Equilibrium Potential of Half Cell

In summary, the equilibrium potential of half cell is the potential difference between the anode and cathode when the cell is at equilibrium. It is calculated using the Nernst equation and can be affected by temperature, ion concentration, and electrode and ion nature. This potential is important in electrochemistry as it determines the direction and magnitude of electron flow and influences the overall cell potential. The equilibrium potential differs from the standard cell potential as it only considers the potential difference within one half cell, while the standard cell potential takes into account the transfer of electrons between two half cells.
  • #1
garbagefish
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Homework Statement


Given the following half-reactions:
Ce4+ + e− → Ce3+ E° = 1.72 V
Fe3+ + e− → Fe2+ E° = 0.771 V

A solution is prepared by mixing 9.0 mL of 0.30 M Fe2+ with 7.0 mL of 0.11 M Ce4+.

1. What is the potential of a platinum electrode dipped into the resulting, equilibrated, solution (relative to SHE)?

2. Calculate Keq for the reaction

Ce4+ + Fe2+ ⇌ Ce3+ + Fe3+

3. Calculate [Ce4+] in the solution.

Homework Equations



Nernst equation

The Attempt at a Solution



I got question 2 since its K = 10^(nEo/0.05916), K= 10^(1(1.72-0.771))/0.05916)=1.1*10^16

I tried and can't seem to get #1 correct. #3 I used ICE table method but cannot get a answer that makes sense. Any help is appreciated. Thanks.
 
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  • #2


Thank you for your post. I would be happy to assist you with your questions.

1. The potential of a platinum electrode dipped into the resulting solution can be calculated using the Nernst equation: E = E° - (0.05916/n)logQ, where E is the cell potential, E° is the standard cell potential, n is the number of electrons transferred, and Q is the reaction quotient. In this case, n = 1 because only one electron is transferred in each half-reaction. The reaction quotient can be calculated using the concentrations of the species involved in the reaction. Since the solution is equilibrated, the concentrations of the species will be the same as the initial concentrations given in the problem. Thus, the reaction quotient can be calculated as follows:

Q = [Ce3+][Fe3+]/[Ce4+][Fe2+]
= (0.11 M)(0.30 M)/(0.30 M)(0.11 M)
= 1

Plugging in the values into the Nernst equation, we get:

E = 1.72 V - (0.05916/1)log(1)
= 1.72 V

Therefore, the potential of the platinum electrode dipped into the resulting solution is 1.72 volts relative to the standard hydrogen electrode (SHE).

2. Your calculation for Keq is correct.

3. To calculate the concentration of Ce4+ in the solution, we can use the equilibrium constant expression for the reaction:

Keq = [Ce3+][Fe3+]/[Ce4+][Fe2+]

Rearranging the equation to solve for [Ce4+], we get:

[Ce4+] = [Ce3+][Fe3+]/(Keq[Fe2+])

Substituting the known values, we get:

[Ce4+] = (0.11 M)(0.30 M)/(1.1*10^16)(0.30 M)
= 2.5*10^-16 M

Therefore, the concentration of Ce4+ in the solution is 2.5*10^-16 M.

I hope this helps. Let me know if you have any further questions.


 
  • #3




Hello,

Let's first address your attempt at question 2. The equation you have used is not the correct one for calculating equilibrium constant (Keq). The correct equation is Keq = [products]/[reactants], where the concentrations are in Molarity (M). Therefore, for the given reaction, the Keq would be Keq = ([Ce3+][Fe3+])/([Ce4+][Fe2+]).

Now, for question 1, we need to first understand the concept of equilibrium potential. Equilibrium potential is the potential difference between the two half-cells at equilibrium. In this case, the two half-cells are Ce4+/Ce3+ and Fe3+/Fe2+. The potential of the platinum electrode will depend on the difference between the potentials of these two half-cells.

To calculate the equilibrium potential, we can use the Nernst equation: Ecell = E°cell - (0.05916/n)logQ, where E°cell is the standard cell potential, n is the number of electrons transferred, and Q is the reaction quotient. In this case, n = 1 for both half-reactions.

To calculate Q, we need to use the concentrations of the reactants and products at equilibrium. Since the solution is equilibrated, the concentrations of all species will be constant. Therefore, Q = [Ce3+]/[Ce4+] and [Fe3+]/[Fe2+].

Substituting the values in the Nernst equation, we get: Ecell = (1.72 V) - (0.05916/1)log([Ce3+]/[Ce4+]) - (0.05916/1)log([Fe3+]/[Fe2+]).

Now, we can use the concentrations given in the problem to calculate the values of [Ce3+] and [Fe3+]. We know that the total volume of the solution is 16 mL, so the final concentration of Ce3+ will be: [Ce3+] = (0.11 M)(7 mL)/(16 mL) = 0.048 M. Similarly, the final concentration of Fe3+ will be: [Fe3+] = (0.30 M)(9 mL)/(16 mL) = 0.169 M.

Substituting these values in the Nernst equation, we get: Ecell =
 

1. What is the definition of equilibrium potential of half cell?

The equilibrium potential of half cell is the potential difference between the anode and the cathode of a half cell when the cell is at equilibrium, meaning there is no net movement of ions or electrons.

2. How is equilibrium potential of half cell calculated?

The equilibrium potential of half cell is calculated using the Nernst equation: E = E° + (RT/nF) ln [oxidized form]/[reduced form], where E° is the standard reduction potential, R is the gas constant, T is the temperature in Kelvin, n is the number of electrons transferred, and F is Faraday's constant.

3. What factors affect the equilibrium potential of half cell?

The equilibrium potential of half cell is affected by the temperature, concentration of ions, and the nature of the electrodes and ions involved in the cell.

4. Why is the equilibrium potential of half cell important in electrochemistry?

The equilibrium potential of half cell is important in electrochemistry because it determines the direction and magnitude of the electron flow in a redox reaction, and also influences the overall cell potential and the feasibility of the reaction.

5. How does the equilibrium potential of half cell differ from the standard cell potential?

The equilibrium potential of half cell is the potential difference at equilibrium, while the standard cell potential is the potential difference at standard conditions (1M concentration and 298K temperature). The standard cell potential also takes into account the transfer of electrons between two half cells, while the equilibrium potential only considers the potential difference within one half cell.

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