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Calculate the equilibrium constant K(p) ...

Calculate the equilibrium constant `K_(p)` and `K_(c )` for the reaction: `CO(g)+1//2O_(2)(g) hArr CO_(2)(g)`. Given that the partial pressure at equilibrium in a vessel at `3000 K` are `p_(CO)=0.4 atm, p_(CO_(2))=0.2 atm`

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To calculate the equilibrium constants \( K_p \) and \( K_c \) for the reaction: \[ \text{CO}(g) + \frac{1}{2}\text{O}_2(g) \rightleftharpoons \text{CO}_2(g) \] given the partial pressures at equilibrium: - \( p_{\text{CO}} = 0.4 \, \text{atm} \) - \( p_{\text{CO}_2} = 0.2 \, \text{atm} \) - \( p_{\text{O}_2} = 0.2 \, \text{atm} \) ### Step 1: Write the expression for \( K_p \) The equilibrium constant \( K_p \) for the reaction is given by the formula: \[ K_p = \frac{p_{\text{CO}_2}}{p_{\text{CO}} \cdot (p_{\text{O}_2})^{1/2}} \] ### Step 2: Substitute the known values into the \( K_p \) expression Substituting the given partial pressures into the equation: \[ K_p = \frac{0.2}{0.4 \cdot (0.2)^{1/2}} \] ### Step 3: Calculate \( (0.2)^{1/2} \) Calculating the square root of \( 0.2 \): \[ (0.2)^{1/2} = 0.4472 \, \text{(approximately)} \] ### Step 4: Substitute back into the \( K_p \) expression Now substitute this value back into the equation for \( K_p \): \[ K_p = \frac{0.2}{0.4 \cdot 0.4472} \] ### Step 5: Calculate the denominator Calculating the denominator: \[ 0.4 \cdot 0.4472 = 0.17888 \, \text{(approximately)} \] ### Step 6: Calculate \( K_p \) Now calculate \( K_p \): \[ K_p = \frac{0.2}{0.17888} \approx 1.118 \] ### Step 7: Calculate \( K_c \) To find \( K_c \), we can use the relationship between \( K_p \) and \( K_c \): \[ K_p = K_c (RT)^{\Delta n} \] Where: - \( R = 0.0821 \, \text{L atm/(K mol)} \) - \( T = 3000 \, \text{K} \) - \( \Delta n = \text{moles of gaseous products} - \text{moles of gaseous reactants} = 1 - (1 + \frac{1}{2}) = -\frac{1}{2} \) ### Step 8: Calculate \( K_c \) Substituting the values into the equation: \[ K_p = K_c \cdot (0.0821 \cdot 3000)^{-\frac{1}{2}} \] Calculating \( (0.0821 \cdot 3000)^{-\frac{1}{2}} \): \[ 0.0821 \cdot 3000 = 246.3 \] \[ (246.3)^{-\frac{1}{2}} \approx 0.0635 \] Now substituting back into the equation: \[ 1.118 = K_c \cdot 0.0635 \] Solving for \( K_c \): \[ K_c = \frac{1.118}{0.0635} \approx 17.6 \] ### Final Results Thus, the equilibrium constants are: \[ K_p \approx 1.118 \quad \text{and} \quad K_c \approx 17.6 \]

To calculate the equilibrium constants \( K_p \) and \( K_c \) for the reaction: \[ \text{CO}(g) + \frac{1}{2}\text{O}_2(g) \rightleftharpoons \text{CO}_2(g) \] given the partial pressures at equilibrium: ...
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