Lead is to be deposited at a cathode from a solution that is 0.150 M in Pb2+ and 0.215 M in HClO4. Oxygen is evolved at a pressure of 0.850 atm at a 30-cm2platinum anode. The cell has a resistance of 0.900 V.

(a) Calculate the thermodynamic potential of the cell.

(b) Calculate the IR drop if a current of 0.220 A is to be used.

Short Answer

Expert verified

(a) The thermodynamic potential of the cell is -1.409 V.

(b) The IR drop when the current is 0.220 A is 0.198 V.

Step by step solution

01

Part (a) Step 1: Given Information

The thermodynamic potential of the cell should be determined.

02

Part (a) Step 2: Explanation

The solution is 0.150 M in Pb2+ and 0.215 M in HClO4.

The expression for electrode potential is:

Ecell=E0cell-0.0592nlog[Red][Ox]

Here, standard electrode potential is E0cell, number of electrons is n, reduction is Red and oxidation is Ox.

The electrode potential of the cell is equal to the difference between electrode potential of cathode and electrode potential of anode.

Ecell=Eright-Eleft…… (I)

Here, the electrode potential of cathode is Erightand electrode potential of anode is Eleft.

The overall reaction is:

2Pb2++2H2O2Pb(s)+O2+4H+

Write the reaction at cathode.

2Pb2++4e2Pb(s)

The reaction at anode is:

O2+4H++4e-2H2O

The expression for the electrode potential of cathode is:

Eright=E0cell-0.0592nlog1[Pb2+]2…… (II)

The expression for the electrode potential of anode is:

Eleft=E0cell-0.0592nlog1[pO2][H+]4…… (III)

Substitute -0.126 for , 2 for n and 0.150 for Pb2+ in equation (II).

Eright=-0.126-0.05924log1[0.150]2=-0.1504V

Substitute 1.299 for E0cell, 0.850 for pO2, 4 for n and 0.215 for H+ in equation (III).

Eleft=1.299-0.05924log1[0.850][0.215]4=1.2584V

Substitute -0.1504 V for Erightand 1.2584 V for Eleft.

Ecell=(-0.1504V)-(1.2584V)=-1.409V

Therefore, the thermodynamic potential of the cell is -1.409 V..

03

Part (b) Step 1: Given Information

The IR drop when the current is 0.220 A should be determined.

04

Part (b) Step 2: Explanation

The oxygen is evolved at pressure of 0.850 atm at a 30 cm2 platinum anode. And resistance of cell is 0.900 ohm.

The expression for IR drop is:

V=IR …… (IV)

Here, voltage of cell is V, the current is I and resistance of the cell is R.

Substitute 0.220 A for I and 0.900 ohm for R in Equation (IV).

V=(0.220A)(0.900Ω)=0.198V

Therefore, the IR drop is 0.198 V.

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Most popular questions from this chapter

A 0.0712-g sample of a purified organic acid was dissolved in an alcohol-water mixture and titrated with coulometrically generated hydroxide ions. With a current of 0.0392 A, 241 s was required to reach a phenolphthalein end point. Calculate the equivalent mass of the acid.

Calculate the time required for a constant current of 0.875 A to deposit 0.350 g of (a) Tl(III) as the element on a cathode, (b) Tl(I) as the Tl2O3 on an anode, and (c) Tl(I) as the element on a cathode.

Calculate the minimum difference in standard electrode potentials needed to lower the concentration of the metal M+ to 2.00 x 10-4 M in a solution that is 1.00 x 10-1 M in the less-reducible metal M2 where (a) M2 is univalent and M1 is divalent, (b) M2 and M1 are both divalent, (c) M2 is trivalent and M1 is univalent, (d) M2 is divalent and M1 is univalent, (e) M2 is divalent and M1 is trivalent.

Halide ions can be deposited at a silver anode, the reaction being

Ag1s2 1 X2 h AgX1s2 1 e2

Suppose that a cell was formed by immersing a silver anode in an analyte solution that was 0.0250 M Cl2,

Br2, and I2 ions and connecting the half-cell to a saturated calomel cathode via a salt bridge.

(a) Which halide would form first and at what potential? Is the cell galvanic or electrolytic?

(b) Could I2 and Br2 be separated quantitatively? (Take 1.00 3 1025

M as the criterion for quantitative

removal of an ion.) If a separation is feasible, what range of cell potential could be used?

(c) Repeat part (b) for I2 and Cl2.

(d) Repeat part (b) for Br2 and Cl2.

Construct a coulometric titration curve of 100.0 mL of a 1 M H2SO4 solution containing Fe(II) titrated with Ce(IV) generated from 0.075 M Ce(III). The titration is monitored by potentiometry. The initial amount of Fe(II) present is 0.05182 mmol. A constant current of 20.0 mA is used. Find the time corresponding to the equivalence point. Then, for about ten values of time before the equivalence point, use the stoichiometry of the reaction to calculate the amount of Fe3+ produced and the amount of Fe2+remaining. Use the Nernst equation to find the system potential. Find the equivalence point potential in the usual manner for a redox titration. For about ten times after the equivalence point, calculate the amount of Ce4+ produced from the electrolysis and the amount of Ce3+ remaining. Plot the curve of system potential versus electrolysis time.

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