/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Q2TY Suppose we wish to electrolyze I... [FREE SOLUTION] | 91影视

91影视

Suppose we wish to electrolyze I-to I3-in a 0.10M Klsolution containing 3.010-5MI3-at pH 10.00with PH2=1.00bar.

3I-+2H2OI3-+H2(g)+2OH-

(a) Find the cell voltage if no current is flowing.

(b) Then suppose that electrolysis increases [I3-]to3.010-4M, but other concentrations are unaffected. Suppose that the cell resistance is2.0, the current is 63 mA, the cathode overpotential is 0.382V, and the anode overpotential is 0.025 V. What voltage is needed to drive the reaction?

Find the voltage in part (b) ifrole="math" localid="1663645169401" [I-]s=0.01M.

Short Answer

Expert verified

The voltage required to complete the electrolysisI- toI3- is -1.732 V.

Step by step solution

01

Step1:

When the electric current is too small, the voltage of cell is given as

E=E (cathode)-E(anode)

E( cathode) is electrode's potential which is attached to the negative terminal of the current source.

E (anode) is electrode's potential which is attached to the positive terminal of the current source.

Overpotential:The activation energy of a reaction at an electrode can be overcome by voltage. The required voltage to apply is called overpotential.

Ohmic potential:In an electrochemical cell, the electrical resistance of a solution while current I flows can be overcome by voltage. The required voltage to apply is called ohmic potential.

Eohmic=IR

Concentration Polarization: It is the change in concentration of products and reactants at electrode's surface unlike they are same in solution.

02

Determine the voltage required to complete the electrolysis to .

Given,

The concentration ofI- is 0.01 M.

E( anode)0.535-0.059162log0.0130.0003=0.608V

E=E( cathode ) -E( anode )IR-overpoetentials

=-0.591V-0.608V-(2.0)(0.063A)-0.382V-0.025V=-1.732V

In order to drive the electrolysis of I-to role="math" localid="1663645612720" I3-,-1.732Vis required.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91影视!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Chemical oxygen demand by coulonetry. An electrochemical device incorporating photooxidation on a \({\rm{Ti}}{{\rm{O}}_2}\) surface could replace refluxing with \({{\rm{C}}_2}{\rm{O}}_7^{2 - }\) to measure chemical oxygen demand (Box 16-2). The diagram shows a working electrode beld at \( + 0.30\;{\rm{V}}\) versus \({\rm{Ag}}\mid {\rm{AgCl}}\) and coated with nanoparticles of 'TiO . Wltraviolet2inradiation generates electrons and holes in \({{\rm{T}}_1}{{\rm{O}}_2}\). Holes oxidize

organic matter at the surface. Electrons reduce \({{\rm{H}}_2}{\rm{O}}\) at the auxiliary electrode in a compartment connected to the working compartment by a salt bridge. The sample compartment is only 0.18 mm thick with a volume of \(13.5\mu \,{\rm{L}}\). It requires \(\~1\;\,{\rm{min}}\) for all organic matter to diffuse to the \({\rm{Ti}}{{\rm{O}}_2}\) surface and be exhaustively oxidized.

Left: Working electrode. Fight Photocument response for sample and blank Both solutions contain \(2{\rm{M}}\,{\rm{NaNO}}\). (Dst from H zhso, D. fisng. 5 . zhang K. Cutteral, and R. Jshn, "Development of a Drect Fhotselectrocherrical Method for Deterrination of Gherrical Ouygen Demand," And. Chan. 2004, 76 155.)

The blank curve in the graph shows the response when the sample compartment contains just electrolyte. Before inradiation, no current is observed. Ultraviolet radiation causes a spike in the current, followed by a decrease to a steady level near \(40\mu \). This current arises from oxidation of water at the \({\rm{Ti}}{{\rm{O}}_2}\)sufface under ultraviolet exposure. The upper curve sbows the same experiment, but with wastewater in the sample compartment. The increased current arises from oxidation of organic matter. When the organic matter is consumed, the cument decreases to the blank level. The area between the two curves tells us how many electrons flow from oxidation of organic matter in the sample.

  1. Balance the oxidation half-reaction that occurs in this cell:

\({{\rm{C}}_e}{{\rm{H}}_k}{{\rm{O}}_a}\;{{\rm{N}}_s}{{\rm{X}}_x} + {\rm{A}}{{\rm{H}}_2}{\rm{O}} \to {\rm{BC}}{{\rm{O}}_2} + {\rm{CX}} + {\rm{DN}}{{\rm{H}}_3} + {\rm{E}}{{\rm{H}}^ + } + {\rm{F}}{{\rm{e}}^ - }\)

where X is any halogen. Express the stoichiometry coefficients A, B, C, D, E, and F in terms of c, h, o, n, and x.

  1. How many molecules of \({{\rm{O}}_2}\)are required to balance the halfreaction in part (a) by reduction of oxygen (\({{\rm{O}}_2} + 4{{\rm{H}}^ + } + 4{{\rm{e}}^ - } \to 2{{\rm{H}}_2}{\rm{O}}\))?
  2. The area between the two curves in the graph is \(\int_0^\infty {({I_{{\rm{sample }}}}} - {I_{blank}})dt = 9.43\,{\rm{mC}}{\rm{.}}\) This is the number of electrons liberated by complete oxidation of the sample. How many moles of \({{\rm{O}}_2}\) would be required for the same oxidation?
  3. Chemical oxygen demand (COD) is expressed as mg of \({{\rm{O}}_2}\) required to oxidize 1 L of sample. Find the COD for this sample.
  4. If the only caidizable substance in the sample were \({{\rm{C}}_9}{{\rm{H}}_6}{\rm{N}}{{\rm{O}}_2}{\rm{CIB}}{{\rm{r}}_2}\). what is its concentration in molL?

Explain what is done in anodic stripping voltammetry. Why is stripping the most sensitive voltammetric technique?

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 脳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, 鈥淐yclic Voltammetry,鈥 J. Chem. Ed. 1983, 60, 702.]

Explain how the endpoint is detected in a Karl Fischer titration in Figure 17-35.

Chlorine has been used for decades to disinfect drinking water. An undesirable side effect of this treatment is reaction with organic impurities to create organochlorine compounds, some of which could be toxic. Monitoring total organic halide (designated TOX) is required for many water providers. A standard procedure for TOX is to pass water through activated charcoal, which adsorbs organic compounds. Then the charcoal is combusted to liberate hydrogen halides:

Organichalide(RX)o2/800CCO2+H2O+HX

HX is absorbed into aqueous solution and measured by coulometric titration with a silver anode:

X-(aq)+Ag(s)AgX(s)+e-

When 1.00 L of drinking water was analyzed, a current of 4.23 mA was required for 387 s. A blank prepared by oxidizing charcoal required 6 s at 4.23 mA. Express the TOX of the drinking water as mol halogen/L. If all halogen is chlorine, express the TOX as gCI/L.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.