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Calculations At equivalence point, moles acid = moles base Initial pH = pH of a weak acid solution (ICE chart) pH before equivalence point – Buffer Calculation pH at equivalence point – pH of a weak base solution (ICE chart) pH after equivalence point
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For a strong acid-strong base titration, the pH begins at less than 7 and gradually increases as base is added. Near the equivalence point, the pH increases dramatically. For a weak acid-strong base titration, the initial pH rise is more steep than the strong acid-strong base case. However, then there is a leveling off due to buffer effects.
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pH at Equivalence Point
Type of Titration pH at Equivalence Point Strong Acid and Strong Base 7 Strong Acid and Weak Base <7 Strong Base and Weak Acid >7 Weak Base and Weak Acid If Ka>Kb, pH<7 If Ka<Kb, pH>7
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Titrations of Polyprotic Acids
In polyprotic acids, each ionizable proton dissociates in steps. Therefore, in a titration there are n equivalence points corresponding to each ionizable proton. In the titration of H3PO3 with NaOH. The first proton dissociates to form H2PO3-. Then the second proton dissociates to form HPO32-.
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Diprotic acids titration curve looks like…
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A picture is worth a 2 point bonus
Diprotic acids titration curve looks like… A picture is worth a 2 point bonus 2nd equivalence point 1st equivalence point pH of weak acid
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Solubility and Ksp To convert solubility to Ksp solubility needs to be converted into molar solubility (via molar mass); molar solubility is converted into the molar concentration of ions at equilibrium (equilibrium calculation), Ksp is the product of equilibrium concentration of ions.
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Factors that Affect Solubility
The Common Ion Effect Solubility is decreased when a common ion is added. This is an application of Le Châtelier’s principle: as F- (from NaF, say) is added, the equilibrium shifts away from the increase. Therefore, CaF2(s) is formed and precipitation occurs. As NaF is added to the system, the solubility of CaF2 decreases.
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Again we apply Le Châtelier’s principle:
Solubility and pH Again we apply Le Châtelier’s principle: If the F- is removed, then the equilibrium shifts towards the decrease and CaF2 dissolves. F- can be removed by adding a strong acid: As pH decreases, [H+] increases and solubility increases. The effect of pH on solubility is dramatic. Acidic salts are more soluble in basic solution and less soluble in acidic solution Basic salts are more soluble in acidic solution and less soluble in basic solution.
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Formation of Complex Ions
Consider the formation of Ag(NH3)2+: The Ag(NH3)2+ is called a complex ion. NH3 (the attached Lewis base) is called a ligand.
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