Calculate the molar concentration of the different colour solutions using the data table. (Available concentrations are: OM, 0.2M, 0.4M, 0.6M, 0.8M, and 1M). Also determine the isotonic point.
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- hree components in a mixture have varying distribution constants between the mobile phase and the stationary phass One of the components has a very low distribution constant, Would this component likely elute first or last and how would you design an experiment or modify the components of the separation to make it perform in the opposite manner?Structural elucidation of a sample component is possible through point estimation of its components with modern instrumentation methodologies. Additionally, characterization of their chemical nature is possible through qualitative analytical methods. A - If the first statement is TRUE and the second statement is FALSEB - If the first statement is FALSE and the second statement is TRUEC - If both statements are TRUED - If both statements are FALSEFor Indirect Iodometric Analysis of Copper... ~0.0896g KIO3 necessary to consume 350mL of 0.1 M Na2S2O3, Na2S2O3 is stored in an amber glass bottle until ready for use. Primary Standard KIO3 has 2g of KI, 50mL of DI water, and 10 mL of 1.0M HCl is added then immediately titrated with Na2S2O3 until medium yellow or straw... then 5mL of starch indicator is added and titrated again until blue black color turns clear. Unknown CuO use 1.2G of Unknown, 20mL of HNO3 heated until sample dissolved, 25 mL of DI water added and boiled until clear light blue color, after cooling 1:1 NH3 added (~34.47 mL of NH4OH reagent) until permanent deep blue color amine complex, 2g of NH4HF2 added and swirled until dissolved, 3 g of KI is added then titrated immediately with Na2S2O3 until brown color of iodide is nearly gone (brown milk color), 2 g of KSCN and 3 mL of starch indicator is then added with titration continuing until disappearance of new blue black color. 1. Na2CO3 is often added to thiosulfate…
- For Indirect Iodometric Analysis of Copper... ~0.0896g KIO3 necessary to consume 350mL of 0.1 M Na2S2O3, Na2S2O3 is stored in an amber glass bottle until ready for use. Primary Standard KIO3 has 2g of KI, 50mL of DI water, and 10 mL of 1.0M HCl is added then immediately titrated with Na2S2O3 until medium yellow or straw... then 5mL of starch indicator is added and titrated again until blue black color turns clear. Unknown CuO use 1.2G of Unknown, 20mL of HNO3 heated until sample dissolved, 25 mL of DI water added and boiled until clear light blue color, after cooling 1:1 NH3 added (~34.47 mL of NH4OH reagent) until permanent deep blue color amine complex, 2g of NH4HF2 added and swirled until dissolved, 3 g of KI is added then titrated immediately with Na2S2O3 until brown color of iodide is nearly gone (brown milk color), 2 g of KSCN and 3 mL of starch indicator is then added with titration continuing until disappearance of new blue black color. 4. Why is the starch indicator solution…a- Separation is essential in chemical analysis especially when we are dealing with complexmixture of chemical species. Name 1 separation technique based on basis of operation asbelow. Basis of operation Techniquei) Sizeii) Mass and densityiii) Change in physical stateWhat are the general characteristics of Gas Chromatography, Thin Layer Chromatography, Ion Exchange, HPLC, SEC and Affinity Chromatography? What elutes first? Additionally can you explain what exactly is stationary phase and mobile phase?
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- Provide a brief explanation of one specific application on High Performance Liquid Chromatography (HPLC). Incorporate the specific application name (e.g., Detection and Quantification of Mycotoxins), provide aconcise overview of sample preparation methods, outline instrumental parameters and conditions utilized, and summarize the outcomes and findings achieved through this analytical approach.Explain the meaning of the advantages of coulometry * No need to prepare, standardize, or store standard solutions. * Can prepare unstable reagents in situ (original place) since they react almost as soon as they are generated - e.g., C12, Br2 * Straightforward to generate tiny quantities of reagent with good accuracy since it is easy to control current and time electronically. * A single coulometric titration apparatus can be used for redox, acid/base, precipitation, complexometric, etc., titrations.Small explanation needed. In reverse-phased separations, _______ column volume(S) of initial solvent should be passed through the column after a gradient run to equilibrate the stationary phase with solvent for the next run. A) one B) two C) five D) ten E) twenty