Chapter 17: Q42P (page 431)
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
The chemical reaction that took place in Karl Fischer titration is stated below
Chapter 17: Q42P (page 431)
Write the chemical reactions that show that 1 mol of I2 is required for 1 mol of H2O in a Karl Fischer titration.
The chemical reaction that took place in Karl Fischer titration is stated below
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Get started for freeThe standard free energy change for the formation of from is The reactions are
Calculate the standard voltageneeded 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:
Write half-reactions for this cell. Neglecting activity coefficients and the junction potential betweenand 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 reducetoif 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.
\({{\rm{C}}_e}{{\rm{H}}_k}{{\rm{O}}_a}\;{{\rm{N}}_s}{{\rm{X}}_x} + {\rm{A}}{{\rm{H}}_2}{\rm{O}} \to {\rm{BC}}{{\rm{O}}_2} + {\rm{CX}} + {\rm{DN}}{{\rm{H}}_3} + {\rm{E}}{{\rm{H}}^ + } + {\rm{F}}{{\rm{e}}^ - }\)
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.
Ions that react with can be determined electrogravimetrically by deposition on a silver working anode:
(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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