4) Draw the major product(s) of each reaction. Be sure to indicate relevant stereochemistry. 5) Determine the absolute configuration of the electrophilic carbon in the starting material and in each product. 6) Are your answers above consistent with a. Protonation of a secondary alcohol goes through a carbocation intermediate and subsequent rearrangement after loss of the leaving group (S 1 mechanism)? b. The two-step process of 1) tosylation followed by addition of 2) Nal, results in an overall inversion of configuration? c. The two-step process of 1) chlorination followed by addition of 2) Nal, does NOT result in an overall inversion of configuration