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- Show the retrosynthetic analysis and forward synthesis of the following compounds. 1. د c 2. OCH3Q6 Complete the retrosynthetic analysis. Supply all reagents and precursors, for both parts: A and B. Fewest possible reaction paths should be choiun. Part A V Part B MiWrite a Retrosynthesis and a foward synthesis.
- Show reasonable mechanisms for the following reaction.Provide the retrosynthetic analysis and synthetic route for the following Compound.To preview image click here ↓ Perform the retrosynthetic analysis for the indicated bond and choose the correct synthetic equivalents. A. B. O A B D : OMe + :0: + NaOMe + NaOMe C. D. MeO +ÖMe + NaOH NaOH
- 1. Please provide the synthesis scheme for the first proposed synthesis route. 2. Provide the synthesis scheme for the second proposed synthesis.Spasmolytol, as its name suggests, is an antispasmodic. Given this retrosynthetic analysis, propose a synthesis for spasmolytol from salicylic acid, ethylene oxide, and diethylamine. Br. NEto OH OCH3 ОН Br Spasmolytol Salicyclic acidRetrosynthesis. Show how the following multi step chemical transformation can take place. Provide reagents for each step in the synthesis, Include structures of intermediate products. Do not provide a mechanism or curved arrows. Be neat and clear! Note any special instructions. Design a synthesis starting from benzene, a. b. c.
