Mechanism 8: Consider the reaction below, which yield a single enantiomer of the product. [10 pts] a. propose a mechanistic rationale for the observed transformation. b. based on your mechanism, provide a revised illustration of the product showing the absolute stereochemical configuration of all stereocenters i.e. draw the actual enantiomer that forms c. explain for the fact that only a single stereoisomer forms in the reaction (the red stereoisomers do not form) d. Classify the cyclization according to Baldwin's rules. Br LOH, BOMOH 0C to it "Br BI "Br SAC DAC OAC Br do not form OAG revised product mechanism: explanation