Suppose I dissolve a small particle of PABA in methanol and run the solution produced in UV-Visible spectrophotometer at 200-400nm. I will get a absorbance vs. wavelength spectrum. There is no way I can construct a logarithm epsilon vs. wavelength spectrum in this situation.
On the other hand, if I run a solution of 10-6M PABA solution, I will still get a absorbance vs. wavelength spectrum but I can construct a logarithm epsilon vs. wavelength spectrum by changing the absorbance scale to log(absorbance/10-6) scale.
Did I got this, or have I made a mistake?