A spectrophotometric method for the quantitative analysis of Pb2+ in blood has a normal calibration curve for which Sstd=(0.296 ppb−1)×Cstd+0.003. What is the concentration of Pb2+ in a sample of blood if Ssamp is 0.397?
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A spectrophotometric method for the quantitative analysis of Pb2+ in blood has a normal calibration curve for which Sstd=(0.296 ppb−1)×Cstd+0.003. What is the concentration of Pb2+ in a sample of blood if Ssamp is 0.397?
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- To determine the molar concentration of a metal ion in a solution of unknown concentration, a student fırst made five standard solutions that contain the metal ion of interest and measured the absorbance of each solution in a spectrophotometer at its Amax- A calibration curve was obtained that had an equation of y = 5.747 x + 0.013 Next, the student pipetted 15.0 mL of the initial solution of unknown concentration into a 100.0 mL volumetric flask, and filled the flask with deionized water to the line. The absorbance of this final diluted solution was found to be A = 0.226 at Amax. The color of the original and diluted solution was blue. What is the molarity of the original solution, as well as an approximate Amax for this metal ion? 2max = 599 nm and concentration is 0.247 M Amax 457 nm and concentration is 0.247 M %3D 2 max = 457 nm and concentration is 0.0371 M 1 max 599 nm and concentration is 0.0371 M Amax = 599 nm and concentration is 0.00557 MThe absorbance of an unknown dye solution is measured to be 0.47 by a spectrometer. The linear equation of the spectrometer's calibration plot is y= 2156.5 x +0.0213, where y represents absorbance and x represents concentrations of dye. What is the molar concentration of the unknown sample (in mole L)? O2.08e4 O 2.08e-4 0 125e3 0 125e-3The standard curve was made by spectrophotographic analysis of equilibrated iron(III) thiocyanate solutions of known concentration. You are asked to analyze a Fe(SCN)2+ solution with an unknown concentration and an absorbance value of 0.392. The slope-intercept form of the equation of the line is y = 4538.1x +0.0077. The unknown was analyzed on the same instrument as the standard curve solutions at the same temperature. What is the Fe³+ concentration of the unknown solution? [Fe³+] = mol/L Absorbance Iron(III) thiocynate standard curve 1.0 V 0.5 0.0001 Fe³+ concentration (M) 0 0.0002
- A student prepared four standard solutions of (NH4)2Fe(SO4)2 and measured their absorbance at 505 nm. She created a calibration plot with the best-fit line of y = 9372 x + 0.0539. She measured the absorbance of her diluted unknown sample solution as (4.69x10^-1) nm. If she prepared her diluted sample solution by diluting 10.00 mL of the original solution to a total volume of 50.00 mL with deionized water, what is the concentration of Fe2+ in her original solution? Answer in units of M. Note: Your answer is assumed to be reduced to the highest power possible.(a) For use in an iodine titration, you prepare a solution from 0.222 2 (+0.000 2) g of KIO3 [FM 214.001 0 (+0.000 9)] in 50.00 (+0.05) mL. Find the molarity and its uncertainty with an appropriate number of significant figures. (b) Would your answer be affected significantly if the reagent were only 99.9% pure?A controversy broke out as a dead body was found in a bar on Cornelia Street. The media revealed that minutes before the person died, he described his drink as something stronger than other drinks in the bar. You were the analyst tasked to verify the cause of death. Preliminary qualitative tests showed the possible presence of cyanide in the victim's death. Thus, you tried to quantitatively detect cyanide ions in the victim's drink using spectrophotometric analysis. Standard solutions were of different CN- concentrations were made as shown in Table 2. A 25.0mL aliquot of each standard solution was added with Fe(NO3)3 to form the colored complex, [Fe(CN)6]³ (aq). Each standard solution was then diluted to a total volume of 50.0 mL. The absorbances of the diluted standard solutions were recorded using 1.00-cm cells and at Amax = 725 nm and found in Table 2. Table 2. Raw absorbance measurements for each standard solution of CN-. [CN-] prior to dilution, M Abs@725nm 0.002 0.000 0.040 0.160…
- A 10.00 mL of natural water sample containing Ni2+ was pipetted into a volumetric flask and diluted to 50.00 mL with pure water. In the second 10.00 mL of natural water sample transferred into a volumetric flask, exactly 4.00 mL of a Ni2+ solution with a concentration of 5.99 mg/L was added and then diluted to 50.00 mL with pure water. The measured absorbance is A1= 0.436 and A2 = 0.663. What is the Ni2+ concentration in unit of mg/L in the natural water sample?Blue Blue dye stock solution 0.293 M Absorbance at 630 nm 0.00265 Calibration curve y = 0.0833x A solution is prepared by diluting 2.81 mL of the blue dye stock solution to 25.00 mL. The measure absorbance for the prepared solution is listed in the data table. (a) What is the theoretical molar concentration? [Blue]theoretical | × 10 |M (b) What is the experimental molar concentration? [Bluelexperimental x 10 M (c) What is the percent error? Percent error (blue) =The glucose content of samples can be determined using Nelson’s test. The equation of the line for the standard curve prepared for varying concentrations of glucose is y = 3.0x + 0.2. Based on this information, determine the glucose concentration (in M) of a mango preserve having an absorbance reading of 0.891.
- You begin preparation of the calibration curve to measure absorbance vs concentration of FeSCN2+. To do so, you add 2.422 mL of 0.200 M Fe(NO3)3 to a cuvette and then directly add 215 µL of 0.001 M KSCN. What is the resulting concentration of FeSCN2*, assuming complete conversion of SCN' to FeSCN2+? Enter your answer in units of mM to four digits after the decimal.Many ions form colored solutions when dissolved in water. For example, aqueous Cu2+ solutions are light blue and aqueous Ni2+ solutions look light green. These metals in particularare often found in stainless steel. Would you expect their presence in your samples to interfere in the spectrophotometric analysis of permanganate at 525 nm? Why or why not? I think the answer is that I would expect the Cu2+ in my samples to interfere but not Ni2+ because the Ni2+ is green, signifying a higher wave length that the spectrometer wouldn't be able to pick up on because it was only set to 525 (blue-ish) where as the green is 530-ish. I just want to make sure thanks!Example: You wish to prepare a calibration curve for the spectrophotometric determination of permanganate. You have a stock 0.100 M solution of KMnO4 and a series of 100 mL volumetric flasks. What volumes of the stock solution will you have to pipet into the flasks to prepare standards of 1.00 x10³, 2.00 x10-³, 5.00 x103, and 10.0 x103 M KMnO4 solutions? Solution: for 1.00 x10-³ 0.1 (M1X V1)conc. = (M2 X V2) dil mmol |x V1 = 1.0 × 10-3 -) x 100 (ml) mL mmoly mL V₁= 1.0 mL stock solution. Take home work for the 2.00 x10-3, 5.00 x10³, and 10.0 x10-³ M.