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Find out the value of K(c ) for each of ...

Find out the value of `K_(c )` for each of the following equilibrium from the value of `K_(p)`:
a. `2NOCl(g) hArr 2NO(g)+Cl_(2)(g), K_(p)=1.8xx10^(-2)` at `500 K`
b. `CaCO_(3)(s) hArr CaO(s)+CO_(2)(g), K_(p)=167` at `1073 K`

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To find the value of \( K_c \) from the given \( K_p \) values for the equilibria, we will use the relationship between \( K_p \) and \( K_c \): \[ K_p = K_c (RT)^{\Delta N_g} \] Where: - \( R \) is the ideal gas constant (0.0831 L·bar/(K·mol) or 0.0821 L·atm/(K·mol)) - \( T \) is the temperature in Kelvin - \( \Delta N_g \) is the change in the number of moles of gas, calculated as the moles of gaseous products minus the moles of gaseous reactants. ### Step 1: Calculate \( K_c \) for the first equilibrium **Given:** - Reaction: \( 2NOCl(g) \rightleftharpoons 2NO(g) + Cl_2(g) \) - \( K_p = 1.8 \times 10^{-2} \) at \( T = 500 \, K \) **Calculate \( \Delta N_g \):** - Moles of gaseous products = \( 2 \, (NO) + 1 \, (Cl_2) = 3 \) - Moles of gaseous reactants = \( 2 \, (NOCl) = 2 \) - \( \Delta N_g = 3 - 2 = 1 \) **Using the relationship:** \[ K_p = K_c (RT)^{\Delta N_g} \] \[ K_c = \frac{K_p}{(RT)^{\Delta N_g}} \] **Substituting values:** - \( R = 0.0831 \, L \cdot bar/(K \cdot mol) \) - \( T = 500 \, K \) \[ K_c = \frac{1.8 \times 10^{-2}}{(0.0831 \times 500)^1} \] \[ K_c = \frac{1.8 \times 10^{-2}}{41.55} \] \[ K_c \approx 4.33 \times 10^{-4} \] ### Step 2: Calculate \( K_c \) for the second equilibrium **Given:** - Reaction: \( CaCO_3(s) \rightleftharpoons CaO(s) + CO_2(g) \) - \( K_p = 167 \) at \( T = 1073 \, K \) **Calculate \( \Delta N_g \):** - Moles of gaseous products = \( 1 \, (CO_2) = 1 \) - Moles of gaseous reactants = \( 0 \) (since \( CaCO_3 \) is a solid) - \( \Delta N_g = 1 - 0 = 1 \) **Using the relationship:** \[ K_c = \frac{K_p}{(RT)^{\Delta N_g}} \] **Substituting values:** - \( R = 0.0831 \, L \cdot bar/(K \cdot mol) \) - \( T = 1073 \, K \) \[ K_c = \frac{167}{(0.0831 \times 1073)^1} \] \[ K_c = \frac{167}{89.05} \] \[ K_c \approx 1.87 \] ### Final Answers: - For the first equilibrium: \( K_c \approx 4.33 \times 10^{-4} \) - For the second equilibrium: \( K_c \approx 1.87 \)

To find the value of \( K_c \) from the given \( K_p \) values for the equilibria, we will use the relationship between \( K_p \) and \( K_c \): \[ K_p = K_c (RT)^{\Delta N_g} \] Where: - \( R \) is the ideal gas constant (0.0831 L·bar/(K·mol) or 0.0821 L·atm/(K·mol)) ...
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