Write the chemical reactions that show that 1 mol of I2 is required for 1 mol of H2O in a Karl Fischer titration.

Short Answer

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The chemical reaction that took place in Karl Fischer titration is stated below

ROH+SO2+BBH++ROSO2-H2O+I2+ROSO2-+2BROSO3-+2BH+I-

Step by step solution

01

Karl Fischer titration

The major application of Karl Fischer titration, is in the measurement of traces of water in transformer oil, polymers, solvents, foods, and other substances etc. This procedure is expected to be performed half a million times each day.

The titration is usually performed by delivering titrant from an automated burette or by coulometric generation of titrant. For large amount of water (but can go as low as~1mgH2O), the volumetric procedure is considered to be suitable whereas for very little amount of water the coulometric procedure is suitable.

02

Determine the Process End point in Karl Fischer titration

The anode solution (base, alcohol, SO2,I-) is poured in main section in above figure and cathodic solution which has reagents to be reduced at cathode is poured in coulometric generator. Current is passed till the end point. An unknown solution is fed via septum. After that the consumption of moisture is observed by coulometer. When the ratio of water and iodine is 1: 1, then 2 moles of e-corresponds to one mole of water.

ROH+SO2+BBH++ROSO2-H2O+I2+ROSO2-+2BROSO3-+2BH+I-

lodine molecule is generated on oxidizing in anode compartment. Then Iodine molecule oxidizes SO2to form ROSO3-. Therefore, one mole of iodine molecule is required to consume one mole of water.

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Most popular questions from this chapter

The standard free energy change for the formation of H2(g)=12O2(g) from H2O(l) is G°=+237.13KJ The reactions are

cathode:2H2O+2e-H2(g)+20H-Anode:H2O12O2(g)+2H++2e-

Calculate the standard voltageE°needed to decompose water into its elements by electrolysis. What does the word standard mean in this question?

Fundamentals of Electrolysis

17 - 6.The cell in Figure 17 - 4 is:

Cu|1.0MCuSO4(aq)|KCL(aq,3M)|AgCI(s)|Ag(s)

Write half-reactions for this cell. Neglecting activity coefficients and the junction potential betweenCuSO4(aq)and KCI(aq), predict the equilibrium (zero-current) voltage expected when the Lugging capillary contacts the electrode. For this purpose, suppose that the reference electrode potential is 0.197Vvs. S.H.E. Why is the observed equilibrium potential+109mV, not the value you calculated?

How would the over potentials change if>1.000Vwere imposed by the

Potentiostat?

A solution of Sn2+is to be electrolyzed to reduce the Sn2+to Sn(s). Calculate the cathode potential (versus S.H.E.) needed to reduce[Sn2+]to1.0×10-8Mif no concentration polarization occurs. What would be the potential versus S.C.E. instead of S.H.E? Would the potential be more positive or more negative if concentration polarization occurred?

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?

Ions that react with Ag+can be determined electrogravimetrically by deposition on a silver working anode:

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

(a) What will be the final mass of a silver anode used to electrolyze 75.00 mL of 0.02380 M KSCN if the initial mass of the anode is 12.4638 g?

(b) At what electrolysis voltage (versus S.C.E.) will AgBr(s) be deposited from 0.10M Br? (Consider negligible current flow, so that there is no ohmic potential, concentration polarization, or overpotential.)

(c) Is it theoretically possible to separate 99.99% of0.10M Klfrom0.10MKBr by controlled-potential electrolysis?

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