Consider a solution made by mixing \(500.0 \mathrm{~mL}\) of \(4.0 \mathrm{M} \mathrm{NH}_{3}\) and \(500.0 \mathrm{~mL}\) of \(0.40 \mathrm{M} \mathrm{AgNO}_{3} \cdot \mathrm{Ag}^{+}\) reacts with \(\mathrm{NH}_{3}\) to form \(\begin{aligned} \mathrm{AgNH}_{3}{ }^{+} \text {and } \mathrm{Ag}\left(\mathrm{NH}_{3}\right)_{2}+: \\ \mathrm{Ag}^{+}(a q)+\mathrm{NH}_{3}(a q) \rightleftharpoons \mathrm{AgNH}_{3}{ }^{+}(a q) & K_{1}=2.1 \times 10^{3} \\ \mathrm{AgNH}_{3}^{+}(a q)+\mathrm{NH}_{3}(a q) \rightleftharpoons \mathrm{Ag}\left(\mathrm{NH}_{3}\right)_{2}^{+}(a q) & K_{2}=8.2 \times 10^{3} \end{aligned}\) Determine the concentration of all species in solution.

Short Answer

Expert verified
The equilibrium concentrations of the species in the solution are approximately: \[ \mathrm{[NH_{3}]} \approx 1.801 \mathrm{~M} \] \[ \mathrm{[Ag^{+}]} \approx 0.020 \mathrm{~M} \] \[ \mathrm{[AgNH_{3}^{+}]} \approx 0.18 \mathrm{~M} \] \[ \mathrm{[Ag(NH_{3})_{2}^{+}]} \approx 0.019 \mathrm{~M} \]

Step by step solution

01

Calculate the initial concentration of the species

We are given the initial volumes and molarities of NH3 and AgNO3. To find the initial concentration of the species, we can use the formula: C1V1 + C2V2 = Ct Vt Where C1, C2 are the initial molarities, V1, V2 are the initial volumes, Ct is the final molarity, and Vt is the final volume. Since both solutions have volumes of 500 mL, we can add them up to get the final volume (Vt): Final Volume (Vt) = 500 mL + 500 mL = 1000 mL (1 L) Next, we need to find the initial concentration of NH3 and Ag+: For NH3: Initial concentration = (4.0 M)(0.5 L) / (1 L) = 2.0 M For Ag+: Initial concentration = (0.40 M)(0.5 L) / (1 L) = 0.20 M The initial concentrations of AgNH3+ and Ag(NH3)2+ are zero, as these species are produced by the reactions.
02

Create an ICE table

An ICE table (Initial, Change, Equilibrium) shows the initial concentration, the change in concentration during the reaction, and the equilibrium concentration of all species involved in the reaction. Let's denote the initial concentrations of NH3, Ag+, AgNH3+, and Ag(NH3)2+ as [NH3]0, [Ag+]0, [AgNH3+]0, and [Ag(NH3)2+]0, respectively. Now, let's denote the change in their concentrations as x, y, and z, respectively, as per the reactions: Ag+(aq) + NH3(aq) ⇌ AgNH3+(aq) with K1 = 2.1 x 10^3 AgNH3+(aq) + NH3(aq) ⇌ Ag(NH3)2+(aq) with K2 = 8.2 x 10^3 We can now create an ICE table: Species: NH3 | Ag+ | AgNH3+ | Ag(NH3)2+ -------------------------------------------------------- Initial: 2.0 M | 0.20 M | 0 M | 0 M Change: -x-y | -x | x | y Equilibrium: 2-x-y | 0.20-x | x | y
03

Write the expressions for the equilibrium constants and solve for x and y

Now, we will use the equilibrium constants (K1 and K2) to create expressions for the equilibrium concentrations of the species. K1 = [AgNH3+]/([Ag+][NH3]) = x/(0.20-x)(2-x-y) K2 = [Ag(NH3)2+]/([AgNH3+][NH3]) = y/(x(2-x-y)) Now, we can use the given values for K1 and K2 to solve for x and y: 2.1 x 10^3 = x/(0.20-x)(2-x-y) 8.2 x 10^3 = y/(x(2-x-y)) Solving these equations simultaneously for x and y, we get: x ≈ 0.18 M y ≈ 0.019 M
04

Calculate the equilibrium concentrations

We can now use the values of x and y to find the equilibrium concentrations of all species: [NH3] = 2.0 - x - y = 2.0 - 0.18 - 0.019 ≈ 1.801 M [Ag+] = 0.20 - x = 0.20 - 0.18 ≈ 0.020 M [AgNH3+] = x = 0.18 M [Ag(NH3)2+] = y = 0.019 M Therefore, the equilibrium concentrations of all species in the solution are approximately: [NH3] = 1.801 M [Ag+] = 0.020 M [AgNH3+] = 0.18 M [Ag(NH3)2+] = 0.019 M

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Most popular questions from this chapter

Calculate the solubility of each of the following compounds in moles per liter. Ignore any acid-base properties. a. \(\mathrm{PbI}_{2}, K_{\mathrm{sp}}=1.4 \times 10^{-8}\) b. \(\mathrm{CdCO}_{3}, K_{\text {sp }}=5.2 \times 10^{-12}\) c. \(\mathrm{Sr}_{3}\left(\mathrm{PO}_{4}\right)_{2}, K_{\text {sp }}=1 \times 10^{-31}\)

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Calculate the solubility of each of the following compounds in moles per liter. Ignore any acid-base properties. a. \(\mathrm{Ag}_{3} \mathrm{PO}_{4}, K_{\mathrm{sp}}=1.8 \times 10^{-18}\) b. \(\mathrm{CaCO}_{3}, K_{\mathrm{sp}}=8.7 \times 10^{-9}\) c. \(\mathrm{Hg}_{2} \mathrm{Cl}_{2}, K_{\mathrm{sp}}=1.1 \times 10^{-18}\left(\mathrm{Hg}_{2}^{2+}\right.\) is the cation in solution.)

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a. Calculate the molar solubility of \(\mathrm{Sr} \mathrm{F}_{2}\) in water, ignoring the basic properties of \(\mathrm{F}^{-} .\left(\right.\) For \(\mathrm{SrF}_{2}, K_{\text {sp }}=7.9 \times 10^{-10}\).) b. Would the measured molar solubility of \(\mathrm{Sr} \mathrm{F}_{2}\) be greater than or less than the value calculated in part a? Explain. c. Calculate the molar solubility of \(\mathrm{SrF}_{2}\) in a solution buffered at \(\mathrm{pH}=2.00 .\left(K_{\mathrm{a}}\right.\) for \(\mathrm{HF}\) is \(\left.7.2 \times 10^{-4} .\right)\)

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