Exercises: Cells, potentials and spontaneity
You have a Daniell galvanic cell made up of a zinc electrode immersed in a $1.0\text{ M}$ solution of $\mathrm{ZnSO_4}$ and a copper electrode immersed in a…
You have a Daniell galvanic cell made up of a zinc electrode immersed in a $1.0\text{ M}$ solution of $\mathrm{ZnSO_4}$ and a copper electrode immersed in a $1.0\text{ M}$ solution of $\mathrm{CuSO_4}$, at $25\text{ }^\circ\mathrm{C}$. The standard reduction potentials are $E^\circ(\mathrm{Zn}^{2+}/\mathrm{Zn}) = -0.76\text{ V}$ and $E^\circ(\mathrm{Cu}^{2+}/\mathrm{Cu}) = +0.34\text{ V}$.
- a) Write the conventional cell notation or diagram, indicating the anode and the cathode.
- b) State the sign or polarity assigned to each electrode and briefly justify which half-reaction takes place at each.
Consider a galvanic cell under standard conditions ($25\text{ }^\circ\mathrm{C}$, concentrations $1.0\text{ M}$) based on the overall reaction:…
Consider a galvanic cell under standard conditions ($25\text{ }^\circ\mathrm{C}$, concentrations $1.0\text{ M}$) based on the overall reaction: $\mathrm{Cu(s)} + 2\,\mathrm{Ag^+}(\text{aq}) \rightarrow \mathrm{Cu}^{2+}(\text{aq}) + 2\,\mathrm{Ag(s)}$. Data: $E^\circ(\mathrm{Ag}^+/\mathrm{Ag}) = +0.80\text{ V}$ and $E^\circ(\mathrm{Cu}^{2+}/\mathrm{Cu}) = +0.34\text{ V}$.
- a) Calculate the standard electromotive force of the cell, $E^\circ_{\text{pila}}$.
- b) Justify in detail why the standard reduction potential of the $\mathrm{Ag}^+/\mathrm{Ag}$ couple must not be multiplied by the stoichiometric coefficient 2 when calculating the emf of the cell.
For a cell made up of the couples $\mathrm{Ni}^{2+}/\mathrm{Ni}$ and $\mathrm{Cd}^{2+}/\mathrm{Cd}$ at $25\text{ }^\circ\mathrm{C}$, the overall spontaneous reaction…
For a cell made up of the couples $\mathrm{Ni}^{2+}/\mathrm{Ni}$ and $\mathrm{Cd}^{2+}/\mathrm{Cd}$ at $25\text{ }^\circ\mathrm{C}$, the overall spontaneous reaction under standard conditions is $\mathrm{Cd(s)} + \mathrm{Ni}^{2+}(\text{aq}) \rightarrow \mathrm{Cd}^{2+}(\text{aq}) + \mathrm{Ni(s)}$, the standard electromotive force being $E^\circ_{\text{pila}} = +0.15\text{ V}$. Data: Faraday constant $F = 96485\text{ C}\times\text{mol}^{-1}$.
- a) Determine the value of the standard Gibbs energy change, $\Delta G^\circ$, in $\text{kJ}\times\text{mol}^{-1}$.
- b) Deduce the criterion for spontaneity from the sign of $\Delta G^\circ$ and $E^\circ_{\text{pila}}$.
In the laboratory, a Daniell galvanic cell is set up at $25\text{ }^\circ\mathrm{C}$ with metallic zinc and copper electrodes immersed in $1.0\text{ M}$ aqueous…
In the laboratory, a Daniell galvanic cell is set up at $25\text{ }^\circ\mathrm{C}$ with metallic zinc and copper electrodes immersed in $1.0\text{ M}$ aqueous solutions of their respective cations, connected by a salt bridge of $\mathrm{KNO_3}$. The diagram of the experimental set-up is shown below:
Data: $E^\circ(\mathrm{Zn}^{2+}/\mathrm{Zn}) = -0.76\text{ V}$; $E^\circ(\mathrm{Cu}^{2+}/\mathrm{Cu}) = +0.34\text{ V}$.
- a) Determine the standard electromotive force of the cell and state the correct direction of electron flow through the external metallic conductor.
- b) Explain which species carries the charge through the salt bridge and towards which beaker the $\mathrm{K^+}$ and $\mathrm{NO_3^-}$ ions migrate respectively, stating why electrons do not flow through the solution.
A galvanic cell is built by connecting a half-cell with a chromium rod immersed in $\mathrm{Cr(NO_3)3}\text{ }1.0\text{ M}$ and another with a lead rod in…
A galvanic cell is built by connecting a half-cell with a chromium rod immersed in $\mathrm{Cr(NO_3)_3}\text{ }1.0\text{ M}$ and another with a lead rod in $\mathrm{Pb(NO_3)_2}\text{ }1.0\text{ M}$, at $25\text{ }^\circ\mathrm{C}$, using a salt bridge saturated with $\mathrm{NH_4NO_3}$. Data: $E^\circ(\mathrm{Cr}^{3+}/\mathrm{Cr}) = -0.74\text{ V}$, $E^\circ(\mathrm{Pb}^{2+}/\mathrm{Pb}) = -0.13\text{ V}$, $F = 96485\text{ C}\times\text{mol}^{-1}$.
- a) Write the anode and cathode half-equations and the balanced overall ionic equation, and calculate the standard potential of the cell.
- b) Explain how electroneutrality is maintained in each half-cell, specifying the movement of the salt bridge ions, and calculate the value of $\Delta G^\circ$ for the overall reaction.
The feasibility of a cell based on the standard couples $\mathrm{Fe}^{3+}/\mathrm{Fe}^{2+}$ and $\mathrm{I_2}/\mathrm{I^-}$ at $25\text{ }^\circ\mathrm{C}$ is analysed,…
The feasibility of a cell based on the standard couples $\mathrm{Fe}^{3+}/\mathrm{Fe}^{2+}$ and $\mathrm{I_2}/\mathrm{I^-}$ at $25\text{ }^\circ\mathrm{C}$ is analysed, with reactants under standard conditions. Data: $E^\circ(\mathrm{Fe}^{3+}/\mathrm{Fe}^{2+}) = +0.77\text{ V}$; $E^\circ(\mathrm{I_2}/\mathrm{I^-}) = +0.54\text{ V}$; $F = 96485\text{ C}\times\text{mol}^{-1}$.
- a) Write the balanced equation of the spontaneous redox reaction under standard conditions, identify the oxidising and reducing species, and calculate $E^\circ_{\text{pila}}$ and $\Delta G^\circ$.
- b) A student claims that, because $\Delta G^\circ < 0$, the reaction will always be spontaneous at any concentration and in any experimental context. Justify, with reasoning, why this claim is false, analysing the difference between $\Delta G^\circ$ and $\Delta G$.
You have aqueous solutions containing chloride ($\mathrm{Cl^-}$), bromide ($\mathrm{Br^-}$) and iodide ($\mathrm{I^-}$) ions, all at concentration $1.0\text{ M}$ and at…
You have aqueous solutions containing chloride ($\mathrm{Cl^-}$), bromide ($\mathrm{Br^-}$) and iodide ($\mathrm{I^-}$) ions, all at concentration $1.0\text{ M}$ and at $25\text{ }^\circ\mathrm{C}$. You want to select an oxidising agent in its standard state that is able to spontaneously oxidise the iodide ion to molecular iodine ($\mathrm{I_2}$), and the bromide ion to liquid bromine ($\mathrm{Br_2}$), but that does not oxidise the chloride ion to chlorine gas ($\mathrm{Cl_2}$).
Standard reduction potential data at $25\text{ }^\circ\mathrm{C}$:
$E^\circ(\mathrm{I_2}/\mathrm{I^-}) = +0.54\text{ V}$; $E^\circ(\mathrm{Br_2}/\mathrm{Br^-}) = +1.07\text{ V}$; $E^\circ(\mathrm{Cl_2}/\mathrm{Cl^-}) = +1.36\text{ V}$.
Oxidising agent candidates: $\mathrm{Fe}^{3+}(\text{aq})$ with $E^\circ(\mathrm{Fe}^{3+}/\mathrm{Fe}^{2+}) = +0.77\text{ V}$; $\mathrm{IO_3^-}(\text{aq})/\mathrm{I_2(s)}$ in acidic medium with $E^\circ = +1.20\text{ V}$; $\mathrm{MnO_4^-}(\text{aq})/\mathrm{Mn}^{2+}(\text{aq})$ in acidic medium with $E^\circ = +1.51\text{ V}$.
- a) Select the most suitable oxidising agent, justifying your answer by comparing the potentials of the candidates and calculating $E^\circ$ and $\Delta G^\circ$ for the reaction of the chosen oxidising agent with each halide, using the lowest whole-number coefficients.
- b) Write the balanced overall reaction that takes place between the selected oxidising agent and the bromide ion in acidic medium. Data: $F = 96485\text{ C}\times\text{mol}^{-1}$.
A metal sheet containing a mixture of cadmium, silver and iron is placed in solutions of acids and salts at $25\text{ }^\circ\mathrm{C}$ to evaluate displacement…
A metal sheet containing a mixture of cadmium, silver and iron is placed in solutions of acids and salts at $25\text{ }^\circ\mathrm{C}$ to evaluate displacement reactions.
Data: $E^\circ(\mathrm{Ag}^+/\mathrm{Ag}) = +0.80\text{ V}$; $E^\circ(\mathrm{H}^+/\mathrm{H_2}) = 0.00\text{ V}$; $E^\circ(\mathrm{Pb}^{2+}/\mathrm{Pb}) = -0.13\text{ V}$; $E^\circ(\mathrm{Cd}^{2+}/\mathrm{Cd}) = -0.40\text{ V}$; $E^\circ(\mathrm{Fe}^{2+}/\mathrm{Fe}) = -0.44\text{ V}$. Constant $F = 96485\text{ C}\times\text{mol}^{-1}$.
- a) Determine which metals in the sheet will dissolve spontaneously in an aqueous $1.0\text{ M}$ solution of hydrochloric acid ($\mathrm{HCl}$), releasing hydrogen gas under standard conditions, and write the corresponding reactions.
- b) If a piece of pure iron metal is immersed in a solution containing $\mathrm{Pb}^{2+}$ and $\mathrm{Cd}^{2+}$ ions, both at standard concentration $1.0\text{ M}$, reason quantitatively whether the iron will displace one, both or neither of these cations from the solution, calculating the standard emf and $\Delta G^\circ$ of the processes that are spontaneous. Use the thermodynamic model of standard potentials, without dissolved oxygen, complexation or passivation; the prediction does not give information about the actual rate.