ghe mau speetla foremiela organometallie compound B Mo esHs (u)C,0, exhibit peake at m/z an 282, as4, 226, 198, 133 & 98 amu. What is ik probable aMuctuu
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- Calculate the amount of phycocyanin in Sample 1 in mg where A620=0.211 and A650=0.086, taking into account the dilution factor as per question 6 (100ul), and the total volume of extract as per question 4 (140ml) . Note your answer to 2 decimal placesCalculate the amount of phycocyanin in Sample 1 in mg where A620 = 0.193 and A650 = 0.095, taking into account the dilution factor of 100 ul, and the total volume of extract 45ml. Note your answer to 2 decimal places.Elaborat ur answer pls thank u
- Hello, I would like help with problem 42 in the image attached.A sample of steel (0.506 g) was digested in acid and the solution made up to 100 cm3 with deionised water. Aliquots (25.0 cm3) of this solution were transferred into two volumetric flasks (100 cm3) labelled A and B. Flask A was made up to volume with deionised water. To flask B was added 10.0 cm3 of a 260 ppm standard solution of Mn2+ which was then also made up to volume with deionised water. The following absorbance results were obtained: Solution A = 0.356, Solution B = 0.578. Use these results to calculate the percentage (% w/w) of manganese in the steel sample.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. 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…In the development o f an analytical method for the quantitative analysis o f iron using Atomic Absorption spectrophotometry (AAS), a linear calibration curve for standards o f 0.00, 5.00, 10.00, 15.00 and 20.00 ppm was prepared. An iron ore sample with an expected iron content o f 40-60% w/w is to be analysed by this method. An approximately 0.5-g sample is taken, dissolved in a minimum amount o f concentrated HC1 and diluted to 1 L in a volumetric flask using distilled water. A 5.00-mL aliquot is removed with a pipette. With explanation, to what volume (10, 25, 50, 100, 250 500 or 1000 mL) should the 5.00 mL aliquot be diluted, to minimize the uncertainty in the analysis?Solution for 0.105g of the K3[Fe(C2O4)3] (MW= 437.2 g/ mol) were dissolved in sulfuric acid and got rated with 9 mL of 0.028M KMn04. What is the experimental weight percent of oxalate in the sample?