chapter fifteen - ntut.edu.twchpro/chem/chap15.pdf · acid and corresponding conjugate base. added...
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Chapter Fifteen:
APPLICATIONS OF AQUEOUSEQUILIBRIA
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Contentsp680
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15-1 Solution of Acids or BasesContaining a Common Ion
p681
Le Chatelier’s Principle
Common ion effect
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The equilibrium concentration of OH- ionsis reduced by the common ion effect.
p682
The position of ammonia-waterequilibrium is shifted to the left.
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Ex 15.1 Acidic Solutions ContainingCommon Ions
p682
Calculate [H+] and the percent of HF in a solution
containing 1.0 M HF (Ka = 7.2 x 10-4) and 1.0 M NaF.
Solution:
1.0 M HF [H+] = 2.7 x 10 –2 M
The percent dissociation of 1.0 M HF is
2.7% ( 2.7 x 10-2/1.0)
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15-2 Buffered Solutionsp684
The most important application of acid-base solutions
containing a common ion is for buffering. A buffered
solution is one that resists a change in its pH when either
hydroxide ions pr protons are added. The most important
practical example of a buffered solution is our blood, which
can absorb the acids and bases produced in biologic reactions
without changing its pH. A constant pH for blood is vital
because cells can survive only in a very narrow pH range.
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Ex 15.2 The pH of a Buffered Solution I
Solution:
p684
The major species in the the solution are
HC2H3O2, Na+, C2H3O2-, and H2O
A buffered solution contains 0.50 M Acetic acid (HC2H3O2,
Ka = 1.8 x 10-5) and 0.050 M sodium acetate (NaC2H3O2).
Calculate the pH of this solution.
weak neither base very weakacid acid nor (conjugate baseor
base of HC2H3O2)base
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Solving Problems with Buffered Solutions
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Buffering: How Does It Work?p687
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Buffering: How Does It Work? p688
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Ex 15.4 The pH of a Buffered Solution II p689
Calculate the pH of a solution containing 0.75 M lacticacid (ka = 1.4 x 10-4) and 0.25 M sodium lactate. Lacticacid ) HC3H5O3) is a common constituent of biologicsystem. For example, it is found in milk and is presentin human muscle tissue during exertion.Solution:
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Buffers contain relatively large amounts of weakacid and corresponding conjugate base.
Added H+ reacts to completion with theconjugate base.
Added OH- reacts to completion with the weakacid.
The pH is determined by the ratio of theconcentrations of the weak acid and conjugatebase.
p692Summary of the Most ImportantCharacteristic of Buffered Solutions
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15-3 Buffering Capacityp693
The capacity of a buffered solution isdetermined by the magnitudes of [HA] and [A-]
Ex15.7 Adding strong Acid to a BufferedSolution II
Solution:
For A:
Initial:
For B:
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The optimal buffering system has a
pKa value close to the desired pH.
p696
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15-4 Titrations and pH Curves p696
Strong acid-Strong Base Titrations
A. No NaOH has been added.
[H+] = 0.200 M pH = 0.699
B. 10.0 mL of 0.100 M has been added.
H+(aq) + OH-
(aq) → H2O(l)
pH = - log(0.15) = 0.82
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17Na+, NO3-, H2O
C. 20.0 mL (total) of 0.100 M NaOH has been added.
pH = 0.942
D. 50.0 mL (total ) of 0.100 mL M NaOH has been added.
Preceding exactly as for points B and C, the pH is foundto be 1.301.
Enough OH- has been added to react exactly with H+
from the nitric acid. This is the stoichiometric point, orequivalence point, of the titration. At this point the majorspecies in solution are
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Titration p696
F. 150.0 mL (total) of 0.100 M NaOH has been added.
pH = 12.40
Proceeding as for point F,the pH is found to be 12.60
G. 200.0 mL (total) of0.100 M NaOH hasbeen added.
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Titration curve p699
Figure 15.1The pH curve for the titration of 50.0 mL of 0.200
M HNO3 with 0.100 M NaOH. Note that the equivalence
point occurs at 100.0 mL of NaOH added, the point where
exactly enough OH- has been added to react with all the H+
originally present. The pH of 7 at the equivalence point is
characteristic of a strong acid-base titration.
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Neutralization of a Strong Acid with a Strong Base
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The pH Curve for the Titration of 50.0 mL of0.200 M HNO3 with 0.100 M NaOH
p699
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Figure 15.2 The pH Curve for the Titrationof 100.0 mL of 0.50 M NaOH with 1.0 M HCI.
p699
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Figure 15.3 The pH Curve for the Titrationof 50.0 mL of 0.100 M HC2H3O2 with 0.100M NaOH.
Titrations of Weak Acids with Strong Basesp704
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The shapes of the strong and weak acid
curves are the same after the equivalence
points because excess OH- controls the pH in
this region in both cases.
p705
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Figure 15.4 The pH Curves for the Titrationsof 50.0-mL Samples of 0.10 M Acids withVarious Ka Values with 0.10 M NaOH.
The pH curves for the titrations ofsamples with various Ka
p707
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Weak Acid - Strong Base Titration
Step 1: A stoichiometry problem (reaction is
assumed to run to completion) then
determine remaining species.
Step 2: An equilibrium problem (determine
position of weak acid equilibrium and
calculate pH).
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Figure 15.5 The pH Curve for the Titrations of100.0mL of 0.050 M NH3 with 0.10 M HCl.
p711
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15-5 Acid-Base Indicators
Marks the end point of a titration by changing color.
The equivalence point is not necessarily the same
as the end point.
indicator
p711
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The acid and base forms of the indicatorphenolphthalein. The indicatorphenolphthalein is colorless in acidicsolution and pink in basic solution.
Figure 15.6
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Relative Solubilities
p721
CuI(s)
CaSO4(s)
16105.1 spK
12100.5 spK
5101.6 spK
AgI(s)
15.6 Solubility Equilibria andthe Solubility Product
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Common Ion Effect p722
Ex 15.15 Solubility and Common IonsCalculate the solubility of solid CaF2 (Ksp = 4.0 x 10-11) in a
0.025 M NaF solution.Solution:
Thus mol solid CaF2 dissolves per liter of the0.025 M NaF solution.
We will now see what happen the water containsan ion in common with the dissolving salt.
8104.6
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15-7 Precipitation and QualitativeAnalysis
p725
Ex 15.16 Determining Precipitation ConditionsA solution is prepares by adding 750.0 mL of 4.00 x 10-3
M Ce(NO3)3 to 300.0 mL of 2.00 x 10-2 M KIO3. Will
Ce(IO3)3 (Ksp = 1.9 x 10-10) precipitate from this solution?
Solution:
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Ex 15.18 Selective Precipitation p728
A solution contains 1.0 x 10-4 M Cu+ and 2.0 x 10-3 MPb2+. If a source of I- is added gradually to thissolution, will PbI2 (Ksp = 1.4 x 10-8) or CuI ( Ksp = 5.3 x10-12) precipitate first? Specify the concentration of I-necessary to begin precipitation of each salt.Solution:
As I- is added to the mixed solution, CuI willprecipitate first, since the [I-] required is less.
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15-8 Equilibria Involving Complex Ions
]][NH)[Ag(NH])[Ag(NH
102.833
2332
K
mL)(200.0)mL)(2.0(100.0
][NH 03M
p731
Ag+ + 2NH3 → Ag(NH3)2+
Before reaction: 5.0 x 10-4 M 1.0 M 0 M
After reaction: 0 1.0-2(5.0 x 10-4) = 1.0 M 5.0 x 10-4 M
mL)(200.0)10mL)(1.0(100.0
][Ag3
0M
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Complex Ion Equilibria p731
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Nickel(II) Complexes
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Ex 15.19 Complex Ions
8132
232 104.7)OAg(SOSAg K
Calculate the concentrations of Ag+, Ag(S2O3)-, and
Ag(S2O3)3- in a solution prepared by mixing 150.0 mL of
1.00 x 10-3 M AgNO3 with 200.0 mL of 5.00 M Na2S2O3.
The stepwise formation equilibria are:
42
3232
23232 109.3)OAg(SOS)OAg(S K
p733
Solution:
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p733
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Complex Ions and Solubility p734
The solubility in pure water is
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Separation Scheme