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The specific rotation of (S)-(+)-2-octanol is +89o . What is the enantiomeric excess (as a percentage), and of which isomer, for a sample of 2-octanol whose measured specific rotation is +59o?
For the first part I know the excess is 66% the question I need help with is the second part below.
This 2-octanol sample was the product of a solvolysis reaction that started with pure (R)-2-bromooctane. Predict the optical activity of the 2-octanol product if the reaction proceeded a) by SN2 and b) by SN1 mechanism. How do you explain the observed optical activity?
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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