Most analytical machines used in science can either measure absorbance of light, like the spectrophotometers used in BioZ 151 and 152 labs, or can measure change in electrical conductance. In order to convert things like absorbance values into concentration data, a linear regression is used. In order to determine nitrite concentration in water samples, nitrite is reacted with several chemicals to produce a purple color. The absorbance of the solution is measured from known amounts of nitrite to produce a standard curve to analyze samples. Use the data in the provided table, or from the linked spreadsheet to make a graph and perform a linear regression using treadline. mg/L NO3- Absorbance 0 0 0.1 0.183 0.3 0.542 0.5 0.914 0.7 1.298 1 1.61 In order for this to work, samples must be diluted prior to measurement so that the concentration falls within the range of the standard curve. If a sample underwent a 0.05 dilution, and produce an absorbance value of 0.48, what is the resultant concentration of NO2- in mg per L? Report your answer to two decimal places. Tip: The regression equation will give you the final concentration. The dilution is equal to V1/V2. The question is asking for the initial concentration.
From Linear Graph
Slope=1.6231
Intercept= 0.0654
From regression equation, Y=mx+C, Y=unknown absorbance, m=slope, x=unknown concentration, C=Intercept
for unknown absorbance (0.48) concentration obtained is 0.26 mg/L
Initial Concentration=.0.26 mg/L *× Dilution Factor
=0.26* 0.05
Answer= 0.013 mg/L
Most analytical machines used in science can either measure absorbance of light, like the spectrophotometers used...
Please answer #2. I'm unsure how its done
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Page 10 Beer's Law Akuch Pyrs to shes your werk Show your work, Aplications Attach Peyes 27, what is the value of absorbance that corresponds to 35.0 %T? 28. Molar absorpt ivity is the absorptivity when concentration is in units of molarity and the gth is in centimeters. If a 1.53 x 10 M solution has an absorbance of 0.426 in a 1.00 em cell when measured at a wavelength of 254 nm, what is the molar absorptivity of the...
lab question 1. What is the basis of the different purification methods? 2. What are some of the factors the might have interfered with your results? 3. How might you improve the process to increase the yield and purity? lab process E. coli BL21 (DE3) cells were transformed with the pET Topo-1521 vector containing a reading frame encoding the green fluorescent protein (GFP). Cells were cultured in M9ZB media at 37°C until the absorbance at 600 nm reached 0.7, at...
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