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Irene Metz
General Chemistry II
9 April 2020
Beginning Questions:
3. Initial predictions included: The original prediction for this lab was that a higher
Safety Considerations: With only a computer in use, few safety considerations need to be
administered in this lab. However, caution with the electronics and liquids that could harm the
● To begin this lab, the Galvanic Cells simulation was launched in a web browser
● A reference image of the simulation is shown here:
● Using the tabs on the right of the simulation, a total of ten different cells were built using
○ Two different metal solutions were chosen, taking note of the concentrations
○ The solutions were transferred to separate dishes in the apparatus in the center of
the simulation
○ A strip of metal with the same identity as one of the electrodes was placed into its
corresponding solution
○ Using the paper strips selection in the bottom right, a salt bridge was formed on
the central apparatus by placing the strips to connect the two electrodes through
○ The voltage of the cell was recorded as shown in the top right (if the voltage
appeared negative, the placement of the red and black clips were switched)
● Once ten tests had been performed in the simulation, Google Sheets was utilized to
compile results, check the % error of the program using the Nernst equation and literature
values found in the textbook, and answer any further Data Analysis questions
Calculations:
Nernst
Cath Electri Equati
Anode ode c on % Gibbs Free Gibbs Free
Anode Cathode Soluti Soluti Half Potenti Value Erro Energy Energy
(Black) (Red) on on Reactions Full Reaction al (V) (V) r (Simulation) (Literature) % Error
1M 1M Zn(s) --> Zn(s) + 2Ag+
ZnSO AgN Zn2+(aq) + (aq) --> Zn2+
1 Zn Ag+ 4 O3 2e- (aq) + 2Ag(s) 1.56 1.56 0 -301080 -301080 0
Ag+(aq) +
e- --> Ag(s)
3.74
0.1 M 1 M Zn(s) --> Zn(s) + 2Ag+ 937
ZnSO AgN Zn2+(aq) + (aq) --> Zn2+ 1.589 091
2 Zn Ag+ 4 O3 2e- (aq) + 2Ag(s) 1.53 6 1 -295290 -306792.8 3.749370911
Ag+(aq) +
e- --> Ag(s)
3 Zn Ag+ 0.1 M 0.01 Zn(s) --> Zn(s) + 2Ag+ 1.59 1.530 3.89 -306870 -295367.2 3.894406691
ZnSO M Zn2+(aq) + (aq) --> Zn2+ 4 440
4 AgN 2e- (aq) + 2Ag(s) 669
O3
1
Ag+(aq) +
e- --> Ag(s)
0.001 7.94
0.1 M M Zn(s) --> Zn(s) + 2Ag+ 243
ZnSO AgN Zn2+(aq) + (aq) --> Zn2+ 1.500 070
4 Zn Ag+ 4 O3 2e- (aq) + 2Ag(s) 1.62 8 4 -312660 -289654.4 7.942430704
Ag+(aq) +
e- --> Ag(s)
0.001 0.001
M M Zn(s) --> Zn(s) + 2Ag+
ZnSO AgN Zn2+(aq) + (aq) --> Zn2+
5 Zn Ag+ 4 O3 2e- (aq) + 2Ag(s) 1.56 1.56 0 -301080 -301080 0
Ag+(aq) +
e- --> Ag(s)
1 M Sn(s) --> Sn(s) + Cu2+
1M Cu(N Sn2+(aq) + (aq) --> Sn2+
6 Sn Cu2+ SnCl2 O3)2 2e- (aq) + Cu(s) 0.48 0.48 0 -92640 -92640 0
Cu2+(aq) +
2e- -->
Cu(s)
Mg(s) +
1M 1M Mg(s) --> 2Ag+(aq) -->
Mg(N AgN Mg2+(aq) + Mg2+(aq) +
7 Mg Ag+ O3)2 O3 2e- 2Ag(s) 3.17 3.17 0 -611810 -611810 0
Ag+(aq) +
e- --> Ag(s)
1M 1 M Zn(s) --> Zn(s) + Sn2+
ZnSO SnCl Zn2+(aq) + (aq) --> Zn2+
8 Zn Sn2+ 4 2 2e- (aq) + Sn(s) 0.62 0.62 0 -119660 -119660 0
Sn2+(aq) +
2e- -->
Sn(s)
0.000 47.5
1M 1 M Zn(s) --> Zn(s) + 2Ag+ 279
ZnSO SnCl Zn2+(aq) + (aq) --> Zn2+ 0.501 106
9 Zn Sn2+ 4 2 2e- (aq) + 2Ag(s) 0.74 6 9 -142820 -96808.8 47.52791069
Ag+(aq) +
e- --> Ag(s)
0.000 33.6
0.1 M 1 M Zn(s) --> Zn(s) + 2Ag+ 596
ZnSO SnCl Zn2+(aq) + (aq) --> Zn2+ 0.531 385
10 Zn Sn2+ 4 2 2e- (aq) + 2Ag(s) 0.71 2 5 -137030 -102521.6 33.65963855
Ag+(aq) +
e- --> Ag(s)
● Class Data
● Formulas
Claims: With the simulation complete and data gathered, we can now claim to answer our
beginning questions. The electric potential difference for a cell composed of 1 M ZnSO4 & 1 M
AgNO3 solutions is 1.56 volts. A relationship between electrode concentration and Gibbs Free
Energy exists: greater differences between solution concentrations create a larger change in
Gibbs Free Energy, & when the anode possesses the higher solution concentration, the voltage
drops, and the inverse occurs when the cathode possesses the larger concentration.
Evidence and Analysis: The evidence for the above claims comes from the data personally
gathered from this simulation as well the other data & calculations performed by classmates. The
simulation provided the evidence for the tested reaction between zinc and silver. The evidence
for the relationship between Gibbs Free Energy and concentration was based upon values
calculated from the Nernst Equation. Due to issues discussed in the error analysis, the calculated
values were used for these claims instead of directly referencing the listed voltages from the
simulation. Analyzing the reactions between two of the electrodes, Zn and Ag, a pattern exists
against the standard 1:1 M voltage of 1.56 V. When the anode zinc’s concentration is lowered to
1/10th of silver’s, the voltage increases by 0.03. Likewise, when the concentrations are zinc 0.1
M and silver 0.01 M, the voltage drops by 0.03 from the 1.56 V standard. This behavior is
rigorous within the context of the Nernst equation that is used to calculate it: when the reaction
quotient Q is greater than 1, the log(Q) is greater than 0, thus increasing the Ecell from the
standard voltage. Likewise, when Q < 1, the log(Q) is negative, decreasing the voltage. The
value of Q is determing by the concentrations of products over reactants, or, in this case,
anode/cathode. Thus, an anode:cathode ratio > 1 produces a positive log(Q), raising the voltage,
a. Error Analysis: The most important point of error in this simulation occurred with the
other class data calculations, the simulation’s voltage readings for cells of equivalent
concentrations had 0% error from the calculated values. However, any calculations that
were made with solutions of differing concentrations were inaccurate from the actual
calculated value using the Nernst equation. Some errors were small--less than 10%--but
some voltage readings saw percent errors near 50%. This is a critical error because the
voltage readings given by the simulation are in direct contradiction to this report’s claims
on the relationship between free energy and concentration, indicating the reverse.
b. Changed Ideas, New Questions: Looking at my original predictions, I would say that
my notion on the impact concentration has on ΔG was different from what this simulation
indicates. I was under the assumption more ions in the solution would lead to more
reactions, thus a higher voltage. However, this simulation’s finding, that greater
differences in concentration impact the magnitude of ΔG, does make sense when put into
the context of the Nernst equation. Since the Nernst equation was the cornerstone formula
for the evidence and analysis of this lab, I would like to repeat this lab with a simulation
that does not have as many apparent issues with handling the equations. If this simulation
worked correctly, all calculations made by hand or in Microsoft Excel should have a
over electrochemistry and voltaic cells. Outside of the lab, the uses of batteries, cells, and
electricity is incredibly hard to miss. Batteries are utilized to power devices such as cell
phones, tablets, or even the computer this simulation was run on. On a wider scale,
scientists and engineers are also looking to electrochemistry to develop new types of