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The standard enthalpy of formation of ga...

The standard enthalpy of formation of gaseous `H_(2)O` at 298 K is `-241.82` kJ/mol. Calculate `DeltaH^(@)` at 373 K given the following values of the molar heat capacities at constant pressure :
`H_(2)O(g)=33.58 " JK"^(-1)" mol"^(-1), " "H_(2)(g)=29.84 " JK"^(-1)" mol"^(-1), " "O_(2)(g)=29.37 " JK"^(-1)" mol"^(-1)`
Assume that the heat capacities are independent of temperature :

A

`-242.6 kJ//mol`

B

`-485.2 kJ//mol`

C

`-121.3 kJ//mol`

D

`-286.4 kJ//mol`

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The correct Answer is:
To solve the problem, we will follow these steps: ### Step 1: Calculate the change in heat capacity (ΔCp) We need to calculate the change in heat capacity for the reaction: \[ \text{H}_2(g) + \frac{1}{2} \text{O}_2(g) \rightarrow \text{H}_2O(g) \] The change in heat capacity (ΔCp) is given by: \[ \Delta Cp = Cp_{\text{products}} - Cp_{\text{reactants}} \] Where: - \( Cp_{\text{products}} = Cp_{\text{H}_2O(g)} = 33.58 \, \text{J K}^{-1} \text{mol}^{-1} \) - \( Cp_{\text{reactants}} = Cp_{\text{H}_2(g)} + \frac{1}{2} Cp_{\text{O}_2(g)} \) Calculating \( Cp_{\text{reactants}} \): \[ Cp_{\text{reactants}} = 29.84 \, \text{J K}^{-1} \text{mol}^{-1} + \frac{1}{2} \times 29.37 \, \text{J K}^{-1} \text{mol}^{-1} \] Calculating \( \frac{1}{2} \times 29.37 \): \[ \frac{1}{2} \times 29.37 = 14.685 \, \text{J K}^{-1} \text{mol}^{-1} \] Now substituting back: \[ Cp_{\text{reactants}} = 29.84 + 14.685 = 44.525 \, \text{J K}^{-1} \text{mol}^{-1} \] Now we can find ΔCp: \[ \Delta Cp = 33.58 - 44.525 = -10.945 \, \text{J K}^{-1} \text{mol}^{-1} \] ### Step 2: Use Kirchhoff's equation to find ΔH at 373 K Kirchhoff's equation is: \[ \Delta H(T_2) - \Delta H(T_1) = \Delta Cp \cdot (T_2 - T_1) \] Where: - \( T_1 = 298 \, \text{K} \) - \( T_2 = 373 \, \text{K} \) - \( \Delta H(T_1) = -241.82 \, \text{kJ/mol} \) Substituting the values into Kirchhoff's equation: \[ \Delta H(373) - (-241.82) = -10.945 \cdot (373 - 298) \] Calculating \( (373 - 298) \): \[ 373 - 298 = 75 \, \text{K} \] Now substituting this back into the equation: \[ \Delta H(373) + 241.82 = -10.945 \cdot 75 \] Calculating \( -10.945 \cdot 75 \): \[ -10.945 \cdot 75 = -821.625 \, \text{J/mol} = -0.821625 \, \text{kJ/mol} \] Now substituting this back into the equation: \[ \Delta H(373) + 241.82 = -0.821625 \] Solving for \( \Delta H(373) \): \[ \Delta H(373) = -0.821625 - 241.82 \] Calculating this: \[ \Delta H(373) = -242.641625 \, \text{kJ/mol} \] ### Step 3: Round to appropriate significant figures Rounding this to three significant figures gives: \[ \Delta H(373) \approx -242.64 \, \text{kJ/mol} \] ### Final Answer \[ \Delta H(373) \approx -242.64 \, \text{kJ/mol} \] ---

To solve the problem, we will follow these steps: ### Step 1: Calculate the change in heat capacity (ΔCp) We need to calculate the change in heat capacity for the reaction: \[ \text{H}_2(g) + \frac{1}{2} \text{O}_2(g) \rightarrow \text{H}_2O(g) \] ...
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