pressure of water at 100°C?
 
  • #3
1 bar? So it's really not an equilibrium..?
 
  • #4
At equilibrium, the partial pressure of water would be 1 atm. Because P(H2O) is less than that, the forward reaction is favored.
 
  • #5
So it's wrong to call it an equilibrium?
 
  • #6
The reaction is at equilibrium only at a specific P(H2O).
 
  • #7
Thank you!
isn't it wrong to write the equation with a "=" sign between the reactants and products then?
 
  • #8
H2O(g) ##\rightleftharpoons## H2O(l) is the correct notation.

The reaction is reversible, with vapor molecules continuously condensing into the liquid phase and liquid molecules continuously evaporating into the gas phase. When P(H2O) is less than 1 atm, the rate of evaporation exceeds the rate of condensation. When P(H2O) is greater than 1 atm, the rate of condensation exceeds the rate of evaporation. Only when P(H2O) = 1 atm will evaporation and condensation occur at the same rate, so there will be no net exchange of material between the liquid and gaseous phases.
 
  • #9
Kqwert said:
Thank you!
isn't it wrong to write the equation with a "=" sign between the reactants and products then?
I think it would have been better if they had used an arrow. ---->
 

1. What is Gibbs free energy?

Gibbs free energy is a thermodynamic quantity that measures the amount of energy available to do useful work in a system at a constant temperature and pressure. It takes into account both the enthalpy (heat content) and entropy (degree of disorder) of a system.

2. How is Gibbs free energy related to spontaneity?

Gibbs free energy is closely related to spontaneity in chemical reactions. If the Gibbs free energy change (ΔG) is negative, the reaction is spontaneous and will proceed in the forward direction. If ΔG is positive, the reaction is non-spontaneous and will not occur without an input of energy. A ΔG of zero indicates that the reaction is at equilibrium.

3. What is the equation for calculating Gibbs free energy?

The equation for Gibbs free energy is ΔG = ΔH - TΔS, where ΔH is the change in enthalpy, T is the temperature in Kelvin, and ΔS is the change in entropy.

4. How is Gibbs free energy used in chemical reactions?

Gibbs free energy is used to determine whether a chemical reaction will occur spontaneously or not. It can also be used to calculate the maximum amount of work that can be obtained from a reaction. In addition, the change in Gibbs free energy can be used to predict the direction of a reaction at different temperatures.

5. What are the units of Gibbs free energy?

The units of Gibbs free energy are joules (J) in the International System of Units (SI). In chemistry, it is often expressed in kilojoules per mole (kJ/mol).

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