This reaction is exothermic (since the enthalpy is negative). According to Le Chatelier's Principle, to increase the equilibrium concentration of SO\(_3\), we need to favor the formation of SO\(_3\) in the reaction.
Step 1: Effect of temperature - Since the reaction is exothermic, lowering the temperature will favor the production of SO\(_3\). At lower temperatures, the system will shift towards the products (SO\(_3\)) to release heat and restore equilibrium.
Step 2: Effect of pressure - The reaction involves a reduction in the number of gas molecules (from 3 moles of reactants to 2 moles of products). According to Le Chatelier's Principle, increasing the pressure will shift the equilibrium to the side with fewer gas molecules, which is the product side in this case.
Step 3: Conclusion The combination of higher pressure and lower temperature (Option B) will favor the production of SO\(_3\), as both conditions drive the reaction towards the product side.
Consider the gas phase reaction: \[ CO + \frac{1}{2} O_2 \rightleftharpoons CO_2 \] At equilibrium for a particular temperature, the partial pressures of \( CO \), \( O_2 \), and \( CO_2 \) are found to be \( 10^{-6} \, {atm} \), \( 10^{-6} \, {atm} \), and \( 16 \, {atm} \), respectively. The equilibrium constant for the reaction is ......... \( \times 10^{10} \) (rounded off to one decimal place).
Molten steel at 1900 K having dissolved hydrogen needs to be vacuum degassed. The equilibrium partial pressure of hydrogen to be maintained to achieve 1 ppm (mass basis) of dissolved hydrogen is ......... Torr (rounded off to two decimal places). Given: For the hydrogen dissolution reaction in molten steel \( \left( \frac{1}{2} {H}_2(g) = [{H}] \right) \), the equilibrium constant (expressed in terms of ppm of dissolved H) is: \[ \log_{10} K_{eq} = \frac{1900}{T} + 2.4 \] 1 atm = 760 Torr.
Consider the following reactions and their standard Gibbs free energies (in J): \[ {Fe(s)} + \frac{1}{2} {O}_2(g) \rightleftharpoons {FeO(s)} \quad \Delta G^\circ = -264900 + 65T \] \[ 2 {H}_2(g) + {O}_2(g) \rightleftharpoons 2 {H}_2{O(g)} \quad \Delta G^\circ = -492900 + 109T \] Assuming Fe and FeO to be pure and no solubility of gases in the solids, the value of \( \frac{p_{H_2O}}{p_{H_2}} \) required to reduce solid FeO to solid Fe at 1000 K is _________ (rounded off to two decimal places). Given: Ideal gas constant \( R = 8.314 \, {J mol}^{-1} {K}^{-1} \).
The reaction represented by \( A \rightarrow B \) follows first-order kinetics. At a given temperature, 20% of the reaction is completed in 223 s. The time taken to complete 50% of the reaction at the same temperature is _________ s (rounded off to the nearest integer).
Match the phenomena in Column I with the typical observations in Column II.
Radiative heat flux \( \dot{q} \) at a hot surface at a temperature \( T_s \) can be expressed as \[ \dot{q} = A f(T_s, T_\infty) (T_s - T_\infty) \] where \( A \) is a constant and \( T_\infty \) is the temperature of the surroundings (temperatures are expressed in K). The function \( f(T_s, T_\infty) \) is given by ______.
Match the steel plant related processes in Column I with the associated information in Column II.
Consider the phase diagram of a one-component system given below. \( V_{\alpha} \), \( V_{\beta} \), and \( V_{{Liquid}} \) are the molar volumes of \( \alpha \), \( \beta \), and liquid phases, respectively. Which one of the following statements is TRUE? Given: The change in molar enthalpies, \( \Delta H_{\alpha \to \beta} \) and \( \Delta H_{\beta \to {Liquid}} \), are positive.
For two continuous functions \( M(x, y) \) and \( N(x, y) \), the relation \( M dx + N dy = 0 \) describes an exact differential equation if