/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 13 Suppose that the gas-phase react... [FREE SOLUTION] | 91Ó°ÊÓ

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Suppose that the gas-phase reactions \(\mathrm{A} \longrightarrow \mathrm{B}\) and \(\mathrm{B} \longrightarrow \mathrm{A}\) are both elementary processes with rate constants of \(4.7 \times 10^{-3} \mathrm{~s}^{-1}\) and \(5.8 \times 10^{-1} \mathrm{~s}^{-1}\), respectively. (a) What is the value of the equilibrium constant for the equilibrium \(\mathrm{A}(g) \rightleftharpoons \mathrm{B}(g) ?\) (b) Which is greater at equilibrium, the partial pressure of \(\mathrm{A}\) or the partial pressure of \(\mathrm{B}\) ? Explain.

Short Answer

Expert verified
(a) The equilibrium constant for the equilibrium A(g) ⇌ B(g) is 0.0081. (b) At equilibrium, the partial pressure of A is greater than the partial pressure of B.

Step by step solution

01

Write the given rate constants

We are given the rate constants for the elementary processes A → B and B → A: \(k_{AB} = 4.7 \times 10^{-3} \mathrm{s^{-1}}\) \(k_{BA} = 5.8 \times 10^{-1} \mathrm{s^{-1}}\)
02

Calculate the equilibrium constant

To find the equilibrium constant (K), we can use the relation: \(K = \frac{k_{AB}}{k_{BA}}\) Substitute the values into the equation: \(K = \frac{4.7 \times 10^{-3} \mathrm{s^{-1}}}{5.8 \times 10^{-1} \mathrm{s^{-1}}}\) Now calculate K: \(K = 0.0081\)
03

Analyze the ratio of equilibrium constant

We have found the equilibrium constant K = 0.0081. Now, let's analyze the equilibrium: If K = 1, then the concentrations of A and B are equal at equilibrium. If K < 1, then the concentration of A is greater than the concentration of B at equilibrium. If K > 1, then the concentration of B is greater than the concentration of A at equilibrium. In our case, the equilibrium constant K is less than 1 (K = 0.0081), so the concentration (and partial pressure) of A is greater than the concentration (and partial pressure) of B at equilibrium.
04

Write the final answer

(a) The equilibrium constant for the equilibrium A(g) ⇌ B(g) is 0.0081. (b) At equilibrium, the partial pressure of A is greater than the partial pressure of B.

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Key Concepts

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

Chemical Equilibrium
Understanding chemical equilibrium is vital for comprehending many chemical processes, including those that take place in industrial synthesizers and even in our own bodies. In simplest terms, chemical equilibrium occurs in a reversible reaction when the rate of the forward reaction is equal to the rate of the reverse reaction.

This balance does not mean that the reactants and products are present in equal amounts, but rather that their concentrations remain constant over time. At this point, a reaction may appear to have stopped, but in reality, both the forward and reverse reactions are still occurring – they are just doing so at the same rate, so there is no net change.

For the exercise relating to the reaction \(\mathrm{A}(g) \rightleftharpoons \mathrm{B}(g)\), we see this principle in action. With the rate constants given, we determined that the system reaches equilibrium when there is more A present than B, based on the value of the equilibrium constant.
Rate Constants
The concept of rate constants is fundamental to the kinetics of a chemical reaction – it determines the speed at which a reaction proceeds. It's important to remember that each elementary reaction has its own rate constant, symbolized by 'k'.

The rate constant is influenced by several factors: the nature of the reactants, the temperature, and the presence of a catalyst. In mathematical terms, for a simple one-step reaction, the rate of reaction is proportional to the product of the rate constant and the concentration of the reactants raised to a power equal to their stoichiometric coefficients.

In regards to our exercise, we had two opposing rate constants: \(k_{AB} = 4.7 \times 10^{-3} \mathrm{{s^{-1}}}\) for \(\mathrm{A} \rightarrow \mathrm{B}\), and \(k_{BA} = 5.8 \times 10^{-1} \mathrm{{s^{-1}}}\) for \(\mathrm{B} \rightarrow \mathrm{A}\). By comparing these rate constants, we can predict which direction the equilibrium will favor. Since the rate constant for the forward reaction is smaller than that for the reverse reaction, at equilibrium, we have a higher concentration of A, the reactant.
Partial Pressure
The concept of partial pressure is crucial when discussing reactions involving gases. It refers to the pressure that a single gas in a mixture would exert if it occupied the entire volume of the mixture at the same temperature. Think of it as a gas' contribution to the total pressure.In the context of chemical equilibrium of gases, the partial pressures of the reactants and products can be directly related to their concentrations by the ideal gas law. So, if you know the partial pressure of a gas, you can deduce its concentration at a given temperature and volume, making partial pressure a useful tool in equilibrium calculations.

For the problem at hand, understanding partial pressures helps us compare the amounts of A and B at equilibrium. Given that the equilibrium constant \(K\) is less than 1, it follows that the partial pressure of A will be greater than that of B. This is a direct consequence of A's higher concentration at equilibrium, a concept that might be confusing, but it becomes clearer once it is related directly to the reaction's equilibrium constant.

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Most popular questions from this chapter

Calculate \(K_{c}\) at \(303 \mathrm{~K}\) for \(\mathrm{SO}_{2}(g)+\mathrm{Cl}_{2}(g) \rightleftharpoons \mathrm{SO}_{2} \mathrm{Cl}_{2}(g)\) if \(K_{p}=34.5\) at this temperature.

Consider the hypothetical reaction \(\mathrm{A}(g)+2 \mathrm{~B}(g) \rightleftharpoons\) \(2 \mathrm{C}(g),\) for which \(K_{c}=0.25\) at a certain temperature. A \(1.00-\mathrm{L}\) reaction vessel is loaded with \(1.00 \mathrm{~mol}\) of compound \(\mathrm{C}\), which is allowed to reach equilibrium. Let the variable \(x\) represent the number of \(\mathrm{mol} / \mathrm{L}\) of compound A present at equilibrium. (a) In terms of \(x,\) what are the equilibrium concentrations of compounds \(\mathrm{B}\) and \(\mathrm{C} ?\) (b) What limits must be placed on the value of \(x\) so that all concentrations are positive? (c) By putting the equilibrium concentrations (in terms of \(x\) ) into the equilibrium-constant expression, derive an equation that can be solved for \(x\). (d) The equation from part (c) is a cubic equation (one that has the form \(\left.a x^{3}+b x^{2}+c x+d=0\right)\). In general, cubic equations cannot be solved in closed form. However, you can estimate the solution by plotting the cubic equation in the allowed range of \(x\) that you specified in part (b). The point at which the cubic equation crosses the \(x\) -axis is the solution. (e) From the plot in part (d), estimate the equilibrium concentrations of \(\mathrm{A}, \mathrm{B},\) and \(\mathrm{C}\).

Silver chloride, \(\mathrm{AgCl}(s)\), is an "insoluble" strong electrolyte. (a) Write the equation for the dissolution of \(\mathrm{AgCl}(s)\) in \(\mathrm{H}_{2} \mathrm{O}(l)\) (b) Write the expression for \(K_{c}\) for the reaction in part (a). (c) Based on the thermochemical data in Appendix \(\mathrm{C}\) and Le Châtelier's principle, predict whether the solubility of \(\mathrm{AgCl}\) in \(\mathrm{H}_{2} \mathrm{O}\) increases or decreases with increasing temperature. (d) The equilibrium constant for the dissolution of \(\mathrm{AgCl}\) in water is \(1.6 \times 10^{-10}\) at \(25^{\circ} \mathrm{C}\). In addition, \(\mathrm{Ag}^{+}(a q)\) can react with \(\mathrm{Cl}^{-}(a q)\) according to the reaction $$\mathrm{Ag}^{+}(a q)+2 \mathrm{Cl}^{-}(a q) \longrightarrow \mathrm{AgCl}_{2}^{-}(a q)$$ where \(K_{c}=1.8 \times 10^{5}\) at \(25^{\circ} \mathrm{C}\). Although \(\mathrm{AgCl}\) is "not soluble" in water, the complex \(\mathrm{AgCl}_{2}^{-}\) is soluble. At \(25^{\circ} \mathrm{C},\) is the solubility of AgCl in a \(0.100 M\) NaCl solution greater than the solubility of AgCl in pure water, due to the formation of soluble \(\mathrm{AgCl}_{2}^{-}\) ions? Or is the \(\mathrm{AgCl}\) solubility in \(0.100 \mathrm{M} \mathrm{NaCl}\) less than in pure water because of a Le Châtelier-type argument? Justify your answer with calculations.

A mixture of \(\mathrm{CH}_{4}\) and \(\mathrm{H}_{2} \mathrm{O}\) is passed over a nickel catalyst at \(1000 \mathrm{~K}\). The emerging gas is collected in a \(5.00-\mathrm{L}\) flask and is found to contain \(8.62 \mathrm{~g}\) of \(\mathrm{CO}, 2.60 \mathrm{~g}\) of \(\mathrm{H}_{2}, 43.0 \mathrm{~g}\) of \(\mathrm{CH}_{4},\) and \(48.4 \mathrm{~g}\) of \(\mathrm{H}_{2} \mathrm{O} .\) Assuming that equilibrium has been reached, calculate \(K_{c}\) and \(K_{p}\) for the reaction.

Methane, \(\mathrm{CH}_{4}\), reacts with \(\mathrm{I}_{2}\) according to the reaction \(\mathrm{CH}_{4}(g)+\mathrm{l}_{2}(g) \rightleftharpoons \mathrm{CH}_{3} \mathrm{l}(g)+\mathrm{HI}(g) .\) At \(630 \mathrm{~K}, K_{p}\) for this reaction is \(2.26 \times 10^{-4}\). A reaction was set up at \(630 \mathrm{~K}\) with initial partial pressures of methane of 105.1 torr and of 7.96 torr for \(\mathrm{I}_{2}\). Calculate the pressures, in torr, of all reactants and products at equilibrium.

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