a. (2 points) In Question 3, you were asked to consider the monohalogenation of an organic compound. Based on the structure shown below, predict the major monobromination product. If the reaction yields a chiral product, utilize appropriate dashes or wedges to indicate any specific stereoconfiguration of the product. If the reaction should yield a racemic mixture, indicate this by drawing either enantiomer and appending the notation (rac) next to it. If diastereomers are possible, draw all diastereomers. Br2 hv (assume monobrom ination) b. (4 points) If the monobromination process creates a racemic mixture, explain why. If the monobromination process does not create a racemic mixture, explain why not in two sentences or fewer. (4 points) Illustrate your explanation in part b by drawing the relevant free radical intermediate being careful to show relevant 3D geometry. NT: A Newman projection is a great idea! c.