1. For each compound drawn below: (a) Label each OH, Br, and CH3 group as axial or equatorial. (3 pts) (b) Classify each conformer as cis or trans. (3 pts) (c) Translate each structure into a representation with a hexagon for the six- membered ring, and wedges and dashes for groups above and below the ring. (4.5 pts) (d) Draw the second possible chair conformation for each compound and lab each OH, Br, and CH3 group as axial or equatorial. (7.5 pts) (e) Looking at conformer (1) that was given to you and its corresponding ring flipped conformer you drew in 1(d), identify which structure is the most stable and explain your reasoning? (4 pts) OH HO CH3 Br OH OH