The first thing to do is to calculate the emf of the cell under standard conditions.
We can do this using standard electrode potentials (sf(E^@)):
List the 1/2 equations in order least positive to most positive:
" " "E"^@("V")
stackrel(color(white)(xxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxx))(color(blue)(larr)
sf(Sn^(4+)" "+" "2e" "rightleftharpoons" "Sn^(2+)" "+0.15)
sf(Au^(3+)" "+" "3e" "rightleftharpoons" "Au" "+1.52)
stackrel(color(white)(xxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxx))(color(red)(rarr)
The more +ve half - cell will take in the electrons so the reactions in each half - cell will proceed in the direction shown by the arrows.
This gives the overall cell reaction:
sf(2Au^(3+)+3Sn^(2+)rarr2Au+3Sn^(4+))
To find sf(E_(cell)^@) subtract the least +ve electrode potential from the most positive:
sf(E_(cell)^@=+1.52-(+0.15)=1.37color(white)(x)V)
Since we are not under standard conditions we now need to use The Nernst Equation.
A useful form of this at sf(25^@C) is:
sf(E_(cell)=E_(cell)^@-(0.05916)/(z)logQ)
sf(z) is the number of moles of electrons transferred which, in this case = 6.
sf(Q) is the reaction quotient and is given by:
sf(Q=([Sn^(4+)]^(3))/([Au^(3+)]^(2)[Sn^(2+)]^(3))
:.sf(Q=((0.5)^(2))/((1.45)^(2)xx(0.87)^(3))=0.0902color(white)(x)"mol"^(-2).l^(2))
:.sf(E_(cell)=1.37-(0.05916)/(6)log[0.0902])
sf(E_(cell)=1.37+0.103=+1.38color(white)(x)V)