Set up Mg(s)|Mg2+(1 M)||H+(1 M)|H2(1 bar), Pt. Magnesium acts as the anode and the standard hydrogen electrode acts as the cathode. Since E°SHE = 0, E°cell = 0 - E°Mg2+/Mg. Thus E°Mg2+/Mg = -E°cell measured under standard conditions.
Connect Mg2+|Mg as one half-cell with the standard hydrogen electrode and measure the standard cell emf.
Zinc is more reactive than copper and has a lower standard reduction potential. It will displace copper from copper sulphate solution: Zn(s) + Cu2+(aq) → Zn2+(aq) + Cu(s). Therefore copper sulphate solution cannot be stored in a zinc pot.
No.
Fe3+/Fe2+ has E° = +0.77 V. Any oxidising agent with a higher reduction potential can oxidise Fe2+ to Fe3+. Suitable examples include MnO4-/Mn2+ in acid, Cr2O7^2-/Cr3+ in acid, and Cl2/Cl-.
Examples are acidified KMnO4, acidified K2Cr2O7 and chlorine.
For 2H+(aq) + 2e- → H2(g), with pH2 = 1 bar, E = E° - (0.0591/2)log(1/[H+]^2) = -0.0591 pH. At pH = 10, E = -0.0591 x 10 = -0.591 V.
-0.591 V.
For Mg(s) + Cu2+(aq) → Mg2+(aq) + Cu(s), n = 2 and Q = [Mg2+]/[Cu2+] = 0.001/0.0001 = 10. Ecell = E°cell - (0.0591/2)log Q = 2.71 - (0.0591/2)log10 = 2.68 V.
2.68 V.
Here n = 2. ΔrG° = -nFE°cell = -2 x 96485 x 0.236 = -4.55 x 10^4 J mol^-1 = -45.5 kJ mol^-1. Also E°cell = (0.0591/n)log K at 298 K, so log K = nE°/0.0591 = 2(0.236)/0.0591 = 7.99. Hence K ≈ 9.7 x 10^7.
ΔrG° = -45.5 kJ mol^-1; K = 9.7 x 10^7.
Conductivity κ measures how well a solution conducts electricity and has units S m^-1 or S cm^-1. Molar conductivity Λm = κ x 1000/C when κ is in S cm^-1 and C in mol L^-1. Conductivity decreases on dilution because ions per unit volume decrease. Molar conductivity increases on dilution because interionic interactions decrease and ions move more freely; for weak electrolytes it increases sharply due to increased dissociation.
Conductivity is conductance of a solution of unit length and unit cross-section. Molar conductivity is conductivity of the volume of solution containing one mole of electrolyte.
Λm = κ x 1000/C = 0.0248 x 1000/0.20 = 124 S cm^2 mol^-1.
124 S cm^2 mol^-1.
Λm = κ x 1000/C = (7.896 x 10^-5 x 1000)/0.00241 = 32.76 S cm^2 mol^-1. Degree of dissociation α = Λm/Λm° = 32.76/390.5 = 0.0839. Ka = Cα^2/(1 - α) = 0.00241(0.0839)^2/(0.9161) = 1.85 x 10^-5.
Λm = 32.76 S cm^2 mol^-1; Ka = 1.85 x 10^-5.
Al3+ + 3e- → Al requires 3 mol electrons per mole Al3+, so charge = 3F. Cu2+ + 2e- → Cu requires 2F. In acidic solution, MnO4- + 8H+ + 5e- → Mn2+ + 4H2O, so 5F is required.
(i) 3 F; (ii) 2 F; (iii) 5 F.
For Ca2+ + 2e- → Ca, 1 mol Ca requires 2F. 20.0 g Ca = 0.500 mol, so charge = 0.500 x 2 = 1.0 F. For Al3+ + 3e- → Al, 40.0 g Al = 40.0/27.0 = 1.48 mol, so charge = 1.48 x 3 = 4.44 F.
(i) 1.0 F; (ii) 4.44 F.
For water oxidation, 2H2O → O2 + 4H+ + 4e-. Therefore 1 mol H2O corresponds to 2 mol electrons = 2F = 1.93 x 10^5 C. In FeO to Fe2O3, Fe2+ is oxidised to Fe3+, requiring 1 electron per Fe. Therefore 1 mol FeO requires 1F = 9.65 x 10^4 C.
(i) 2 F = 1.93 x 10^5 C; (ii) 1 F = 9.65 x 10^4 C.
Ni2+ + 2e- → Ni. Charge passed = It = 5 x 20 x 60 = 6000 C. Mass deposited = (MIt)/(nF) = (58.7 x 6000)/(2 x 96500) = 1.82 g.
1.82 g.
For Ag+ + e- → Ag, charge required for 1.45 g Ag is Q = (1.45/107.9)F = 1297 C. Time = Q/I = 1297/1.5 = 865 s. The same charge passes through all cells. Cu2+ + 2e- → Cu gives mass Cu = (63.5/2F)Q = 0.427 g. Zn2+ + 2e- → Zn gives mass Zn = (65.4/2F)Q = 0.439 g.
Time = 865 s; Cu deposited = 0.427 g; Zn deposited = 0.439 g.