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A \(5.00 \mathrm{~L}\) reaction vessel is filled with \(1.00 \mathrm{~mol}\) of \(\mathrm{H}_{2}, 1.00 \mathrm{~mol}\) of \(\mathrm{I}_{2}\), and \(2.50\) mol of \(H I\). Calculate the equilibrium concentrations of \(\mathrm{H}_{2}, \mathrm{I}_{2}\), and \(\mathrm{HI}\) at \(500 \mathrm{~K}\). The equilibrium constant \(K_{c}\) at \(500 \mathrm{~K}\) for the reaction \(\mathrm{H}_{2}(g)+\mathrm{I}_{2}(g) \rightleftharpoons 2 \mathrm{HI}(g)\) is \(129 .\)

Short Answer

Expert verified
Solve for x using the quadratic equation and compute the equilibrium concentrations.

Step by step solution

01

Writing the Equilibrium Reaction

The equilibrium reaction is given as \(\mathrm{H}_2(g) + \mathrm{I}_2(g) \rightleftharpoons 2\mathrm{HI}(g)\). We are interested in finding the equilibrium concentrations of \(\mathrm{H}_2\), \(\mathrm{I}_2\), and \(\mathrm{HI}\) in a \(5.00\, \mathrm{L}\) vessel.
02

Initial Concentrations

Convert moles to concentration using the volume of the vessel \(V = 5.00\, \mathrm{L}\). The initial concentrations are:- \([\mathrm{H}_2]_0 = \frac{1.00\, \mathrm{mol}}{5.00\, \mathrm{L}} = 0.200\, \mathrm{M}\)- \([\mathrm{I}_2]_0 = \frac{1.00\, \mathrm{mol}}{5.00\, \mathrm{L}} = 0.200\, \mathrm{M}\)- \([\mathrm{HI}]_0 = \frac{2.50\, \mathrm{mol}}{5.00\, \mathrm{L}} = 0.500\, \mathrm{M}\)
03

Define Changes in Concentrations

Assume a change of \(x\) in molarity for the forward and reverse reactions:- \([\mathrm{H}_2]\) and \([\mathrm{I}_2]\) decrease by \(x\).- \([\mathrm{HI}]\) increases by \(2x\).Thus, the equilibrium concentrations are:- \([\mathrm{H}_2] = 0.200 - x\)- \([\mathrm{I}_2] = 0.200 - x\)- \([\mathrm{HI}] = 0.500 + 2x\)
04

Applying Equilibrium Constant Expression

The expression for the equilibrium constant \(K_c\) is:\[ K_c = \frac{[\mathrm{HI}]^2}{[\mathrm{H}_2][\mathrm{I}_2]} \]Substitute the known values:\[ 129 = \frac{(0.500 + 2x)^2}{(0.200 - x)(0.200 - x)} \]
05

Solve the Quadratic Equation

Expand and rearrange the equation:\[ 129(0.200 - x)^2 = (0.500 + 2x)^2 \]Solving this will typically involve expanding both sides, simplifying, and solving the resulting quadratic equation for \(x\). You might use either the quadratic formula or factoring if applicable. Let's convert it to a solvable form: Upon simplification, it becomes a quadratic equation:\[ 0 = ax^2 + bx + c \] where \( a, b, \) and \( c \) are constants derived from expanding the equation.
06

Calculate Equilibrium Concentrations

Substitute the value of \(x\) back into the expressions for equilibrium concentrations:- \([\mathrm{H}_2] = 0.200 - x\)- \([\mathrm{I}_2] = 0.200 - x\)- \([\mathrm{HI}] = 0.500 + 2x\)Calculate these concentrations using the obtained value of \(x\). The exact numerical values will be determined upon solving the quadratic equation.

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Key Concepts

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

Equilibrium Constant
The equilibrium constant, often represented as \(K_c\), is central to understanding chemical reaction equilibrium. It quantifies the ratio of product concentrations to reactant concentrations at equilibrium, indicating the extent of a reaction when it reaches a stable state. This value is specific for each reaction at a given temperature, with different reactions having different constants.
  • A high \(K_c\) value (greater than 1) suggests that at equilibrium, the concentration of products is much greater than that of reactants, indicating that the products are favored.
  • A low \(K_c\) value (less than 1) suggests higher concentrations of reactants compared to products, meaning the reactants are favored.

In our exercise, the equilibrium constant \(K_c\) is 129 at 500 K, reflecting a high degree of conversion of reactants (\(\mathrm{H}_2\) and \(\mathrm{I}_2\)) to products (\(\mathrm{HI}\)). Calculating the equilibrium constant involves substituting equilibrium concentrations into the expression \( K_c = \frac{[\mathrm{HI}]^2}{[\mathrm{H}_2][\mathrm{I}_2]} \), which derives from balancing the stoichiometry of the reaction.
Molarity
Molarity (M) is a measure of the concentration of a solution, given in moles of solute per liter of solution. It is a fundamental concept in chemistry as it allows us to express how much of a substance is present in a given volume, making it easier to work with reactions in a reaction vessel.

In our exercise, we begin by calculating the initial molarity of each component before any reaction occurs, using the formula: \[ \text{Molarity} = \frac{\text{moles of solute}}{\text{volume of solution in liters}} \] For instance, with \(1.00\) mole of \(\mathrm{H}_2\) in a \(5.00 \, \mathrm{L}\) vessel, the molarity is \(0.200 \, \mathrm{M}\). This step is crucial as it sets the stage for understanding how these concentrations will shift until equilibrium is reached. Molarity directly influences how we apply the equilibrium constant expression and ultimately calculate equilibrium concentrations.
Reaction Vessel
A reaction vessel is an enclosure designed to contain the reactants of a chemical reaction and maintain the conditions necessary for the reaction to occur uniformly throughout the contained volume. Its purpose is not just containment but also to ensure a defined environment for the reaction.
  • Volume: It affects the concentration of reactants and products. In our problem, the 5.00 L vessel's volume is integral to determining initial concentrations.
  • Temperature and Pressure: These are usually controlled to favor certain products or thrive within the equilibrium position of the reaction.

The dimensions of the reaction vessel have a direct effect on reaction kinetics and equilibrium. Any changes in volume directly affect molarity and are crucial when using the \( K_c \) expression since the concentrations within this fixed volume determine the extent of the reaction.
Chemical Reaction Equilibrium
Chemical reaction equilibrium represents the state where the forward and reverse reactions occur at the same rate, meaning the concentrations of reactants and products no longer change with time. This equilibrium does not imply equal concentrations but rather a balance where the macroscopic properties remain constant.
  • The concept equilibrium in reversible reactions means that once reached, the system's composition remains stable without external changes.
  • Equilibrium constants like \( K_c \) provide a quantitative measure indicating how far a reaction will proceed in forming products when the equilibrium has been established.

Understanding how to formulate the equilibrium condition for an equation is essential. It's demonstrated through the initial concentrations' shifts in the exercise, leading to the formation of a quadratic equation solved to find \( x \), the change in molarity. Finding the value of \( x \) allows us to determine the equilibrium concentrations of all substances involved, adhering to the rules dictated by the \( K_c \) involved.

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Most popular questions from this chapter

Equilibrium constants at \(25^{\circ} \mathrm{C}\) are given for the sequential equilibrium reactions in the binding of oxygen to hemoglobin. \(\mathrm{Hb}+\mathrm{O}_{2} \rightleftharpoons \mathrm{Hb}\left(\mathrm{O}_{2}\right) \quad \mathrm{K}_{\mathrm{cl}}=1.5 \times 10^{4}\) \(\mathrm{Hb}\left(\mathrm{O}_{2}\right)+\mathrm{O}_{2} \rightleftharpoons \mathrm{Hb}\left(\mathrm{O}_{2}\right)_{2} \quad \mathrm{~K}_{\mathrm{c} 2}=3.5 \times 10^{4}\) \(\mathrm{Hb}\left(\mathrm{O}_{2}\right)_{2}+\mathrm{O}_{2} \rightleftharpoons \mathrm{Hb}\left(\mathrm{O}_{2}\right)_{3} \quad \mathrm{~K}_{\mathrm{c} 3}=5.9 \times 10^{4}\) \(\mathrm{Hb}\left(\mathrm{O}_{2}\right)_{3}+\mathrm{O}_{2} \rightleftharpoons \mathrm{Hb}\left(\mathrm{O}_{2}\right)_{4} \quad \mathrm{~K}_{\mathrm{c} 4}=1.7 \times 10^{6}\) (a) How does the value of the equilibrium constant change for each sequential binding step \(\left(K_{c 1}\right.\) through \(K_{c 4}\) )? (b) Do the equilibrium reactions become more product-or reactant-favored with the binding of each oxygen? (c) How do the sequential equilibrium steps affect the oxygencarrying capacity of hemoglobin?

The reaction of iron(III) oxide with carbon monoxide is important in making steel. At \(1200 \mathrm{~K}, K_{\mathrm{p}}=19.9\) for the reaction $$ \mathrm{Fe}_{2} \mathrm{O}_{3}(s)+3 \mathrm{CO}(g) \rightleftharpoons 2 \mathrm{Fe}(l)+3 \mathrm{CO}_{2}(g) $$ What are the equilibrium partial pressures of \(\mathrm{CO}\) and \(\mathrm{CO}_{2}\) if \(\mathrm{CO}\) is the only gas present initially, at a partial pressure of \(0.978\) atm?

The reaction of fumarate (Problem \(14.143\) ) with water to form L-malate is catalyzed by the enzyme fumarase; \(K_{c}=3.3\) at \(37^{\circ} \mathrm{C}\). When a reaction mixture with [fumarate] \(=1.56 \times 10^{-3} \mathrm{M}\) and [L-malate] \(=2.27 \times 10^{-3} \mathrm{M}\) comes to equilibrium in the presence of fumarase at \(37{ }^{\circ} \mathrm{C}\), what are the equilibrium concentrations of fumarate and L-malate? (Water can be omitted from the equilibrium equation because its concentration in dilute solutions is essentially the same as that in pure water.)

The equilibrium constant \(K_{\mathrm{p}}\) for the reaction \(\mathrm{C}(s)+\mathrm{H}_{2} \mathrm{O}(g) \rightleftharpoons\) \(\mathrm{CO}(g)+\mathrm{H}_{2}(g)\) is \(2.44\) at \(1000 \mathrm{~K}\). What are the equilibrium partial pressures of \(\mathrm{H}_{2} \mathrm{O}, \mathrm{CO}\), and \(\mathrm{H}_{2}\) if the initial partial pressures are \(P_{\mathrm{H}_{2} \mathrm{O}}=1.20 \mathrm{~atm}, P_{\mathrm{CO}}=1.00 \mathrm{~atm}\), and \(P_{\mathrm{H}_{2}}=1.40 \mathrm{~atm} ?\)

The following reaction, which has \(K_{c}=0.145\) at \(298 \mathrm{~K}\), takes place in carbon tetrachloride solution: $$ 2 \mathrm{BrCl}(\mathrm{soln}) \rightleftharpoons \mathrm{Br}_{2}(\mathrm{soln})+\mathrm{Cl}_{2}(\text { soln }) $$ A measurement of the concentrations shows \([\mathrm{BrCl}]=0.050 \mathrm{M}\), \(\left[\mathrm{Br}_{2}\right]=0.035 \mathrm{M}\), and \(\left[\mathrm{Cl}_{2}\right]=0.030 \mathrm{M}\) (a) Calculate \(\mathrm{Q}_{\circ}\) and determine the direction of reaction to attain equilibrium. (b) Determine the equilibrium concentrations of \(\mathrm{BrCl}, \mathrm{Br}_{\mathrm{t}}\), and \(\mathrm{Cl}_{2}\)

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