Step 1: Relationship Between \( K_p \) and \( K_c \)
The equilibrium constant \( K_p \) is defined using partial pressures, while \( K_c \) is defined using concentrations. The relationship is given by:
$$ K_p = K_c \left( RT \right)^{\Delta n} $$
Step 2: Condition for \( K_p \) and \( K_c \) Equality
For \( K_p \) to equal \( K_c \), \( \Delta n \) must be zero. This signifies an equal number of moles of gas on both sides of the chemical reaction.
Step 3: Analysis of Options
Option 1: \( H_2(g) + I_2(g) \rightleftharpoons 2HI(g) \)
Option 2: \( CO(g) + H_2O(g) \rightleftharpoons CO_2(g) + H_2(g) \)
Option 3: \( 2BrCl(g) \rightleftharpoons Br_2(g) + Cl_2(g) \)
Option 4: \( PCl_5(g) \rightleftharpoons PCl_3(g) + Cl_2(g) \)
Step 4: Conclusion
The correct option is: Option (4): \( PCl_5(g) \rightleftharpoons PCl_3(g) + Cl_2(g) \), because \( K_p eq K_c \).
37.8 g \( N_2O_5 \) was taken in a 1 L reaction vessel and allowed to undergo the following reaction at 500 K: \[ 2N_2O_5(g) \rightarrow 2N_2O_4(g) + O_2(g) \]
The total pressure at equilibrium was found to be 18.65 bar. Then, \( K_p \) is: Given: \[ R = 0.082 \, \text{bar L mol}^{-1} \, \text{K}^{-1} \]