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You need a graphic concentration versus absorbance.
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patients absorbance/absorbance of the standard*concentration of the standard gives you the glucose concentration of the patients sample
Absorbance rises with concentration because there is more material for a given frequency of light to be absorbed in. Your statement is false.
Beer's law says that absorbance is directly proportional to concentration. So if there is zero concentration there should be zero absorbance (0,0).
Because in high concentrations you will have scattering, multi event absorbance, and self-absorbance which are mostly non-linear effects and are not described by the Beer's law.
The absorbance depends on the concentration of the chemical species to be analyzed (for identic spectrophotometric cells).
Absorbance refers to a measure of the capacity associated with a substance as regards absorption of light of a specified wavelength. Whenever you plot a graph of absorbance vs. concentration a direct relationship should be produced
The slope of absorbance vs concentration reptresents the value of εb, where ε is the absorbtivity with units of (L/mol cm) and b is path length measured in cm.
The absorbance data correlates to the initial protein concentration in ug ml in one way. It breaks down protein in the stomach by the action of the stomach acid.
Depends on the length the light traveled through the solution and the solution concentration. molar absorption = absorbance/(length x concentration) length is typically in cm and concentration is typically in mol/L
you would have to know the following values, Absorbance (A), Concentration (C), and cell length (l) and plug it into the formula A=eCl or C = A/Cl