2. Use the trendline equation from the calibration plot (that you wrote down in Table 2) to calculate the concentration of the unknown solution. Hint: the trendline equation is in the format of y = mx + b, where y is the absorbance (from Table 2) and x is the unknown concentration (that you will solve for). Try to show your work by typing into the group discussion, or you have the option to hand-write and submit a picture of your hand- written work.
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- Preparing a standard curve. 1. determine the absorbance max of [FeSCN]2+ it is 448.1 2. determine the concentration of FeSCN2+ in the stock solution. M1V1=M2V2 stock solution: ~0.200 M iron (iii) nitrate in 1M nitric acid intial volume: 0.3mL final volume: 10.3mL volume: 10mL ~0.002M potassium thiocyanate initial volume: 0.3mL final volume: 10.3mL volume: 10mL not sure if this is needed stock solutions: ~0.200M iron (iii) nitrate in 1M nitric acid: 0.207M ~0.002M iron (iii) nitrate in 1M nitric acid: 0.00209M ~0.002M potassium thiocyanate: 0.00193MA solution of Tryptophan has an absorbance at 280 nm of 0.54 in a 0.5 cm length cuvette. Given the absorbance coefficient of trp is 6.4 x 103 Lmol-1cm-1. What is the concentration of solution?Using the absorbance of [FeSCN]+2 at the wavelength of maximum absorption which you obtained in part B, and the diameter of the tube, obtained in part A,calculate the molar extinction coefficient. given info: Concentration of Fe3+ stock solution, C1 = 0.001 M Volume of stock Fe3+ solution pipetted, V1 = 25mL Concentration of diluted stock solution, C2 = 0.0004 M Volume of Fe2+ solution and KSCN (upon mixing) = 10mL Weight of KSCN = 1g The reaction taking place is given as: The reaction taking place is given as: F e 3+ (aq) + SC N − (aq) ⇔Fe [SCN] 2+ (aq) the concentration of [FeSCN]2+ after the mixing of Fe3+ and SCN- is 2.5 x 10-3 M. Moles of [FeSCN]2+ = 2.5 x 10-5 moles Diameter:1.2cm The wavelength at which maximum absorption takes place is = 480 nm
- Lead in dry river sediment was extracted with 25 wt% HNO3 at incubation temperatures for 1 hr. Then 1 mL of filtered extract was combined with other reagents to a total of 4.60 mL. Pb+2 was measured by an electrochemical method by spiking with 2.50 ppm Pb2+. added vol. of 2.50ppm Pb2 signal 0 mL 1.10 0.025 mL 1.66 .050 mL 2.20 .075 mL 2.81 what is Sx based on SyThe absorbance value for the Standard was 0.625 and [FeSCN^ 2+ ] std is 2.00E 4M Calculate the [FeSCN^ 2+ ] in the equilibrium mixture, report the answer to the correct significant figures. The absorbance of the equilibrium solution was 0.451A standard curve for glucose analysis was prepared.The slope (m) was found to be 1.341 while the y-intercept (b) was -0.333. Calculate the concentration (x) of glucose having an absorbance (y) of 0.151. 0.067 0.361 0.858 0.136
- Q) My water hardness experiment is wrong? I did hard water, tap water, and soft water experiment. I mixed hard / soft / tap water 5ml + pH buffer 1ml + 3 drops of indicator + EDTA x ml My expectation was, Hard water will need most EDTA, then tap water, then soft water. However, my experiment result was EDTA of hard water : 0.15ml EDTA of tap water : 0.33ml EDTA of soft water : 0.03ml Also, when I mixed soft water 5ml + + pH buffer 1ml + 3 drops of indicator ; without EDTA, it was already purple color. I tried this for 4 time to make color pink, but I couldn't. The number 0.03ml is ml to change 'purple to blue'. Q1) My result of each water's EDTA ml is reasonable? Q2) soft water without EDTA color can be purple? Thank you.4. determine the amount in mg of the amount of Ag present from ICP mass digested: 1.0821g/L dilution of 10ml stock solution to 100ml volumetric flask X=0.98 (intensity)A student combines Fe(NO3)3 solution and KSCN solution to produce a solution in which the initial concentrations of Fe3+(aq) and SCN–(aq) are both 4 × 10–2 M. The chemical equilibrium forms FeSCN2+(aq): Fe3+ + SCN- <=> FeSCN2+ The absorbance of this solution (from FeSCN2+) is measured as 0.235, and Beer's law equation (the trend line from best fitting) as Abs = 243 x Concentration of FeSCN2+ + 0.012 Determine the equilibrium concentration for FeSCN2+ in mol/L.
- 1 mL was taken from the sample filtrate and mixed with 13 mL pure water and 4 mL sulfomolybdic acid and 2 mL dilute SnCI2 solution by adding it, and after waiting for 15 minutes, the absorbance of the resulting solutions against pure water was read at 520 nm. if the function of the calibration graph obtained with standard phosphorus solutions of 0.5-2.5 mg/mL is y= 0.245x + 0.107 and the absorbance of the serum sample is 0.342, how many grams of phosphorus is the amount in the 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…