G = Δh - Tδs: Spontaneity and Gibbs free energy
G = Δh - Tδs: Spontaneity and Gibbs free energy
G = Δh - Tδs: Spontaneity and Gibbs free energy
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At 298K:
ΔGϴreaction = ΔGϴf (products) – ΔGϴf (reactants)
At any temperature:
G = ΔH - TΔS
1. What is the standard free energy change, ∆GƟ, in kJ, for the following reaction at
298K?
2. A reaction has a standard enthalpy change, ΔH, of +10.00 kJ mol-1 at 298 K. The
standard entropy change, ΔS, for the same reaction is +10.00 J K-1 mol-1. What is the
value of ΔG for the reaction in kJ mol-1?
At 500 K, ∆H for this reaction is +177 kJmol-1 and ∆S is 161 J K-1 mol-1
(a) Explain why ∆H for the reaction above cannot be described as ΔHfƟ
(c) Calculate the value of ∆G at 500 K and determine, giving a reason, whether or
not the reaction will be spontaneous.
(i) The absolute entropy values, S, at 238 K for N2(g), H2(g) and NH3(g) are 192, 131
and 193 J K-1 mol-1 respectively. Calculate ∆SƟ for the reaction and explain the
sign of ∆SƟ.
(ii) Calculate ∆Gο for the reaction at 238 K. State and explain whether the
reaction is spontaneous.
5. Hex-1-ene gas, C6H12, burns in oxygen to produce carbon dioxide and water vapour.
(b) Use the data below to calculate the values of ΔHCƟ and ΔSƟ for the
combustion of hex-1-ene.
(c) Calculate the standard free energy change for the combustion of hex-1-ene.
(d) State and explain whether or not the combustion of hex-1-ene is spontaneous
at 25oC.
Answers:
3. (a) Cannot be ΔHfο as conditions are not standard and not formation from
elements.
(b) change in entropy/degree of disorder
4.
(i) ΔSƟ = [2×193] – [192 + 3×131] = –199 J K-1 mol-1
ΔSƟ is negative - four gaseous molecules forming two gaseous
molecules/fewer molecules of gas