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The standard free energy change (ΔG°) for 50% dissociation of N2O4 into NO2 at 27 °C and 1 atm pressure is −x J mol−1 . The value of x

Question

The standard free energy change ΔG \Delta G^\circ for 50% dissociation of N2O4 into NO2 at 27 °C and 1 atm pressure is −x J mol−1 . The value of x

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Solution

To find the value of x x corresponding to the standard free energy change (ΔG° \Delta G° ) for the dissociation of N2O4 \text{N}_2\text{O}_4 into NO2 \text{NO}_2 at a given temperature, we can utilize the relationship between free energy change and equilibrium constant, along with the ideal gas law.

1. Break Down the Problem

  • The reaction of interest is: N2O4(g)2NO2(g) \text{N}_2\text{O}_4 (g) \rightleftharpoons 2 \text{NO}_2 (g)
  • We know that at 50% dissociation, the concentrations at equilibrium can be considered:
    • Initial moles: 1 mole of N2O4 \text{N}_2\text{O}_4
    • Moles at Equilibrium: 0.5 moles of N2O4 \text{N}_2\text{O}_4 and 1 moles of NO2 \text{NO}_2

2. Relevant Concepts

  • The equilibrium constant K K at 50% dissociation can be calculated as: K=[NO2]2[N2O4]=(1)20.5=2 K = \frac{[\text{NO}_2]^2}{[\text{N}_2\text{O}_4]} = \frac{(1)^2}{0.5} = 2
  • The relationship between ΔG° \Delta G° and K K is given by the formula: ΔG°=RTlnK \Delta G° = -RT \ln K Where:
    • R R = 8.314 J/(mol·K) (universal gas constant)
    • T T = 27 °C + 273.15 = 300.15 K
    • K=2 K = 2

3. Analysis and Detail

  • Substituting the values into the formula: ΔG°=(8.314)(300.15)ln(2) \Delta G° = - (8.314) (300.15) \ln(2)
  • Calculate ln(2) \ln(2) : ln(2)0.693 \ln(2) \approx 0.693
  • Now substitute this back into the equation: ΔG°(8.314)(300.15)(0.693) \Delta G° \approx - (8.314) (300.15) (0.693)
  • Performing the calculations step-by-step:
    • Calculate 8.314×300.15 8.314 \times 300.15 : 8.314×300.152498.3 J 8.314 \times 300.15 \approx 2498.3 \text{ J}
    • Now multiply by 0.693 -0.693 : ΔG°2498.3×0.6931730.3 J \Delta G° \approx -2498.3 \times 0.693 \approx -1730.3 \text{ J}

4. Verify and Summarize

  • After performing the calculations and verifying each step:
    • The calculated x x is therefore approximately 1730.3 1730.3 J mol1^{-1}.

Final Answer

The value of x x is 1730.3 1730.3 J mol1^{-1}.

This problem has been solved

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