Chapter 17: Q43P (page 431)
Explain how the endpoint is detected in a Karl Fischer titration in Figure 17-35.
Short Answer
The process of detection of endpoint in Karl Fischer titration.
Chapter 17: Q43P (page 431)
Explain how the endpoint is detected in a Karl Fischer titration in Figure 17-35.
The process of detection of endpoint in Karl Fischer titration.
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Get started for freeThe chlor-alkali process 54in which seawater is electrolyzed to make CI2 andNaOH, is the second most important commercial electrolysis, behindAIproduction.
Anode:
HgCathode:
The Nafion membrane (page 421) used to separate the anode and cathode compartments resists chemical attack. Its anionic side chains permit conduction ofNa+ , but not anions. The cathode compartment contains pure water, and the anode compartment contains seawater from which Ca2+ and Mg2+ have been removed. Explain how the membrane allows NaOH to be formed free ofNaCI.
Will(cathode) =0.19 Vreduce at pH 2 by the reaction?
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.
is to be generated in for coulometric reduction of azobenzene.
At the counter electrode, water is oxidized, and \(\mathrm{O}_{2}\) is liberated at a pressure of \(0.20\) bar. Both electrodes are made of smooth Pt, and each has a total surface area of . The rate of reduction of the azobenzene is 25.9nmol/s , and the resistance of the solution between the generator electrodes is .
Explain what is done in anodic stripping voltammetry. Why is stripping the most sensitive voltammetric technique?
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