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Question: Standard electrode potentials of \(F{e^{2 + }} + 2{e^ - } \to Fe\) and \(F{e^{3 + }} + 3{e^ - } \to ...

Standard electrode potentials of Fe2++2e−→FeF{e^{2 + }} + 2{e^ - } \to Fe and Fe3++3e−→FeF{e^{3 + }} + 3{e^ - } \to Fe are−0.440V - 0.440V and −0.036V - 0.036V respectively. The standard electrode potential (E∘)({E^ \circ }) for Fe3++e−→Fe2+F{e^{3 + }} + {e^ - } \to F{e^{2 + }} is:
A.−0.476V - 0.476V
B.−0.404V - 0.404V
C.+0.404V + 0.404V
D.+0.772V + 0.772V

Explanation

Solution

Ecell{E_{cell}} of a reaction is defined as electrode potential of the cell and E∘cell{E^ \circ }_{cell} of a reaction is defined as electrode potential measured at 11 atmosphere pressure, 11 molar solution at 25∘C{25^ \circ }C also known as standard electrode potential.

Complete step by step solution:
First of all let us talk about how to find E∘cell{E^ \circ }_{cell} of the reaction when you know the values of E∘{E^ \circ } of its components i.e. the ions or atoms which are reduced or oxidised in the reaction.
Reduced ions or atoms are that in which there is decrease in the positive charge on the ion i.e. gain of electrons.
Oxidised ions or atoms are those in which there is an increase in the positive charge on the ion i.e. loss of electrons.
Reaction given is as:
Fe3++e−→Fe2+F{e^{3 + }} + {e^ - } \to F{e^{2 + }}
Therefore the reaction at anode will be: Fe→Fe2++2e−Fe \to F{e^{2 + }} + 2{e^ - } and also we know the value of the E∘{E^{^ \circ }} of the reverse reaction i.e. Fe2++2e−→FeF{e^{2 + }} + 2{e^ - } \to Fe as −0.440V - 0.440V. So the E∘{E^{^ \circ }} of the this reaction i.e. Fe→Fe2++2e−Fe \to F{e^{2 + }} + 2{e^ - } will be 0.440V0.440V.
The reaction at cathode will be as: Fe3++3e−→FeF{e^{3 + }} + 3{e^ - } \to Fe and also we know the value of E∘{E^ \circ } as −0.036V - 0.036V.
Now if in the reaction we know which is oxidised and which is a reduced element and we also know the values of E∘{E^ \circ } of its components i.e. the ions or atoms. Then we can calculate the value of E∘cell{E^ \circ }_{cell} of the reaction as:   E∘cell=  E∘R+  E∘L\;{E^ \circ }_{cell} = \;{E^ \circ }_R + \;{E^ \circ }_L (because already we reverse the reverse at anode) where E∘R{E^ \circ }_R is the E∘{E^ \circ }of the atom which is at right side (cathode) and E∘L{E^ \circ }_L is the E∘{E^ \circ } of the atom which is at left side (anode).
Hence E∘=−0.036+(0.440)=0.404V{E^ \circ } = - 0.036 + (0.440) = 0.404V.

So, option (C) is Correct.

Note: The relation between E∘cell{E^ \circ }_{cell} and equilibrium constant i.e. Keq{K_{eq}}. The relation is as:
E∘=0.059nlog⁡Keq{E^ \circ } = \dfrac{{0.059}}{n}\log {K_{eq}} where E∘cell{E^ \circ }_{cell} is cell voltage, Keq{K_{eq}} is equilibrium constant and nn is total number of electrons transfer in the reaction.