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Ammonium iodide dissociates reversibly to ammonia and hydrogen iodide if the salt is heated to a sufficiently high temperature. $$ \mathrm{NH}_{4}\left[(\mathrm{s}) \rightleftharpoons \mathrm{NH}_{3}(\mathrm{g})+\mathrm{HI}(\mathrm{g})\right. $$ Some ammonium iodide is placed in a flask, which is then heated to \(400^{\circ} \mathrm{C}\). If the total pressure in the flask when equilibrium has been achieved is \(705 \mathrm{mm} \mathrm{Hg},\) what is the value of \(K_{\mathrm{p}}\) (when partial pressures are in atmospheres)?

Short Answer

Expert verified
\( K_\mathrm{p} \approx 0.214 \, \mathrm{atm}^2 \)

Step by step solution

01

Understanding the dissociation reaction

The given reaction is the dissociation of ammonium iodide (\( \mathrm{NH}_4\mathrm{I} \)) into ammonia (\( \mathrm{NH}_3 \)) and hydrogen iodide (\( \mathrm{HI} \)). The equilibrium equation is \( \mathrm{NH}_4\mathrm{I}_{(s)} \rightleftharpoons \mathrm{NH}_3_{(g)} + \mathrm{HI}_{(g)} \). At equilibrium, the partial pressures of the gaseous products are required to calculate \( K_\mathrm{p} \).
02

Relating total pressure to partial pressures

The total pressure at equilibrium is given as \( 705 \, \mathrm{mmHg} \), which converts to atmospheres as \( \frac{705}{760} \, \mathrm{atm} \). For each mole of \( \mathrm{NH}_3 \) produced, one mole of \( \mathrm{HI} \) is also produced, resulting in equal partial pressures of both gases.
03

Calculating equilibrium partial pressures

Let the equilibrium partial pressure of \( \mathrm{NH}_3 \) be \( P \). Then the partial pressure of \( \mathrm{HI} \) will also be \( P \). The total pressure is the sum of these partial pressures, thus: \( 2P = \frac{705}{760} \). Calculate \( P \) using this equation.
04

Solve for \( P \)

Solving \( 2P = \frac{705}{760} \), you get \( P = \frac{705}{1520} \). Compute this value.
05

Calculate \( K_\mathrm{p} \)

The equilibrium constant \( K_\mathrm{p} \) for the reaction is given by the expression \( K_\mathrm{p} = (P_{\mathrm{NH}_3})(P_{\mathrm{HI}}) = P^2 \). Substitute the value of \( P \) from Step 4 into this equation to find \( K_\mathrm{p} \).

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Key Concepts

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

Dissociation Reaction
A dissociation reaction involves the breaking apart of a compound into two or more components. In our example, ammonium iodide (\( \mathrm{NH}_4\mathrm{I} \)) undergoes dissociation when heated to form ammonia (\( \mathrm{NH}_3 \)) and hydrogen iodide (\( \mathrm{HI} \)). This is a reversible reaction, meaning that it can proceed in both forward and backward directions, reaching a point of equilibrium. At this point, the rate of dissociation equals the rate of re-formation of ammonium iodide. Understanding the characteristics of dissociation reactions is key:
  • They often require energy, such as heat, to proceed.
  • They are described by a chemical equation showing the conversion from a compound to simpler products.
  • In equilibrium, the concentration of reactants and products remains constant over time.
The specific reaction in this exercise is represented as:\[ \mathrm{NH}_4\mathrm{I}_{(s)} \rightleftharpoons \mathrm{NH}_3_{(g)} + \mathrm{HI}_{(g)} \]Here, solid ammonium iodide dissociates into gaseous products. The balance of this reaction at equilibrium is important for determining various properties, such as the equilibrium constant.
Equilibrium Constant (Kp)
The equilibrium constant (\( K_p \)) provides a quantitative measure of the position of equilibrium in a chemical reaction involving gases, and it is expressed in terms of partial pressures. For our dissociation of ammonium iodide, \( K_p \) represents the ratio of the product of the partial pressures of the gases at equilibrium. It is expressed as:\[ K_p = (P_{\mathrm{NH}_3})(P_{\mathrm{HI}}) = P^2 \]Here, \( P \) represents the partial pressure of both ammonia and hydrogen iodide since they are produced in equal amounts during the reaction.To calculate \( K_p \):
  • Understand that the total pressure at equilibrium is the sum of the partial pressures of \( \mathrm{NH}_3 \) and \( \mathrm{HI} \).
  • Convert the given total pressure from mmHg to atmospheres for compatibility with \( K_p \) calculations. In this case, the total pressure is \( 705 \ \mathrm{mmHg} \) converted to \( \frac{705}{760} \ \mathrm{atm} \).
  • Determine the partial pressure of each gas (\( P \)) using \( 2P = \frac{705}{760} \), resulting in \( P = \frac{705}{1520} \).
  • Substitute back the value of \( P \) to find \( K_p \).
Having \( K_p \) is crucial as it tells us how far a reaction has proceeded and the relative amounts of reactants and products at equilibrium.
Partial Pressure
Partial pressure describes the pressure exerted by a single gas in a mixture of gases. It is a crucial concept in understanding gas mixtures, especially in equilibrium reactions like the one involving \( \mathrm{NH}_4\mathrm{I} \) dissociation. The total pressure in a container is the sum of the partial pressures of each gas present. To determine partial pressures at equilibrium:
  • Recognize that each component in the gas mixture contributes to the total pressure based on its mole fraction.
  • In the given reaction, ammonia and hydrogen iodide contribute equally to the pressure. Therefore, we let the partial pressure of \( \mathrm{NH}_3 \) be \( P \) and \( \mathrm{HI} \) will also have \( P \) as its partial pressure.
  • Relate the total pressure to individual partial pressures using the equation for total pressure: \( P_{\text{total}} = P_{\mathrm{NH}_3} + P_{\mathrm{HI}} = 2P \).
  • Use this relationship to solve for \( P \), which is \( \frac{705}{1520} \) in this exercise after converting total pressure to atmospheres.
For chemical reactions and calculations involving gases, knowing the partial pressures helps in determining other properties such as reaction rates and equilibrium constants.

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Most popular questions from this chapter

Characterize each of the following as product- or reactant-favored at equilibrium. $$\begin{aligned} &\text { (a) } \mathrm{CO}(\mathrm{g})+1 / 2 \mathrm{O}_{2}(\mathrm{g}) \rightleftharpoons \mathrm{CO}_{2}(\mathrm{g})\\\ &&K_{\mathrm{p}}=1.2 \times 10^{45} \end{aligned}$$ $$\begin{aligned} &\text { (b) } \mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \rightleftharpoons \mathrm{H}_{2}(\mathrm{g})+1 / 2 \mathrm{O}_{2}(\mathrm{g})\\\ &&K_{\mathrm{p}}=9.1 \times 10^{-41} \end{aligned}$$ $$\begin{aligned} &\text { (c) } \mathrm{CO}(\mathrm{g})+\mathrm{Cl}_{2}(\mathrm{g}) \rightleftharpoons \mathrm{COCl}_{2}(\mathrm{g})\\\ &&K_{\mathrm{p}}=6.5 \times 10^{11} \end{aligned}$$

Sulfuryl chloride, \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\), is used as a reagent in the synthesis of organic compounds. When heated to a sufficiently high temperature, it decomposes to \(\mathrm{SO}_{2}\) and \(\mathrm{Cl}_{2}\) \(\mathrm{SO}_{2} \mathrm{Cl}_{2}(\mathrm{g}) \rightleftharpoons \mathrm{SO}_{2}(\mathrm{g})+\mathrm{Cl}_{2}(\mathrm{g}) \quad K_{\mathrm{c}}=0.045\) at \(375^{\circ} \mathrm{C}\) (a) \(A\) 10.0-L. flask containing 6.70 g of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) is heated to \(375^{\circ} \mathrm{C}\). What is the concentration of each of the compounds in the system when equilibrium is achieved? What fraction of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) has dissociated? (b) What are the concentrations of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}, \mathrm{SO}_{2}\) and \(\mathrm{Cl}_{2}\) at equilibrium in the 10.0 -L flask at \(375^{\circ} \mathrm{C}\) if you begin with a mixture of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) \((6.70 \mathrm{g})\) and \(\mathrm{Cl}_{2}(0.10 \mathrm{atm}) ?\) What fraction of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) has dissociated? (c) Compare the fractions of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) in parts (a) and (b). Do they agree with your expectations based on Le Chatelier's principle?

Suppose a tank initially contains \(\mathrm{H}_{2} \mathrm{S}\) at a pressure of 10.00 atm and a temperature of 800 K. When the reaction has come to equilibrium, the partial pressure of \(\mathbf{S}_{2}\) vapor is 0.020 atm. Calculate \(K_{\mathrm{p}}\) $$ 2 \mathrm{H}_{2} \mathrm{S}(\mathrm{g}) \rightleftharpoons 2 \mathrm{H}_{2}(\mathrm{g})+\mathrm{S}_{2}(\mathrm{g}) $$

The equilibrium constant, \(K_{c}\), for the reaction $$ \mathrm{N}_{2} \mathrm{O}_{4}(\mathrm{g}) \rightleftharpoons 2 \mathrm{NO}_{2}(\mathrm{g}) $$ at \(25^{\circ} \mathrm{C}\) is \(5.9 \times 10^{-3} .\) Suppose \(15.6 \mathrm{g}\) of \(\mathrm{N}_{2} \mathrm{O}_{4}\) is placed in a 5.000 -L flask at \(25^{\circ}\) C. Calculate the following: (a) the amount of \(\mathrm{NO}_{2}\) (mol) present at equilibrium; (b) the percentage of the original \(\mathrm{N}_{2} \mathrm{O}_{4}\) that is dissociated.

Hydrogen and carbon dioxide react at a high temperature to give water and carbon monoxide. $$ \mathrm{H}_{2}(\mathrm{g})+\mathrm{CO}_{2}(\mathrm{g}) \rightleftharpoons \mathrm{H}_{2} \mathrm{O}(\mathrm{g})+\mathrm{CO}(\mathrm{g}) $$ (a) Laboratory measurements at \(986^{\circ} \mathrm{C}\) show that there are 0.11 mol each of \(\mathrm{CO}\) and \(\mathrm{H}_{2} \mathrm{O}\) vapor and 0.087 mol each of \(\mathrm{H}_{2}\) and \(\mathrm{CO}_{2}\) at equilibrium in a 50.0 -L container. Calculate the equilibrium constant for the reaction at \(986^{\circ} \mathrm{C}\) (b) Suppose 0.010 mol each of \(\mathrm{H}_{2}\) and \(\mathrm{CO}_{2}\) are placed in a 200.0 -L. container. When equilibrium is achieved at \(986^{\circ} \mathrm{C},\) what amounts of \(\mathrm{CO}(\mathrm{g})\) and \(\mathrm{H}_{2} \mathrm{O}(\mathrm{g}),\) in moles, would be present? [Use the value of \(K_{c}\) from part (a).]

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