1. COMB 2. wwerd 6. Propose multi step synthetic routes from the given organic molecule to the indicated product. Y...
nob 2. Strong acids always protonate amide oxygens and never protonate amide nitrogens. Provide two reasons that explain this fact (4 points). 6. Propose multi step synthetic routes from the given organic molecule to the indicated product. You can use any organic solvent and any of the following organic chemicals CH,-, CH,CH,-Br and inorganic chemicals: co, KCN, Mg, Li, Cul, Zn, Sn, HCI, H,O, H,SO, DIBALH, LIAIH, NaBH, Cro, H, and Pd catalyst, PBr, and SOCI,. (24 points, 6 each)....
Do all work on this paper. 1. The compound below on the left has a much higher melting point than its isomer on the right. Explain. (4 points) Tronohon o llottobu 2. Strong acids always protonate amide oxygens and never protonate amide nitrogens. Provide two reasons that explain this fact (4 points). 3. Draw the complete mechanism of the reaction below and indicate the location of "O in the product. (6 points). CH, + 1 equivalent of KOH in water...