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Solubility Product Constant, Ksp
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Solubility is the maximum amount of solute in a solvent at a given temperature saturated solution, [ ]max equilibrium between: solid crystals dissolved ions eg. AgNO3(s) Ag1+(aq) NO31-(aq)
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1st 1st - H2O needs to separate - H-bonding needs to be overcome
- dissolving - NRG input
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3rd 2nd 3rd 2nd - H2O removes ions from the lattice - dissociation
- NRG input 2nd 3rd - hydration of ions - Ion – dipole force 3rd - NRG output - with H2O
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• solubility is a contest between:
• ionic bond strengths vs ion-dipole forces • lattice energies vs hydration energies • usually exothermic with increased disorder • if undissolved solid is present, then it is a mixture with a saturated sol’n phase
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Solubility Product Constant, Ksp:
equilibrium expression for slightly soluble salts If: AxBy(s) xAm+(aq) yBn-(aq) Then:
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Saturation can be tested by Q:
If: Q = Ksp then it is a saturated solution Q > Ksp there is noticeable precipitate Q < Ksp unsaturated Terminology: refers to the amount of solid that can dissolve not how much is in solution solubility units are g/100g or g/100 mL or g/L
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To find molar solubility from solubility:
(concentration) [ ]max = solubility ÷ Msolute x V adjustment or 1/ Msolute eg. Solubility of Mg(OH)2 is 3.45 g/100 mL.
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To find solubility from molar solubility:
(concentration) Solubility = molar solubility x Msolute x V adjustment eg. Molar solubility of Mg(OH)2 is mol/L. Do not divide by 100 mL
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1st - calculate the [ ] from solubility:
1) Ksp from solubility eg. Calculate the Ksp of Ag2CO3 given its solubility of g/100g. 1st - calculate the [ ] from solubility: 2nd - create ICE table. - Since dealing with a solid, the equilibrium is simplified
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Ag2CO3 ↔ 2 Ag+ + CO32- ; Q – not necessary 100 Rule – not necessary
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2) Solubility from Ksp types: solubility, molar solubility, [ion]eq, amount of solid that will dissolve - all from calculating “x” eg. How much PbI2 at SATP will dissolve in 1.00 L of water? Give the solute ion concentration, [Pb2+]eq, solubility (g/100mL) and molar solubility. - when not given the Ksp and not asked to calculate it, find it in the reference table or the textbook Ksp of PbI2 from textbook is 8.5 x 10-9
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PbI2 ↔ Pb2+ + 2 I1- ; ICE +x +2x = the molar solubility
- as the solid is not included and the [ion]i = 0, we can write ICE horizontally instead of vertically PbI2 ↔ Pb I1- ; ICE +x x = the molar solubility
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Predicting Precipitation:
Don’t by it is a unit 100 mL Predicting Precipitation: • Used to determine precipitation when mixing 2 sol’ns just like in double displacement rxns
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eg. Will precipitation occur when 5. 0 ml of 0
eg. Will precipitation occur when 5.0 ml of M AgNO3 is mixed with 1.0 ml of M Na2CrO4? (Ksp = 1.1 x for Ag2CrO4)? 1st – write down each reaction and calculate the V and C values
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3rd – calculate Q and compare with Ksp
2nd – write down the equilibrium equation, calculate the new [ ] in the combined sol’n Ag2CrO4 ↔ 2 Ag CrO42- ; 3rd – calculate Q and compare with Ksp
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eg. Will 0. 10 mg of Ba(OH)2 added to 75 mL of 2
eg. Will 0.10 mg of Ba(OH)2 added to 75 mL of 2.0 x 10-3 M AgNO3 solution form a precipitate? (Ksp (AgOH) = 1.5 x 10-17)? Ba(OH)2 Ba OH- = 1.17 x 10-6 mol C = 2.0 x 10-3 M V = L
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AgOH ↔ Ag+ + 2 OH- ; C = 2.0 x 10-3 M = 1.56 x 10-5 M
Ksp = [Ag+][OH-] = 1.5 x 10-17 C = 2.0 x 10-3 M = x 10-5 M Q = (2.0 x 10-3)(1.56 x 10-5) = 3.1 x 10-8 M Q (3.1 x 10-8) > Ksp (1.5 x 10-17)
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