In: Chemistry
I am asked to create a table of reducing potentials by setting ANY of the half-cell potential to 0V. Show calculations.
My half-cells and their Eocell is :
Ag+ + e- = Ag(s) 0.80V
Cu2+ + 2e- = Cu(s) 0.34V
Pb2+ + 2e- = Pb(s) -0.13V
Sn2+ + 2e- = Sn(s) -0.14V
Fe2+ + 2e- = Fe(s) -0.44V
Zn2+ + 2e- = Zn(s) -0.76V
Mg2+ + 2e- = Mg(s) -2.37V
Universally, hydrogen has been recognized as having reduction and oxidation potentials of zero. Therefore, when the standard reduction and oxidation potential of chemical species are measured, it is actually the difference in the potential from hydrogen.
so the half cell potential is actually the differenct from the zero cell potential.
suppose we assume the reduction cell potential of the below reaction to be zero
Sn2+ + 2e- Sn(s) actual potential = -0.14 V, we assume it to be zero than for any other reaction let's say for
Pb2+ + 2e- Pb (s) actual potential = -0.13 V but
potential difference from Sn = (-0.13 V) - (-0.14 V) = 0.01 V
similarly for
Zn2+ + 2e- Zn(s)
potential difference from Sn= (-0.76 V)- (-0.14 V) = -0.62 V
similarly we can calculate potential difference for all of the reactions and arranage them in order
Note:- i have assume the potential of Sn2+ + 2e- Sn(s) to be zero, you can assume for any other reaction and calculate the difference as mentioned above
Ag+ + e- Ag(s) 0.94 V
Cu2+ + 2e- Cu(s) 0.48 V
Pb2+ + 2e- Pb (s) 0.01 V
Sn2+ + 2e- Sn(s) 0 V
Fe2+ + 2e- Fe(s) -0.30 V
Zn2+ + 2e- Zn(s) -0.62 V
Mg2+ + 2e- Mg(s) - 2.59 V