I forgot to include that the above problem is accompanied with a virtual lab that would help determine E.
However, I don't know how to predict the value of E based on the virtual lab.
PS: I don't know how to post a link on this forum and so in order to visit the virtual lab website, follow these directions:
1. Type in "Chem collective" in the search bar
2. Click on the very first website
3. At the Resources by topic side bar, click on Oxidation/Reduction and Electrochemistry
4. Under the Galvanic Cell tab, click on Electrochemistry: Galvanic Cells and the Nernst Equation
5. At the left side bar under step 4, click on Practice with nonstandard cells
Using the Nernst equation, determine the diluted concentration for both cells. Show your work.
Sn| Sn2+(diluted)||Cu2+|Cu
Zn| Zn2+ ||Sn2+(diluted)|Sn
2 answers
If you can figure out the non-standard cell potentials for your problem, then substitute in the Nernst Equations at the end of this dialog...
For [Zn⁰(s)│Zn⁺²(aq)ǁSn⁺²(aq)│Sn⁰(s)]
Half-Cell 1 => Zn⁰(s) => Zn⁺²(aq) +2e¯; E⁰ = - 0.0.76v (oxidation half-rxn)
Half-Cell 2 => Sn⁺²(aq)+ 2e¯ => Sn⁰(s); E⁰ = - 0.14v (reduction half-rxn)
Standard Cell Potential E⁰(Zn/Sn) = E⁰(Sn) - E⁰(Zn) = (-0.14v) – (-0.76v) = 0.62v
E = E⁰ - (0.0592/n)log([Oxid’n Cation]/[Red’n Cation])
E = Non-Standard Cell Potential
E⁰ = Standard Cell Potentials = E⁰(Reduction) - E⁰(Oxidation)
n = electron transfer in balanced oxidation-reduction reactions
Given: [Cu⁺²] and [Zn⁺²] are both 2M
Case I (Sn/Cu) Cell:
E(Sn/Cu) = E⁰(Sn/Cu) – (0.0592/n)logQ(c)
E(Sn/Cu) = E⁰(Sn/Cu) – (0.0592/n)logQ([Sn⁺²]/[Cu⁺²])
E(Sn/Cu) = (0.62v) – (0.0592/n)log([Sn⁺²]/[2.0M])
Case II (Zn/Sn) Cell:
E(Zn/Sn) = E⁰(Zn/Sn) – (0.0592/n)logQ(c)
E(Sn/Cu) = E⁰(Zn/Sn) – (0.0592/n)log([Zn⁺²]/[Sn⁺²])
E(Sn/Cu) = (0.62v) – (0.0592/n)log([2.0M]/[Zn⁺²])
For [Zn⁰(s)│Zn⁺²(aq)ǁSn⁺²(aq)│Sn⁰(s)]
Half-Cell 1 => Zn⁰(s) => Zn⁺²(aq) +2e¯; E⁰ = - 0.0.76v (oxidation half-rxn)
Half-Cell 2 => Sn⁺²(aq)+ 2e¯ => Sn⁰(s); E⁰ = - 0.14v (reduction half-rxn)
Standard Cell Potential E⁰(Zn/Sn) = E⁰(Sn) - E⁰(Zn) = (-0.14v) – (-0.76v) = 0.62v
E = E⁰ - (0.0592/n)log([Oxid’n Cation]/[Red’n Cation])
E = Non-Standard Cell Potential
E⁰ = Standard Cell Potentials = E⁰(Reduction) - E⁰(Oxidation)
n = electron transfer in balanced oxidation-reduction reactions
Given: [Cu⁺²] and [Zn⁺²] are both 2M
Case I (Sn/Cu) Cell:
E(Sn/Cu) = E⁰(Sn/Cu) – (0.0592/n)logQ(c)
E(Sn/Cu) = E⁰(Sn/Cu) – (0.0592/n)logQ([Sn⁺²]/[Cu⁺²])
E(Sn/Cu) = (0.62v) – (0.0592/n)log([Sn⁺²]/[2.0M])
Case II (Zn/Sn) Cell:
E(Zn/Sn) = E⁰(Zn/Sn) – (0.0592/n)logQ(c)
E(Sn/Cu) = E⁰(Zn/Sn) – (0.0592/n)log([Zn⁺²]/[Sn⁺²])
E(Sn/Cu) = (0.62v) – (0.0592/n)log([2.0M]/[Zn⁺²])