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- . CONUERT D-LYOSE TO A +HAWTHOAN PROSECTIO (MUST Stlow ALL STEPS): OH Ho.The reaction below is a base-catalyzed aldol reaction. O || CH₂-C-H CH3-C-H Ethanal (Acetaldehyde) H I CH3-C-H Ethanal (Acetaldehyde) NaOH Draw curved arrows to show the movement of electrons in the step of the mechanism shown below. Arrow-pushing Instructions AC⇒x= :O: || :CH₂-C-H OH Bl CH3-CH—CH2-CH -CH₂-1-1 a 3-Hydroxybutanal (B-hydroxyaldehyde; formed as a racemic mixture) :0: :0: || CH3—CH—CH2-C-H A tetrahedral carbonyl addition intermediate XAgCOAO) Prupose everystep a reaction WmechaNsm fur Hhe above showns and intermedirte.
- Draw the products formed when each ester is treated with lithium hydroxide and water. Reaction A Select Draw Rings More CH3CH₂CH(CH3)OC=OCH(CH3)₂ LiOH H₂O |||||| HO 3 Ć H O OH Li Erase Q2QDraw the products formed when A is treated with each reagent: (a) H2 + Pd-C; (b) mCPBA; (c) PCC; (d) CrO3, H2SO4, H2O; (e) Sharpless reagent with (+)-DET.(h) CHCO CI CH3CO2H, 50 °C Draw the major product(s) of the reaction.