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Explain the Brønsted-Lowry concept of acids, calculate the pH of a 0.001 M H2SO4 solution, define heterogeneous catalysts, and identify the strongest oxidizing and reducing agents based on standard el

Chemistry

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2 parts
e(i)

MnO4−(aq)MnO_4^-(aq)

Pb(s)

e(ii)

Pb(s)∣Pb2+(aq)∣∣I2(aq)∣I−(aq)Pb(s) | Pb^{2+}(aq) || I_2(aq) | I^-(aq)

0.67 V0.67 \text{ V}

Step-by-step solution

4 steps

Part d(i)

An acid, according to the Brønsted-Lowry concept, is a proton donor. It donates a hydrogen ion (H+H^+) to another substance.

Part d(ii)· 2 steps

Step 1: Write the dissociation equation for sulfuric acid (H2SO4H_2SO_4).

Sulfuric acid is a strong acid and dissociates completely in water.

H2SO4(aq)→2H+(aq)+SO42−(aq)H_2SO_4(aq) \to 2H^+(aq) + SO_4^{2-}(aq)
  1. Determine the concentration of H+H^+ ions.

    From the dissociation equation, 1 mole of H2SO4H_2SO_4 produces 2 moles of H+H^+ ions.
    Given concentration of H2SO4=0.001 MH_2SO_4 = 0.001 \text{ M}.
    Concentration of H+=2×0.001 M=0.002 MH^+ = 2 \times 0.001 \text{ M} = 0.002 \text{ M}.

  2. Calculate the pH using the formula pH=−log⁡[H+]pH = -\log[H^+].

    pH=−log⁡(0.002)pH = -\log(0.002) pH=−log⁡(2×10−3)pH = -\log(2 \times 10^{-3}) pH=−(log⁡2+log⁡10−3)pH = -(\log 2 + \log 10^{-3}) pH=−(0.301−3)pH = -(0.301 - 3) pH=−(−2.699)pH = -(-2.699) pH=2.699pH = 2.699

    The pH of the solution is approximately 2.70.

Part d(iii)

A heterogeneous catalyst is a catalyst that is in a different phase from the reactants. For example, a solid catalyst used in a reaction involving gaseous or liquid reactants.

Part e(i)

MnO4−(aq)MnO_4^-(aq)

To identify the strongest oxidizing and reducing agents, we look at the standard electrode potentials (E∘E^\circ).

  • The strongest oxidizing agent is the species on the left side of the half-reaction with the most positive (or least negative) E∘E^\circ value. This species is most easily reduced.
  • The strongest reducing agent is the species on the right side of the half-reaction with the most negative (or least positive) E∘E^\circ value. This species is most easily oxidized.

Given electrode potentials:
A: Pb2+(aq)+2e−→Pb(s)Pb^{2+}(aq) + 2e^- \to Pb(s), E∘=−0.13 VE^\circ = -0.13 \text{ V}
B: I2(aq)+2e−→2I−(aq)I_2(aq) + 2e^- \to 2I^-(aq), E∘=+0.54 VE^\circ = +0.54 \text{ V}
C: MnO4−(aq)+8H+(aq)+5e−→Mn2+(aq)+4H2O(l)MnO_4^-(aq) + 8H^+(aq) + 5e^- \to Mn^{2+}(aq) + 4H_2O(l), E∘=+1.51 VE^\circ = +1.51 \text{ V}

Comparing the E∘E^\circ values: +1.51 V+1.51 \text{ V} is the most positive.
The strongest oxidizing agent is MnO4−(aq)MnO_4^-(aq).
Comparing the E∘E^\circ values: −0.13 V-0.13 \text{ V} is the most negative.
The strongest reducing agent is Pb(s)Pb(s).

Strongest oxidizing agent: MnO4−(aq)\boxed{MnO_4^-(aq)}
Strongest reducing agent: Pb(s)\boxed{Pb(s)}

Part e(ii)

Pb(s)∣Pb2+(aq)∣∣I2(aq)∣I−(aq)Pb(s) | Pb^{2+}(aq) || I_2(aq) | I^-(aq)

Step 1: Determine the anode and cathode when cells A and B are coupled.

For a spontaneous reaction, the species with the more positive E∘E^\circ will be reduced (cathode), and the species with the more negative E∘E^\circ will be oxidized (anode).
Cell A: Pb2+(aq)+2e−→Pb(s)Pb^{2+}(aq) + 2e^- \to Pb(s), E∘=−0.13 VE^\circ = -0.13 \text{ V}
Cell B: I2(aq)+2e−→2I−(aq)I_2(aq) + 2e^- \to 2I^-(aq), E∘=+0.54 VE^\circ = +0.54 \text{ V}

Since EB∘(+0.54 V)E^\circ_B (+0.54 \text{ V}) is more positive than EA∘(−0.13 V)E^\circ_A (-0.13 \text{ V}), reaction B will occur at the cathode (reduction) and reaction A will occur at the anode (oxidation, reversed).

Anode (oxidation): Pb(s)→Pb2+(aq)+2e−Pb(s) \to Pb^{2+}(aq) + 2e^-
Cathode (reduction): I2(aq)+2e−→2I−(aq)I_2(aq) + 2e^- \to 2I^-(aq)

  1. Write the cell diagram.

    The cell diagram notation is: Anode | Anode ion || Cathode ion | Cathode.
    Pb(s)∣Pb2+(aq)∣∣I2(aq)∣I−(aq)\boxed{Pb(s) | Pb^{2+}(aq) || I_2(aq) | I^-(aq)}

  2. Calculate the electromotive force (emf) of the cell.

    Ecell∘=Ecathode∘−Eanode∘E^\circ_{cell} = E^\circ_{cathode} - E^\circ_{anode}
    Ecell∘=EB∘−EA∘E^\circ_{cell} = E^\circ_B - E^\circ_A
    Ecell∘=(+0.54 V)−(−0.13 V)E^\circ_{cell} = (+0.54 \text{ V}) - (-0.13 \text{ V})
    Ecell∘=0.54 V+0.13 VE^\circ_{cell} = 0.54 \text{ V} + 0.13 \text{ V}
    Ecell∘=0.67 VE^\circ_{cell} = 0.67 \text{ V}

    The emf of the cell is 0.67 V\boxed{0.67 \text{ V}}.

Part e(iii)

Electrons flow from the anode to the cathode in the external circuit.

In this cell, Pb(s)Pb(s) is oxidized at the anode, and I2(aq)I_2(aq) is reduced at the cathode.
Therefore, electrons will flow from the lead electrode (Pb) to the iodine electrode (I2_2).

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