Provide the structure of the epoxide intermediate and diol final products for each reaction sequence below carefully depict the stereochemistry of each compound Label each epoxide and diol compound as either chiral or archiral. Propose a synthetic to prepare of two or three steps and include both the intermediate compounds as well as the reaction conditions for each step. Provide the optimal alcohol and starting to prepare the product below via the Willamson either synthesis. Propose synthetic schemes (many involve multiple steps) to prepare the alcohol and Provide the optimal alcohol and starting to prepare the product below via the Wiiliamson either synthesis. Propose synthetic schemes (many involve multiple steps) to prepare the alcohol and from starting materials. Provide the arrow pushing mechanism for the reaction below. Explicitly include all non-bonding pairs of electrons and formal charges. Draw the three-dimensional representation of the transition state C-
