For the last step in your potential Nobel-prize winning cancercure drug you need 3-cyclopentyl-1-phenylhexan-3-ol, but nochemical company sells this particular alcohol. You, being thewonderful synthetic chemist that you are, figure you can make thistertiary alcohol from the simple Grignard reagent reaction youlearned in your CH223 course.

A) Draw the structure of your target alcohol. Use the nameto make sure you have the correct number of carbons:

B) If the Grignard reagent contains the aromatic ring, draw boththe appropriate Grignard reagent and carbonyl compound(not an ester) you would need to make your targetmolecule. Input the Grignard reagent first, then click the \"New\"tool to allow the carbonyl compound input.

C) If the Grignard reagent contains the five-membered ring, drawboth the appropriate Grignard reagent and carbonyl compound(not an ester) you would need to make your targetmolecule. Input the Grignard reagent first, then click the \"New\"tool to allow the carbonyl compound input.


D) There is one more combination that you could use to arrive atthe targent alcohol. Input the Grignard reagent first, then clickthe \"New\" tool to allow the carbonyl compound (notan ester) input of this last possible synthetic scheme.