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Solubility Showdown

An AP Chemistry lesson exploring solubility rules, net ionic equations, particulate representations, and the mathematical link to Ksp and equilibrium shifts. Students engage with interactive station-based task cards simulating real laboratory precipitates.

RBRaino Bhatti

Solubility Showdown

An AP Chemistry lesson exploring solubility rules, net ionic equations, particulate representations, and the mathematical link to Ksp and equilibrium shifts. Students engage with interactive station-based task cards simulating real laboratory precipitates.

RBRaino Bhatti

Cut along the dotted borders to place at lab stations

STATION 1

The Silver Screen

An AP chemistry student mixes \(25.0\,\text{mL}\) of \(0.20\,\text{M}\) silver nitrate, \(AgNO_3\), with \(25.0\,\text{mL}\) of \(0.20\,\text{M}\) sodium carbonate, \(Na_2CO_3\). A bright yellow-white precipitate forms rapidly.

• Write the complete balanced molecular equation.

• Write the net ionic equation representing the physical change.

• State which spectator ions remain unchanged in solution.

STATION 2

Lead Lactate Mystery

In the lab, you mix \(50.0\,\text{mL}\) of \(1.0 \times 10^{-4}\,\text{M}\ Pb(NO_3)_2\) with \(50.0\,\text{mL}\) of \(2.0 \times 10^{-3}\,\text{M}\ NaCl\) at \(25^\circ\text{C}\). Given that the \(K_{sp}\) of \(PbCl_2\) is \(1.7 \times 10^{-5}\):

• Calculate the diluted concentrations of both \(Pb^{2+}\) and \(Cl^-\) ions after mixing.

• Formulate the expression for the reaction quotient \(Q\).

• Determine if a precipitate of \(PbCl_2(s)\) will form at this equilibrium point.

STATION 3

Common Ion Crises

The solubility product constant (\(K_{sp}\)) for calcium sulfate, \(CaSO_4\), is \(2.4 \times 10^{-5}\) at room temperature.

• Calculate the molar solubility (\(s\)) of calcium sulfate in pure distilled water.

• Calculate the molar solubility of calcium sulfate in a \(0.10\,\text{M}\) sodium sulfate (\(Na_2SO_4\)) solution.

• Explain the physical reasoning behind this shift using Le Chatelier's Principle.

SOLUBILITY SHOWDOWN | PRINTABLE LAB CARDS (1-3) PAGE 3 OF 4

PRINTABLE LAB CARDS

Cut along the dotted borders to place at lab stations

STATION 4

Particulate Precision

Imagine mixing \(50.0\,\text{mL}\) of \(0.20\,\text{M}\) Iron(III) chloride, \(FeCl_3\), with \(50.0\,\text{mL}\) of \(0.30\,\text{M}\) sodium hydroxide, \(NaOH\). The Net Ionic reaction is: \(Fe^{3+}(aq) + 3\,OH^-(aq) \rightarrow Fe(OH)_3(s)\)

• Determine which reactant is fully consumed (the Limiting Reactant).

• Calculate the moles of remaining excess ions suspended in the final \(100\,\text{mL}\) solution.

• Translate this stoichiometry into a detailed particulate representation.

STATION 5

Barium Barrier (pH Dynamics)

The hydroxide salt Magnesium Hydroxide, \(Mg(OH)_2\), is sparingly soluble with a \(K_{sp} = 1.8 \times 10^{-11}\). Instead of pure water, you dissolve it in a robust buffer solution maintained at \(pH = 9.00\).

• Calculate the equilibrium concentration of \(OH^-\) enforced by the buffer.

• Calculate the new molar solubility (\(s\)) of \(Mg(OH)_2\) in this buffered environment.

• Explain why lowering the pH below 9 would increase the solubility of this solid.

STATION 6

Gravimetric Analysis Challenge

A solid alloy sample containing an unknown fraction of barium is analyzed. A \(1.50\,\text{g}\) alloy sample is dissolved, and excess sulfate solution is added to precipitate all barium as dry barium sulfate, \(BaSO_4\). You collect and dry \(0.466\,\text{g}\) of precipitate solid.

• Calculate the moles of barium sulfate precipitate collected.

• Find the mass of barium present in the original \(1.50\,\text{g}\) alloy sample.

• Determine the precise mass percent (\(\%\)) of barium in the original alloy.

SOLUBILITY SHOWDOWN | PRINTABLE LAB CARDS (4-6) PAGE 4 OF 4

• Spectator Ions (Unchanged):
\(Na^+(aq)\) and \(NO_3^-(aq)\)

STATION 2: Lead Lactate Mystery (\(Q\) vs. \(K_{sp}\)) Q vs Ksp Evaluation

The total mixed volume is \(V_t = 100.0\,\text{mL}\). Dilution math is required first:

• \([Pb^{2+}]_i = (1.0 \times 10^{-4}\,\text{M}) \times \frac{50.0\,\text{mL}}{100.0\,\text{mL}} = 5.0 \times 10^{-5}\,\text{M}\)

• \([Cl^-]_i = (2.0 \times 10^{-3}\,\text{M}) \times \frac{50.0\,\text{mL}}{100.0\,\text{mL}} = 1.0 \times 10^{-3}\,\text{M}\)

• Reaction Quotient:
\(Q = [Pb^{2+}][Cl^-]^2 = (5.0 \times 10^{-5})(1.0 \times 10^{-3})^2 = 5.0 \times 10^{-11}\)

• Conclusion: Since \(Q < K_{sp}\) (\(5.0 \times 10^{-11} < 1.7 \times 10^{-5}\)), the solution remains unsaturated. No precipitate of \(PbCl_2(s)\) forms.

STATION 3: Common Ion Crises (Equilibrium Shifts) Common Ion Effect

• Pure Water Molar Solubility (\(s\)):
\(K_{sp} = [Ca^{2+}][SO_4^{2-}] = s^2 \implies s = \sqrt{2.4 \times 10^{-5}} = 4.9 \times 10^{-3}\,\text{M}\)

• Solubility in \(0.10\,\text{M}\ Na_2SO_4\):
\(K_{sp} = [Ca^{2+}][SO_4^{2-}] = (s)(0.10 + s) \approx 0.10s\)
\(2.4 \times 10^{-5} = 0.10s \implies s = 2.4 \times 10^{-4}\,\text{M}\)

Le Chatelier explanation: The high initial \([SO_4^{2-}]\) shifts the equilibrium to the left, decreasing molar solubility by an order of magnitude.

SOLUBILITY SHOWDOWN | EXEMPLARY ANSWER KEY PAGE 2 OF 3

EXEMPLARY ANSWER KEY

STATIONS 4–6 SOLUTIONS

STATION 4: Particulate Precision (Drawing Guide) Stoichiometry

• Initial Moles: \(Fe^{3+} = 50\,\text{mL} \times 0.20\,\text{M} = 10.0\,\text{mmol}\); \(OH^- = 50\,\text{mL} \times 0.30\,\text{M} = 15.0\,\text{mmol}\).

• Reaction Stoichiometry: \(Fe^{3+} + 3\,OH^- \rightarrow Fe(OH)_3(s)\)

• Limiting Reactant: \(OH^-\) (runs out first). \(15.0\,\text{mmol}\ OH^-\) reacts with \(5.0\,\text{mmol}\ Fe^{3+}\).

• Remaining Excess Ions (in \(100\,\text{mL}\)):
\(Fe^{3+} = 5.0\,\text{mmol}\ (0.050\,\text{M})\), \(Cl^- = 30.0\,\text{mmol}\ (0.30\,\text{M})\), \(Na^+ = 15.0\,\text{mmol}\ (0.15\,\text{M})\).

Particulate Drawing Verification: The bottom solid should be alternating \(Fe^{3+}\) and \(OH^-\) ions (in a \(1:3\) ratio). Suspended randomly above must be separate \(Na^+\), \(Cl^-\), and excess \(Fe^{3+}\) ions.

STATION 5: Barium Barrier (pH-Driven Dissolution) pH Math

• \(pH = 9.00 \implies pOH = 5.00 \implies [OH^-] = 1.0 \times 10^{-5}\,\text{M}\)

• \(K_{sp} = [Mg^{2+}][OH^-]^2 \implies 1.8 \times 10^{-11} = (s)(1.0 \times 10^{-5})^2\)

• \(s = \frac{1.8 \times 10^{-11}}{1.0 \times 10^{-10}} = 0.18\,\text{M}\)

Solubility Contrast: In pure water, \(s = \sqrt[3]{K_{sp}/4} = 1.65 \times 10^{-4}\,\text{M}\). The low-pH buffer dramatically increases solubility because added acid depletes \(OH^-\) products, shifting equilibrium to the right.

STATION 6: Gravimetric Analysis Challenge Stoichiometry Steps

• \(Moles\ of\ BaSO_4 = \frac{0.466\,\text{g}}{233.38\,\text{g/mol}} = 2.00 \times 10^{-3}\,\text{mol}\)

• \(Moles\ of\ Ba^{2+} = Moles\ of\ BaSO_4 = 2.00 \times 10^{-3}\,\text{mol}\)

• \(Mass\ of\ Ba = 2.00 \times 10^{-3}\,\text{mol} \times 137.33\,\text{g/mol} = 0.275\,\text{g}\)

• \(Mass\ \%\ of\ Barium = \left(\frac{0.275\,\text{g}}{1.50\,\text{g}}\right) \times 100\% = 18.3\%\)

SOLUBILITY SHOWDOWN | EXEMPLARY ANSWER KEY PAGE 3 OF 3

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