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- Show the retrosynthetic analysis and foreward reaction of the following compounds. Please draw out the structures too.Show the retrosynthetic analysis and foreward reaction of the following compounds. Please draw out the structures too. довь5. Provide an efficient synthesis for the following transformation. Synthesis with the fewest steps, best yields and best selectivity will get maximum marks. Me,SiQ
- Please give me the reagents and show the mechanism. Thank you so much.3. Propose an appropriate synthetic route by retrosynthetic analysis for the following. Show all work including arrows, electros, Solvent, etcQ6 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 Mi
- Perform a retrosynthetic analysis of the below including all necessary steps and reagents.20:33 1 : ●●● all the proper notations for depicting resonance. 4. Provide the full mechanism (curved arrows and intermediates) that leads to the product in the scheme below. Draw the structure of the product to help you see how the starting materials will combine. Use that as a clue to figure out how to draw the mechanism arrows. ccare in your scheme. Be sure to use NaOEt 00 i 5. Provide the major organic product of the reaction shown. Determine if these conditions are best for SN2, SN1, E2, or E1. Be sure to indicate stereochemistry by using the proper wedges/dashes in the product. acetone phenyl butanoate Send a chat ODo a retrosynthetic analysis on each of the following compounds, ending with available starting materials.