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Question 1: Two chromatographic columns (GC) are being compared for use in an analysis. One is a 50 cm long packed column that is 5 mm in inside diameter (ID), with a stationary phase that is 1um thick on the support packing and has a total of 25,000 theoretical plates. The other column is 1 meter long, also 5 mm ID, with the same thickness of stationary phase on the support, and has 40,000 theoretical plates. Ignoring any other variables:
a) Which column would provide the best separation of sample peaks? Why?b) Which column would provide the sharpest peaks? Why?c)If the 50 cm column had a stationary phase thickness of 2 um on the support, how would that affect the results? (Hint-"C" factor of Van Deemter Eq.)
Question 2: The use of an FTIR Transducer has never become commonly used as a detector for HPLC because?
Question 3: In High Resolution Carbon NMR Spectroscopy, the phenomenon of "Spin-Spin Coupling" is rarely seen and, if seen, is very minor. Very briefly, why is this true?
Show all the steps in the mechanism for the following reaction, When benzene is mixed with deuterated sulfuric acid, deuterium is slowly incorporated onto the ring. Show the mechanism for this reaction and explain how this relates the sulfonation of ..
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