Always include the ∆ngRT correction term in bomb calorimetry problems when calcu lating thermodynamic equilibrium parameters
The thermodynamic relationship is given by:
\( \Delta G = \Delta H - T\Delta S \)
At equilibrium, \( \Delta G = 0 \), so:
\( T\Delta S = \Delta H - \Delta n_gRT \)
The reaction gives:
\( \Delta n_g = \text{moles of gaseous products} - \text{moles of gaseous reactants} \)
From the reaction:
\( \Delta n_g = 2 - \frac{7}{2} = -\frac{3}{2} \)
\( T\Delta S = -1406 + \left(-\frac{3}{2} \cdot 0.0083 \cdot 300 \right) \)
\( T\Delta S = -1406 + (-3.735) \)
\( T\Delta S \approx -1409.735 \, \text{kJ} \)
\( T\Delta S \approx -1411 \, \text{kJ} \)
The minimum value of \( T\Delta S \) needed to reach equilibrium is: \( 1411 \, \text{kJ}. \)
For the reaction A(g) $\rightleftharpoons$ 2B(g), the backward reaction rate constant is higher than the forward reaction rate constant by a factor of 2500, at 1000 K.
[Given: R = 0.0831 atm $mol^{–1} K^{–1}$]
$K_p$ for the reaction at 1000 K is:
The equilibrium constant for decomposition of $ H_2O $ (g) $ H_2O(g) \rightleftharpoons H_2(g) + \frac{1}{2} O_2(g) \quad (\Delta G^\circ = 92.34 \, \text{kJ mol}^{-1}) $ is $ 8.0 \times 10^{-3} $ at 2300 K and total pressure at equilibrium is 1 bar. Under this condition, the degree of dissociation ($ \alpha $) of water is _____ $\times 10^{-2}$ (nearest integer value). [Assume $ \alpha $ is negligible with respect to 1]
A square loop of sides \( a = 1 \, {m} \) is held normally in front of a point charge \( q = 1 \, {C} \). The flux of the electric field through the shaded region is \( \frac{5}{p} \times \frac{1}{\varepsilon_0} \, {Nm}^2/{C} \), where the value of \( p \) is: