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For the fuel cell reaction 2H(2)(g) +O(2...

For the fuel cell reaction `2H_(2)(g) +O_(2)(g) rarr 2H_(2)O(l), Deta_(f)H_(298)^(@) (H_(2)O,l) =- 285.5 kJ//mol` What is `Delta_(298)^(@)` for the given fuel cell reaction?
Given: `O_(2)(g) +4H^(+)(aQ) +4e^(-) rarr 2H_(2)O(l) E^(@) = 1.23 V`

A

`-0.322 J//K`

B

`-0.635 kJ//K`

C

`3.51 kJ//K`

D

`-0.322 kJ//K`

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The correct Answer is:
To solve the problem, we need to calculate the standard entropy change (ΔS₀) for the fuel cell reaction given by: \[ 2H_2(g) + O_2(g) \rightarrow 2H_2O(l) \] We are provided with the following information: - The standard enthalpy of formation of water, \( \Delta_f H_{298}^0(H_2O, l) = -285.5 \, \text{kJ/mol} \) - The cell reaction involves the half-reaction: \[ O_2(g) + 4H^+(aq) + 4e^- \rightarrow 2H_2O(l) \] with a standard cell potential \( E^0 = 1.23 \, \text{V} \). ### Step 1: Calculate ΔH₀ for the reaction Since the reaction produces 2 moles of water, we need to calculate the total enthalpy change for the formation of 2 moles of water: \[ \Delta H^0 = 2 \times \Delta_f H_{298}^0(H_2O, l) = 2 \times (-285.5 \, \text{kJ/mol}) = -571.0 \, \text{kJ} \] ### Step 2: Convert ΔH₀ to Joules Since we will be using Joules in our calculations, we convert ΔH₀ from kJ to J: \[ \Delta H^0 = -571.0 \, \text{kJ} = -571000 \, \text{J} \] ### Step 3: Calculate ΔG₀ using the electrochemical relationship Using the relationship from electrochemistry: \[ \Delta G^0 = -nFE^0 \] Where: - \( n = 4 \) (number of moles of electrons transferred) - \( F = 96500 \, \text{C/mol} \) (Faraday's constant) - \( E^0 = 1.23 \, \text{V} \) Calculating ΔG₀: \[ \Delta G^0 = -4 \times 96500 \, \text{C/mol} \times 1.23 \, \text{V} = -474780 \, \text{J} \] ### Step 4: Use the Gibbs free energy equation Using the Gibbs free energy equation: \[ \Delta G^0 = \Delta H^0 - T\Delta S^0 \] We can rearrange this to solve for ΔS₀: \[ \Delta S^0 = \frac{\Delta H^0 - \Delta G^0}{T} \] ### Step 5: Substitute the values Substituting the values we have: - \( \Delta H^0 = -571000 \, \text{J} \) - \( \Delta G^0 = -474780 \, \text{J} \) - \( T = 298 \, \text{K} \) \[ \Delta S^0 = \frac{-571000 - (-474780)}{298} \] Calculating the numerator: \[ \Delta S^0 = \frac{-571000 + 474780}{298} = \frac{-96220}{298} \] Calculating ΔS₀: \[ \Delta S^0 \approx -322.8 \, \text{J/K} \] ### Step 6: Convert ΔS₀ to kJ To convert to kJ: \[ \Delta S^0 \approx -0.3228 \, \text{kJ/K} \] ### Final Answer Thus, the standard entropy change for the given fuel cell reaction is approximately: \[ \Delta S^0 \approx -0.3228 \, \text{kJ/K} \]

To solve the problem, we need to calculate the standard entropy change (ΔS₀) for the fuel cell reaction given by: \[ 2H_2(g) + O_2(g) \rightarrow 2H_2O(l) \] We are provided with the following information: - The standard enthalpy of formation of water, \( \Delta_f H_{298}^0(H_2O, l) = -285.5 \, \text{kJ/mol} \) - The cell reaction involves the half-reaction: \[ O_2(g) + 4H^+(aq) + 4e^- \rightarrow 2H_2O(l) \] ...
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