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Solid Ca(HCO(3))(2) decomposes as Ca(H...

Solid `Ca(HCO_(3))_(2)` decomposes as
`Ca(HCO_(3))_(2)(s)hArrCaCO_(3)(s)+CO_(2)(g)+H_(2)O(g)`
If the total pressure is `0.2` bat at `420 K,` what is the standard free energy change for the given reaction `(Delta_(r)G^(@))` ?

A

`840 kJ//mol`

B

`3.86 kJ//mol`

C

`6.98 kJ//mol`

D

`16.083 kJ//mol`

Text Solution

AI Generated Solution

The correct Answer is:
To find the standard free energy change (ΔG°) for the decomposition of solid calcium bicarbonate (Ca(HCO₃)₂), we can follow these steps: ### Step 1: Write the balanced chemical equation The decomposition reaction is given as: \[ \text{Ca(HCO}_3\text{)}_2(s) \rightleftharpoons \text{CaCO}_3(s) + \text{CO}_2(g) + \text{H}_2O(g) \] ### Step 2: Identify the total pressure and the equilibrium condition It is given that the total pressure at equilibrium is \( P_{total} = 0.2 \, \text{bar} \) at \( T = 420 \, \text{K} \). ### Step 3: Determine the partial pressures of the gaseous products Since the reaction produces equal moles of CO₂ and H₂O, we can denote their partial pressures as: - \( P_{\text{CO}_2} = x \) - \( P_{\text{H}_2O} = x \) The total pressure is the sum of the partial pressures of the gaseous products: \[ P_{total} = P_{\text{CO}_2} + P_{\text{H}_2O} = x + x = 2x \] Setting this equal to the total pressure: \[ 2x = 0.2 \, \text{bar} \] Thus, \[ x = \frac{0.2}{2} = 0.1 \, \text{bar} \] So, \[ P_{\text{CO}_2} = 0.1 \, \text{bar} \] \[ P_{\text{H}_2O} = 0.1 \, \text{bar} \] ### Step 4: Calculate the equilibrium constant (Kp) The equilibrium constant \( K_p \) for the reaction is given by: \[ K_p = P_{\text{CO}_2} \times P_{\text{H}_2O} \] Substituting the values we found: \[ K_p = (0.1 \, \text{bar}) \times (0.1 \, \text{bar}) = 0.01 \, \text{bar}^2 \] ### Step 5: Use the relationship between ΔG° and Kp The standard free energy change is related to the equilibrium constant by the equation: \[ \Delta G° = -RT \ln K_p \] Where: - \( R = 8.314 \, \text{J/mol·K} \) - \( T = 420 \, \text{K} \) - \( K_p = 0.01 \) ### Step 6: Calculate ΔG° Substituting the values into the equation: \[ \Delta G° = - (8.314 \, \text{J/mol·K}) \times (420 \, \text{K}) \times \ln(0.01) \] Calculating \( \ln(0.01) \): \[ \ln(0.01) = -4.605 \] Now substituting this back: \[ \Delta G° = - (8.314 \times 420 \times -4.605) \] Calculating the product: \[ \Delta G° = 8.314 \times 420 \times 4.605 \] \[ \Delta G° \approx 16081.66 \, \text{J/mol} \] ### Step 7: Convert ΔG° to kilojoules To convert from joules to kilojoules: \[ \Delta G° = \frac{16081.66}{1000} \approx 16.082 \, \text{kJ/mol} \] ### Final Answer Thus, the standard free energy change for the given reaction is: \[ \Delta G° \approx 16.082 \, \text{kJ/mol} \] ---
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