Need help on the following please. You are provided sample solutions containing the following compounds, but in each case, there is some unknown interference that prevents you from making accurate absorbance measurements at their optimal wavelengths (Amax). [Recall that thedefault wavelength in the simulation (the "preset" wavelength) corresponds to Amax, as discussed above.]Use the variable radio button in the simulation to identify whether there are any other wavelengths that correspond to local maxima such that they could be used to determine concentration, then complete the diagram below by labeling thealternative wavelength (if any) for each molecule. It is easiest to see changes in the absorbance when you use a high analyte concentration.Drag the appropriate alternative wavelengths to their respective targets. If there are no appropriate wavelength values, drag no additional peaks to that target.• View Available Hint(s)ResetHelpno additionalpeaks380 nm549 nm544 nm392 nm433 nm411 nm.761 nmCo(NO,),K,Cr,O,COCI,K,CrO,NICI,KMNO, Path length and light absorptionWhen light travels longer distances through a solution, it encounters more molecules that could potentially absorb the photons. The path length can often be overlooked in terms of the Beer-Lambert law, and this is because the value is typicallyassumed or estimated based on the dimensions of the container holding the solution. Another reason it is overlooked as an individual value is because calibrations are often performed by plotting absorbance versus concentration for a prepared rangeof concentrations. As a result, the terms e and b are usually combined into a single constant (representing slope).Although absorbance measurements can technically be made between the values of 0.00 to 2.00, the instrument's specifications do not always guarantee accuracy over the entire range because of technical limitations of the detector. A common rangefor economically priced spectrophotometers allows for absorbance measurements with a known tolerance between 0.20 and 1.50. If the concentration is too high for measurement, meaning it produces an absorbance greater than the instrument'sspecification (e.g., 1.50), then the sample can easily be diluted. When the concentration is too low, the options are more limited, but we will explore one of them.Part CVitamin B12 is a protein with a cobalt ion coordinated at its center. You use a standard protein assay to quantify the concentration of the protein in an unknown sample containing the vitamin, and you believe its concentration to be 17 mM. Toconfirm the result, you denature the protein with heat and HCl (a strong acid), then isolate the salt solution that contains CoCl. You intend to use spectroscopy to confirm the concentration of cobalt at a wavelength of 549 nm, but you suspect thatthe sample is too diluted to provide you an accurate value using a standard 1.00 cm cuvette. However, you notice that your spectrophotometer can accommodate larger sized vessels.Use the ruler in the simulation to estimate the minimal path length you would require to obtain an absorbance measurement of at least 0.20 using a wavelength of 549 nm for a concentration of 17 mM (assuming the concentration you measuredusing the assay to be true).Express the path length in centimeters to two decimal places.• View Available Hint(s)?b =cmSubmit

Question

Need help on the following please. You are provided sample solutions containing the following compounds, but in each case, there is some unknown interference that prevents you from making accurate absorbance measurements at their optimal wavelengths (Amax). [Recall that thedefault wavelength in the simulation (the &#34;preset&#34; wavelength) corresponds to Amax, as discussed above.]Use the variable radio button in the simulation to identify whether there are any other wavelengths that correspond to local maxima such that they could be used to determine concentration, then complete the diagram below by labeling thealternative wavelength (if any) for each molecule. It is easiest to see changes in the absorbance when you use a high analyte concentration.Drag the appropriate alternative wavelengths to their respective targets. If there are no appropriate wavelength values, drag no additional peaks to that target.• View Available Hint(s)ResetHelpno additionalpeaks380 nm549 nm544 nm392 nm433 nm411 nm.761 nmCo(NO,),K,Cr,O,COCI,K,CrO,NICI,KMNO, Path length and light absorptionWhen light travels longer distances through a solution, it encounters more molecules that could potentially absorb the photons. The path length can often be overlooked in terms of the Beer-Lambert law, and this is because the value is typicallyassumed or estimated based on the dimensions of the container holding the solution. Another reason it is overlooked as an individual value is because calibrations are often performed by plotting absorbance versus concentration for a prepared rangeof concentrations. As a result, the terms e and b are usually combined into a single constant (representing slope).Although absorbance measurements can technically be made between the values of 0.00 to 2.00, the instrument's specifications do not always guarantee accuracy over the entire range because of technical limitations of the detector. A common rangefor economically priced spectrophotometers allows for absorbance measurements with a known tolerance between 0.20 and 1.50. If the concentration is too high for measurement, meaning it produces an absorbance greater than the instrument'sspecification (e.g., 1.50), then the sample can easily be diluted. When the concentration is too low, the options are more limited, but we will explore one of them.Part CVitamin B12 is a protein with a cobalt ion coordinated at its center. You use a standard protein assay to quantify the concentration of the protein in an unknown sample containing the vitamin, and you believe its concentration to be 17 mM. Toconfirm the result, you denature the protein with heat and HCl (a strong acid), then isolate the salt solution that contains CoCl. You intend to use spectroscopy to confirm the concentration of cobalt at a wavelength of 549 nm, but you suspect thatthe sample is too diluted to provide you an accurate value using a standard 1.00 cm cuvette. However, you notice that your spectrophotometer can accommodate larger sized vessels.Use the ruler in the simulation to estimate the minimal path length you would require to obtain an absorbance measurement of at least 0.20 using a wavelength of 549 nm for a concentration of 17 mM (assuming the concentration you measuredusing the assay to be true).Express the path length in centimeters to two decimal places.• View Available Hint(s)?b =cmSubmit

Accepted Answer

As per Bartle by guideline I am allowed to answer one question at a time.