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In this experiment you will study the
heterogeneous equilibrium of a slightly soluble
salt and its ions in aqueous solution. The
solubility product constant will be determined for
copper(II) iodate for several different
concentrations of Cu2+ and
IO3-. The equilibrium is:
Cu(IO3)2(s)
<--> Cu2+ +
2IO3-
and the equilibrium constant expression is:
Ksp -=
[Cu2+][IO3-]
To find the numerical value of Ksp,
it is necessary to know the concentrations of both
Cu2+ and IO3- at
equilibrium. The concentration of Cu2+
may be easily determined spectrophotometrically by
comparing the absorbance of the unknown to that of
a standard. In this experiment the concentrations
of Cu2+ are too low to produce a
sufficiently high absorbance; therefore, the color
is intensified by adding NH3(aq) to form
the deep blue ion,
Cu(NH3)42+. The
concentrations of IO3- are
determined indirectly by knowing that the change
from the initial concentration to the equilibrium
concentration will be twice that of the
Cu2+.
Procedure
Clean and dry with a paper towel four 15-cm test
tubes. Clean and drain (but do NOT dry) two Spec 20
cuvets. Clean a 25 mL buret and rinse it with two
2-mL portions of 0.150 M CuSO4 solution.
Fill the buret with 0.150 M CuSO4 and
deliver the volumes as described below into the
appropriate test tubes. Also add 2.00 mL of the
CuSO4 solution to a clean and drained
25-mL graduated cylinder. Add enough water to bring
the level up to 25.0 mL. Stir this solution to make
it homogenous. Clean the buret and rinse it with
two 2-mL portions of 0.320 M HIO3
solution. Fill the buret with 0.320 M
HIO3 and deliver the volume as indicated
below into the appropriate test tube.
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Test Tube Number
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1
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2
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3
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4
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mL of 0.150 M CuSO4
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5.40
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5.70
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6.00
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6.30
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mL of 0.320 M HIO3
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6.60
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6.30
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6.00
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5.70
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Stir with a stirring rod the solution in test tube 1
until precipitation begins (about 2 minutes). Remove the
rod, rinse and dry it, and stir test tube 2 until a
precipitate forms. Repeat for test tubes 3 and 4. After
precipitation has started, shake the solutions frequently
for at least 20 minutes.
Filter the solution in test tube 1 into a labeled clean
and dry small beaker. Do not wet the filter paper before
titration! (Why?) Rinse and dry the funnel and with new
filter paper filter the solution of test tube 2 into another
clean and dry beaker. Continue for test tubes 3 and 4. To a
fifth clean and dry beaker, add the same volume of standard
Cu2+ ion solution from your graduated cylinder as
in each of the other four beakers. In the hood, add 15 drops
of concentrated ammonia solution to each of the beakers and
mix well.
Rinse a Spec 20 cuvet with a small portion of the
filtrate in beaker 1. Fill the cuvet about half-way with
filtrate 1. Measure the absorbance at 603 nm using deionized
water in the other cuvet as a blank. Rinse the sample cuvet
with deionized water and then with a small portion of the
filtrate in beaker 2. Fill the cuvet to the same level as
before and measure its absorbance. Repeat for solutions 3,
4, and the standards.
Assuming that Beer's Law is valid, the unknown
concentrations of Cu2+ in the four beakers may be
calculated using:
[Cx] = [Cstd]
Ax/Astd = [Cu2+]
where Cstd is the calculated concentration of
the standard Cu2+ solution.
Results
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Solution number
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number 1
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number 2
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number 3
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number 4
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number 5 (standard)
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Measured Absorbance
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Measured % T
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Calculated Absorbance (-log T)
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Concentration of Cu2+ in 12 mL
mixture before ppt. (calculated)
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After ppt.
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Decrease in Cu2+ concentration
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Decrease in IO3-
concentration
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Concentration of IO3- in
12 mL mixture before ppt. (calculated)
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After ppt.
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Solubility product
[Cu2+][IO3-]2
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DDM/MLK/DSR:clm 12/83
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