I just wanted to double-check something.
1. When a question tells you that a redox equation is predicted to occur based on the electrochemical series, but doesn't in reality, the reason has to do with reaction rate, NOT with non-standard conditions.
2. When a question tells you that a galvanic cell is predicted to result in a particular voltage, but the voltage is lower in reality, the reason has to do with non-standard conditions, NOT with reaction rate.
Are there any other reasons? Also, when is 'side reactions occur' a viable answer?
Thanks.
Generally, non-standard conditions don't affect the ordering too much. Look up "Nernst equation" for more details.
E
cell=E
ocell+RT*ln(Q)/nF
E
cell is the electrode potential difference
E
ocell is the standard potential difference, found by reading off the electrochemical series
where n is the number of electrons transferred per reaction, Q is the reaction quotient/concentration fraction, using pressures of gases in bars (100 kPa), concentrations in M and assigning values of pure liquids and solids of 1; F is 96500 C/mol, Faraday's constant, and R is the ideal gas constant.
If we have T=298 K, then the large number of symbols becomes 0.0257*ln(Q)/n
As you can see, Q has to increase incredibly for the actual cell potential to change by much.
To be honest, I still don't quite get though why at 5 M, the oxidation of chloride is preferred...this equation says that the reduction potential of chloride ion at 5 M relative to SHE would only increase to 1.25 V, still lower than that of water. I'm presuming that when saturated, activity coefficients are no longer close to one, so the activities in the reaction quotient may no longer be directly replaced with concentrations...