The nucleophilic addition reaction depicted below involves a prochiral ketone carbon atom reacting with a nucleophilic hydride ion source (LiAlH4 or NaBH4) and, subsequently, a proton source (e. g., H2O or dilute aq. HCl). Consequently, the reaction produces a racemic mixture of an alcohol. Finish drawing the structures of the products resulting from nucleophilic attack upon the front and back faces of the carbonyl group, being careful to specify the stereochemistry via wedge-and-dash bonds.