When 100.0 \(\mathrm{mL}\) of 2.00 $\mathrm{M} \mathrm{Ce}\left(\mathrm{NO}_{3}\right)_{3}\( is added to 100.0 \)\mathrm{mL}$ of \(3.00 \mathrm{M} \mathrm{KIO}_{3},\) a precipitate of \(\mathrm{Ce}\left(\mathrm{IO}_{3}\right)_{3}(s)\) forms. Calculate the equilibrium concentrations of \(\mathrm{Ce}^{3+}\) and \(\mathrm{IO}_{3}^{-}\) in this solution. $\left[K_{\mathrm{sp}} \text { for } \mathrm{Ce}\left(\mathrm{IO}_{3}\right)_{3}=3.2 \times 10^{-10} .\right]$

Short Answer

Expert verified
The equilibrium concentrations are \([\mathrm{Ce}^{3+}]_{eq} = 0.9897\ \mathrm{M}\) and \([\mathrm{IO}_3^-]_{eq} = 1.468\ \mathrm{M}\).

Step by step solution

01

Write the balanced chemical equation for the precipitation reaction.

The balanced chemical equation for the precipitation reaction is: \[ \mathrm{Ce}^{3+}(aq) + 3 \mathrm{IO}_3^-(aq) \rightleftharpoons \mathrm{Ce(IO_3)_3}(s) \]
02

Calculate the initial concentrations for \(\mathrm{Ce}^{3+}\) and \(\mathrm{IO}_3^-\) ions.

To find the initial concentrations, we need to use the fact that the volumes of the two solutions are the same (100.0 mL) and that moles are additive. We can calculate the moles of each ion in the mixture: Moles of \(\mathrm{Ce}^{3+} = 100.0 \mathrm{mL} \times \frac{2.00 \mathrm{mol}}{1,000 \mathrm{mL}} = 0.200 \mathrm{mol}\) Moles of \(\mathrm{IO}_3^- = 100.0 \mathrm{mL} \times \frac{3.00 \mathrm{mol}}{1,000 \mathrm{mL}} = 0.300 \mathrm{mol}\) The volume of the mixture is the sum of the volumes of the two solutions: \(v = 100.0\mathrm{mL} + 100.0\mathrm{mL} = 200.0\mathrm{mL}\). The initial concentrations are calculated as: \[[\mathrm{Ce}^{3+}]_{initial} = \frac{0.200\ \mathrm{mol}}{200.0\ \mathrm{mL}} \times \frac{1,000\ \mathrm{mL}}{1\ \mathrm{mol}} = 1.00\ \mathrm{M}\] \[[\mathrm{IO}_3^-]_{initial} = \frac{0.300\ \mathrm{mol}}{200.0\ \mathrm{mL}} \times \frac{1,000\ \mathrm{mL}}{1\ \mathrm{mol}} = 1.50\ \mathrm{M}\]
03

Set up the ICE table.

Using the initial concentrations, we can set up an ICE table for the reaction: | | \(\mathrm{Ce}^{3+}(aq)\) | \(3\mathrm{IO}_3^-(aq)\) | \(\mathrm{Ce(IO_3)_3}(s)\) | | ------- | ---------------------- | --------------------- | ----------------------- | | Initial | 1.00 M | 1.50 M | solid | | Change | -x | -3x | +x | | Equilibrium | 1.00 M - x | 1.50 M - 3x | solid |
04

Write the expression for \(K_{sp}\) and solve for the equilibrium concentrations.

The solubility product constant \(K_{sp}\) expression is: \(K_{sp} = [\mathrm{Ce}^{3+}][\mathrm{IO}_3^-]^3\) Now, use the given value of \(K_{sp} = 3.2\times 10^{-10}\), and the values from the ICE table to solve for the equilibrium concentrations: \(3.2 \times 10^{-10} = (1.00\ \mathrm{M} - x) \times (1.50\ \mathrm{M} - 3x)^3\) By making the assumption that x is small enough compared to the initial values, we can simplify the equation to: \(3.2 \times 10^{-10} = \left(1.00\right) \times \left(1.50 - 3x\right)^3\) Now, solve for \(x\): \(x = 1.03\times10^{-2}\ \mathrm{M}\) Based on the ICE table, we have: \([\mathrm{Ce}^{3+}]_{eq} = 1.00\ \mathrm{M} - x = 1.00\ \mathrm{M} - 1.03\times10^{-2}\ \mathrm{M} = 0.9897\ \mathrm{M}\) \([\mathrm{IO}_3^-]_{eq} = 1.50\ \mathrm{M} - 3x = 1.50\ \mathrm{M} - 3(1.03\times10^{-2}\ \mathrm{M}) = 1.468\ \mathrm{M}\) So, the equilibrium concentrations are \([\mathrm{Ce}^{3+}]_{eq} = 0.9897\ \mathrm{M}\) and \([\mathrm{IO}_3^-]_{eq} = 1.468\ \mathrm{M}\).

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Most popular questions from this chapter

A friend tells you: "The constant \(K_{\mathrm{sp}}\) of a salt is called the solubility product constant and is calculated from the concentrations of ions in the solution. Thus, if salt A dissolves to a greater extent than salt \(\mathrm{B}\) , salt \(\mathrm{A}\) must have a higher \(K_{\mathrm{sp}}\) than salt \(\mathrm{B}\) ." Do you agree with your friend? Explain.

In the presence of \(\mathrm{CN}^{-}, \mathrm{Fe}^{3+}\) forms the complex ion \(\mathrm{Fe}(\mathrm{CN})_{6}^{3-} .\) The equilibrium concentrations of \(\mathrm{Fe}^{3+}\) and \(\mathrm{Fe}(\mathrm{CN})_{6}^{3-}\) are $8.5 \times 10^{-40} \mathrm{M}\( and \)1.5 \times 10^{-3} M,\( respectively, in a \)0.11-M$ KCN solution. Calculate the value for the overall formation constant of \(\mathrm{Fe}(\mathrm{CN})_{6}^{3-}\) . $$\mathrm{Fe}^{3+}(a q)+6 \mathrm{CN}^{-}(a q) \rightleftharpoons \mathrm{Fe}(\mathrm{CN})_{6}^{3-}(a q) \qquad K_{\text { overall }}=?$$

Aluminum ions react with the hydroxide ion to form the precipitate \(\mathrm{Al}(\mathrm{OH})_{3}(s),\) but can also react to form the soluble complex ion \(\mathrm{Al}(\mathrm{OH})_{4}^{-}.\) In terms of solubility, All \((\mathrm{OH})_{3}(s)\) will be more soluble in very acidic solutions as well as more soluble in very basic solutions. a. Write equations for the reactions that occur to increase the solubility of \(\mathrm{Al}(\mathrm{OH})_{3}(s)\) in very acidic solutions and in very basic solutions. b. Let's study the pH dependence of the solubility of \(\mathrm{Al}(\mathrm{OH})_{3}(s)\) in more detail. Show that the solubility of \(\mathrm{Al}(\mathrm{OH})_{3},\) as a function of \(\left[\mathrm{H}^{+}\right],\) obeys the equation $$S=\left[\mathrm{H}^{+}\right]^{3} K_{\mathrm{sp}} / K_{\mathrm{w}}^{3}+K K_{\mathrm{w}} /\left[\mathrm{H}^{+}\right]$$ where \(S=\) solubility \(=\left[\mathrm{Al}^{3+}\right]+\left[\mathrm{Al}(\mathrm{OH})_{4}^{-}\right]\) and \(K\) is the equilibrium constant for $$\mathrm{Al}(\mathrm{OH})_{3}(s)+\mathrm{OH}^{-}(a q) \rightleftharpoons \mathrm{Al}(\mathrm{OH})_{4}^{-}(a q)$$ c. The value of \(K\) is 40.0 and \(K_{\mathrm{sp}}\) for \(\mathrm{Al}(\mathrm{OH})_{3}\) is \(2 \times 10^{-32}\) Plot the solubility of \(\mathrm{Al}(\mathrm{OH})_{3}\) in the ph range \(4-12.\)

Two different compounds have about the same molar solubility. Do they also have about the same \(K_{\text {sp}}\) value?

Use the following data to calculate the \(K_{\mathrm{sp}}\) value for each solid. a. The solubility of \(\mathrm{CaC}_{2} \mathrm{O}_{4}\) is $4.8 \times 10^{-5} \mathrm{mol} / \mathrm{L}$ . b. The solubility of \(\mathrm{BiI}_{3}\) is $1.32 \times 10^{-5} \mathrm{mol} / \mathrm{L}$ .

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