What cathode potential (versus S.H.E.) is required to reduce 99.99%of cd(II) from a solution containing 0.10Mcd (II) in 1,0M ammonia if there is negligible current? Consider the following reactions and assume that nearly all (II) is in the form Cd(NH3)42+

localid="1663647104121" Cd2++4NH3Cd(NH3)42+β4=3.6×106Cd2++2e-Cd(s)E°=-.402V

Short Answer

Expert verified

The potential of cathode is E=-0.744 V

Step by step solution

01

Electrogravimetric Analysis

  • Separation along with the quantification of metals are mainly observed in electrogravimetric analysis.
  • Electrolysis of the analyte solution is done during this procedure.
02

Determine the lead lactate

Given data:

CdII=0.10MNH3=1Mβ4=3.6×106E°=-0.402VE=?

First we need to calculate Cd2+

β4=CdNH342+Cd2+NH34

99.99% Of Cd is reduced, so the concentration of CdNH342+is then:

CdNH342+=CdII-Cdll.0.9999CdNH342+=0.10M-0.10M.0.9999CdNH342+=1×10-5M

The concentration of Cd2+is:

Cd2+=CdNH342+NH34.βCd2+=1×10-5M14M×3.6×106Cd2+=2.78×10-12M

The potential of cathode is

Ecathod=E°-0.059162.log1Cd2+Ecathod=-0.402V-0.059162.log12.78.10-12Ecathod=-0.744V

The potential of cathode is E = -0.744V

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Most popular questions from this chapter

The cyclic voltammogram of the antibiotic chloramphenicol (abbreviated) is shown here. The first cathodic scan goes from 0 to -1.0 V. The first cathodic wave, , is from the reaction RNO2+4e-+4H+RNHOH+H2O. Peak B in the reverse anodic scan could be assigned to RNHOHRNO+2H++2e-. In the second cathodic scan from +0.9 to -0.4 V, the new peak C appears. Write a reaction for peak C and explain why peak C was not seen in the initial scan.


Cyclic voltammogram of 3.7 ×10-4 chloramphenicol in 0.1 M acetate buffer, pH 4.62. The voltage of the carbon paste working electrode was scanned at a rate of 350 mV/s. [Data from P. T. Kissinger and W. R. Heineman, “Cyclic Voltammetry,” J. Chem. Ed. 1983, 60, 702.]

(a) At what cathode potential will Sb(s)deposition commence from 0.010MSbO+solution at pH 0.00? Express this potential versus S.H.E. and versusAg|AgCI. (Disregard overpotential, about which you have no information.)

SbO++2H++3e-Sb(s)+H2OE°=0.208V

(b) What percentage of0.10MCu2+could be reduced electrolytically to Cu(s)before0.010MSbO+in the same solution begins to be reduced at pH 0.00?

What is the purpose of the Nafion the membrane in Figure 17-33

For a rotating disk electrode operating at sufficiently great potential, the redox reaction rate is governed by the rate at which analyte diffuses through the diffusion layer to the electrode (Figure 17-15b). The thickness of the diffusion layer is

δ=1.61D1/3V1/6ω-1/2

whereis the diffusion coefficient of reactant (m2/s),vis the kinematic viscosity of the liquid

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localid="1655441445229" Currentdebsity=0.62nFD2/3v-1/6ω1/2C0

where nis the number of electrons in the half-reaction, Fis the Faraday constant, and localid="1655441459070" C0is the concentration of the electroactive species in bulk solution localid="1655441466748" (mol/m3,notmol/L) Consider the oxidation oflocalid="1655441474339" Fe(CN)64-in a solution of localid="1655441479067" 10.0mMK3Fe(CN)6+50.0mMK4Fe(CN)6at +0.90V(versus S.C.E.) at a rotation speed oflocalid="1655441490849" role="math" 2.00×103revolutions per minute. 27The diffusion coefficient oflocalid="1655441497131" Fe(CN)64-is2.5×10-9m2/sand the kinematic viscosity islocalid="1655441503345" 1.1×10-5m2/sCalculate the thickness of the diffusion layer and the current density. If you are careful, the current density should look like the value in Figure 17-16b.

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