4. 5. 6. H₂C H₂C H₂ =0 H₂ ol CN DIBAL 1 eq NaBH4 Br Synthesize the compound below starting from benzene, alcohols of four carbons or fewer, and any inorganic reagents. NHCH₂CH3 LIAIH4 CH3

Topic: Review of Organic Synthesis: Access the attached document, and determine the final product of these organic synthesis reactions. To make things easier, the product for all three syntheses is the same, but I just want to provide the appreciation that there are sometimes multiple ways to get to the same synthetic product. For each pathway, show the intermediates between the arrows by redrawing, and attaching of course, each pathway. In addition to the attachment, be sure to describe what is going in in the text box window of the discussion. For ease, label your descriptions A, B, and C for each of the three reactions that yield the same organic synthesis product.  Finally, comment on the final product in terms of the expected IR peaks that can help in identification of the synthetic product. How would these IR peaks generated by the product be different than the IR peaks generated by the reactant, had the synthesis not taken place? Be as specific as possible... determine which…

answer questions 3 & 4 and all parts!! will be rating!!

In each reaction box, place the best reagent and conditions from the list. 1) CEN 2) 3) 4) 5) Answer Bank NANH, NaBH, acetone CH,CH, MgBr (excess) acetic acid acetate ion CH,OH, H,O* (cat.) LIAIH, (CH,),CHMgBr (excess) CH,MgBr (excess) H,0 H,0*, H,0, heat acetyl chloride