๐Ÿ’intro to chemistry review

Standard Reduction Potentials

Written by the Fiveable Content Team โ€ข Last updated September 2025
Written by the Fiveable Content Team โ€ข Last updated September 2025

Definition

Standard reduction potentials are a measure of the tendency of a chemical species to gain or lose electrons in an electrochemical reaction. They provide a quantitative assessment of the oxidizing or reducing power of a substance, which is crucial for understanding concepts like potential, free energy, and equilibrium in chemistry.

5 Must Know Facts For Your Next Test

  1. Standard reduction potentials are measured relative to the standard hydrogen electrode, which is assigned a value of 0 volts.
  2. Positive standard reduction potentials indicate that the species is a stronger oxidizing agent than hydrogen, while negative values indicate a weaker oxidizing agent.
  3. The difference in standard reduction potentials between two half-reactions determines the direction and spontaneity of the overall redox reaction.
  4. Standard reduction potentials are used to predict the feasibility and direction of electrochemical reactions, as well as the potential difference generated in a galvanic cell.
  5. The magnitude of the standard reduction potential is related to the free energy change of the reaction through the Nernst equation, which allows for the calculation of the equilibrium constant and spontaneity of the reaction.

Review Questions

  • Explain how standard reduction potentials are used to determine the direction and spontaneity of a redox reaction.
    • The difference in standard reduction potentials between the two half-reactions involved in a redox reaction determines the direction and spontaneity of the overall reaction. If the difference in standard reduction potentials is positive, the reaction will be spontaneous and the species with the higher reduction potential will be reduced, while the species with the lower reduction potential will be oxidized. Conversely, if the difference is negative, the reaction will be non-spontaneous, and energy will need to be supplied to drive the reaction in the desired direction.
  • Describe the relationship between standard reduction potentials, free energy, and the equilibrium constant of a redox reaction.
    • The standard reduction potential is directly related to the free energy change ($$\Delta G^\circ$$) of a redox reaction through the equation $$\Delta G^\circ = -nF\Delta E^\circ$$, where $n$ is the number of electrons transferred, $F$ is the Faraday constant, and $\Delta E^\circ$ is the difference in standard reduction potentials between the two half-reactions. The free energy change, in turn, is related to the equilibrium constant $K_\text{eq}$ through the equation $$\Delta G^\circ = -RT\ln K_\text{eq}$$, where $R$ is the gas constant and $T$ is the absolute temperature. Therefore, the standard reduction potentials can be used to calculate the free energy change and the equilibrium constant of a redox reaction, which are crucial for understanding the spontaneity and feasibility of the reaction.
  • Analyze how the Nernst equation can be used to predict the reduction potential of a half-cell under non-standard conditions.
    • The Nernst equation allows for the calculation of the reduction potential of a half-cell under non-standard conditions, such as when the concentrations of the reactants and products are not equal to 1 M. The Nernst equation is given by $$E = E^\circ - \frac{RT}{nF}\ln\left(\frac{[\text{Red}]}{[\text{Ox}]}\right)$$, where $E$ is the reduction potential under the given conditions, $E^\circ$ is the standard reduction potential, $R$ is the gas constant, $T$ is the absolute temperature, $n$ is the number of electrons transferred, $F$ is the Faraday constant, and $[\text{Red}]$ and $[\text{Ox}]$ are the concentrations of the reduced and oxidized species, respectively. By using the Nernst equation, one can predict how the reduction potential will change as the concentrations of the reactants and products vary, which is crucial for understanding the behavior of electrochemical systems under non-standard conditions.

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