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When sulphur (in the form of \(S_{8}\) ) is heated at temperature \(T\), at equilibrium, the pressure of \(S_{8}\) falls by \(30 \%\) from \(1.0 \mathrm{~atm}\), because \(\mathrm{S}_{8}(g)\) is partially converted into \(\mathrm{S}_{2}(g)\). Find the value of \(K_{p}\) for this reaction. (a) \(2.96\) (b) \(6.14\) (c) \(204.8\) (d) None of these

Short Answer

Expert verified
2.96

Step by step solution

01

- Understanding the chemical reaction

Assume initially there's 1 mole of \(S_8\) gas. During the process at equilibrium, as the pressure of \(S_8\) falls by 30\%, it means that 30\% of \(S_8\) has been converted into \(S_2\). The chemical equilibrium reaction can be expressed as: \(\text{S}_8(g) \rightleftharpoons 4\text{S}_2(g)\).
02

- Calculating the change in moles at equilibrium

If initially there is 1 mole of \(S_8\), at equilibrium there will be \((1 - 0.3) = 0.7\) moles of \(S_8\) left. Since for every mole of \(S_8\) that reacts, 4 moles of \(S_2\) are produced, the moles of \(S_2\) formed at equilibrium will be \((4 \times 0.3) = 1.2\) moles.
03

- Writing the expression for \(K_p\)

The expression for the equilibrium constant in terms of partial pressures \(K_p\) is given by \(K_p = \frac{(P_{S_{2}})^4}{P_{S_{8}}}\). Since the partial pressures are proportional to moles for a given volume and temperature, we can substitute moles for partial pressures in the \(K_p\) expression.
04

- Find the initial partial pressures

The initial partial pressure of \(S_8\) is 1 atm. Since no \(S_2\) is present initially, its partial pressure is 0 atm.
05

- Calculating the partial pressures at equilibrium

At equilibrium, the partial pressure of \(S_8\) is 30\% less than the initial value, so it's \((1.0 \, \text{atm} - 0.3 \times 1.0 \text{atm}) = 0.7 \, \text{atm}\). As the volume and temperature remain constant, the change in moles of \(S_2\) is directly proportional to the change in its partial pressure. Thus the partial pressure of \(S_2\) is \((1.2/1.0) \times 1.0 \, \text{atm} = 1.2 \, \text{atm}\).
06

- Plug in the values into the \(K_p\) expression

Insert the calculated equilibrium partial pressures in the \(K_p\) expression: \(K_p = \frac{(1.2 \, \text{atm})^4}{0.7 \, \text{atm}}\).
07

- Calculate \(K_p\)

Perform the calculations: \(K_p = \frac{1.2^4 \, \text{atm}^4}{0.7 \, \text{atm}} = \frac{2.0736 \, \text{atm}^4}{0.7 \, \text{atm}} = 2.96229 \, \text{atm}^3\). This value rounds off to 2.96.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Kp Calculation
Understanding how to calculate the equilibrium constant, represented as Kp, is crucial when exploring chemical equilibrium. Kp is based on the partial pressures of gases at equilibrium. For a balanced chemical equation of the form aA(g) + bB(g) ⇌ cC(g) + dD(g), Kp is determined using the expression:
Kp = \(\frac{(P_C)^c \cdot (P_D)^d}{(P_A)^a \cdot (P_B)^b}\) where P represents the partial pressures of components in atmosphere (atm) and a, b, c, d denote the stoichiometric coefficients. To solve for Kp, one must know or calculate the partial pressures of the reactants and products at the equilibrium state. For gaseous equilibria, as in the exercise, this involves a direct relation between the drop in the reactant's pressure and the formation of products' pressure.
Partial Pressure in Equilibrium
Partial pressure describes the pressure that each gas in a mixture would exert if it were alone in a container. At equilibrium, the sum of the partial pressures of all gases equals the total pressure. In our exercise, the initial total pressure is exerted solely by S8(g), and as it partially converts to S2(g), the partial pressures of both gases at equilibrium need to be accounted for. A 30% decline in the S8 pressure after equilibrium suggests a corresponding increase in the S2 pressure. The proportionality becomes handy as we can convert moles to pressure directly when volume and temperature are constant. This way, the partial pressures reflect the mole fractions of the gases, allowing one to apply them in the Kp expression to find the equilibrium constant.
Le Chatelier's Principle
Le Chatelier's principle helps predict how a system at equilibrium reacts to changes in concentration, temperature, or pressure. It states that if a dynamic equilibrium is disturbed, the system adjusts in a way that counteracts the change. For example, if the pressure were increased in the given exercise, the system would shift to reduce pressure, typically by favoring the reaction that produces fewer moles of gas. Consequently, understanding the shifts can provide insights on how the equilibrium concentrations or pressures might change. This adjustment is key to predicting how Kp may vary with the conditions and helps students understand that equilibrium states are not static but dynamic and responsive to external influences.
Mole-to-Mole Conversion in Chemical Reactions
In chemical reactions, the stoichiometry plays an integral role in establishing relationships between reactants and products. Mole-to-mole conversion is a process of using the balanced equation to understand these relationships. For instance, the reaction provided shows that 1 mole of S8(g) produces 4 moles of S2(g). Therefore, the conversion of S8 moles at equilibrium to S2 is pivotal for calculating the partial pressures that are used to find Kp. Understanding these conversions guides in determining how much of a reactant is needed to form a desired amount of product and is essential in quantifying the components at equilibrium.

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Most popular questions from this chapter

For the reaction \(2 \mathrm{NO}_{2}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \rightleftharpoons \mathrm{N}_{2} \mathrm{O}_{5}(\dot{g})\), if the equilibrium constant is \(K_{p}\), then the equilibrium constant for the reaction \(2 \mathrm{~N}_{2} \mathrm{O}_{5}(g) \rightleftharpoons 4 \mathrm{NO}_{2}(g)+\mathrm{O}_{2}(g)\) would be : (a) \(K_{p}^{2}\) (b) \(\frac{2}{K_{p}}\) (c) \(\frac{1}{K_{p}^{2}}\) (d) \(\frac{1}{\sqrt{K_{p}}}\)

If the pressure in a reaction vessel for the following reaction is increased by decreasing the volume, what will happen to the concentrations of \(\mathrm{CO}\) and \(\mathrm{CO}_{2}\) ? $$ \mathrm{H}_{2} \mathrm{O}(g)+\mathrm{CO}(g) \rightleftharpoons \mathrm{H}_{2}(g)+\mathrm{CO}_{2}(g)+\text { Heat } $$ (a) both the [CO] and [CO \(\left._{2}\right]\) will decrease (b) neither the [CO] nor the \(\left[\mathrm{CO}_{2}\right]\) will change (c) the [CO] will decrease and the [CO \(_{2}\) ] will increase (d) both the [CO] and [CO \(\left._{2}\right]\) will increase

The standard free energy change of a reaction is \(\Delta G^{\circ}=-115 \mathrm{~kJ}\) at \(298 \mathrm{~K}\). Calculate the value of \(\log _{10} K_{p}\left(R=8.314 \mathrm{JK}^{-1} \mathrm{~mol}^{-1}\right)\) (a) \(20.16\) (b) \(2.303\) (c) \(2.016\) (d) \(13.83\)

Two moles of \(\mathrm{NH}_{3}\) when put into a previously evacuated vessel (one litre), partially dissociated into \(\mathrm{N}_{2}\) and \(\mathrm{H}_{2}\). If at equilibrium one mole of \(\mathrm{NH}_{3}\) is present, the equilibrium constant is : (a) \(3 / 4 \mathrm{~mol}^{2}\) litre \(^{-2}\) (b) \(27 / 64 \mathrm{~mol}^{2}\) litre \(^{-2}\) (c) \(27 / 32 \mathrm{~mol}^{2}\) litre \(^{-2}\) (d) \(27 / 16 \mathrm{~mol}^{2}\) litre \(^{-2}\)

Using molar concentrations, what is the unit of \(K_{c}\) for the reaction? $$ \mathrm{CH}_{3} \mathrm{OH}(g) \rightleftharpoons \mathrm{CO}(g)+2 \mathrm{H}_{2}(g) $$ (a) \(M^{-2}\) (b) \(M^{2}\) (c) \(M^{-1}\) (d) \(M\)

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