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I. Materials
Quantity Material
4pcs Beaker
Metal
CuSO4 solution
Zn(NO3)2 solution
1 pc. Multimeter
Deionized water
II. Methodology
Four small (~50 mL) beakers were obtained and filled with three-fourths
full of the 0.1 M solutions. Strips of copper, zinc, magnesium, and iron metal
were polished with steel wool, rinsed with dilute (~0.1 M) HNO3, and was rinsed
with deionized water. The polished metals, used as electrodes, were bent to
(electrode) in the Zn(NO3)2 solution. A piece of filter paper was rolled and
flattened; the filter paper was damped with a 0.1 M KNO3 solution. The ends of
the filter paper were folded and inserted into the solutions in the two beakers; this
served as the salt bridge. The multimeter was set to the 2000-mV range. One
electrode was connected to the negative terminal of the multimeter and the other
The connections to the electrodes were reversed when the multimeter read
a negative potential. The (positive) cell potential were read and recorded. The
metal strips that serve as the cathode (positive terminal) and the anode were
written and the two half-reactions were combined to write the equation for the cell
reaction.
The cell potentials were determined for all possible galvanic cells that can
be constructed from the four redox couples. A new salt bridge was prepared for
0.79 V, and the reduction potentials of all other redox couples were calculated.
A 0.1 M solution together with the electrode obtained from the instructor
was placed in a small beaker. The reduction potential, relative to the Zn2+(0.1
M)/Zn redox couple was determined for the unknown redox couple.
The galvanic cell was set up using 1 M CuSO4 and 0.001 M CuSO4
bridge was prepared to connect the two half-cells. The cell potential was
measured. The anode and the cathode were also determined. Lastly, an equation
2–5 mL of 6 M NH3 was added to the 0.001 M CuSO4 solution until any
precipitate redissolves. Changes in the half-cell and the cell potential were
2–5 mL of 0.2 M Na2S was added to the 0.001 M CuSO4 solution that
contains the added NH3. What happened to the cell potential and half-cell were
flasks. The pipet was rinsed with more concentrated solution before making the
transfer. Deionized water was used for the dilution to the mark in the volumetric
flasks. The molar concentration of the Cu2+ ion was calculated for each solution
The experiment was set up using small (~50 mL) beakers. The reference
half-cell for this part of the experiment was the Zn2+/Zn redox couple. The two
half-cells were connected with a new salt bridge. The multimeter was reset to the
lowest range (~200 mV). The electrodes were connected to the multimeter and the
potential difference, Ecell, expt was recorded. The theoretical cell potential Ecell, calc.
(Using a table of standard reduction potentials and the Nernst equation) was
calculated.
Part C.2 with solutions 3 and 2 were repeated respectively. For each cell, a
Ecell, expt and Ecell, calc (ordinate) were plotted versus pCu (abscissa) by using
concentration from the instructor and was set up like a galvanic cell. Ecell was
determined as in Part C.2. The unknown copper(II) ion concentration in the