=> (8 pts) Use retrosynthetic analysis (that is, use retrosynthetic arrows as was done in class) to suggest a synthesis route for the transformation shown below. Sear bons
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- help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all workingWhen phosgene is treated with excess methanol, a product is formed whose "H NMR spectrum shows one peak-a singlet at 3.8 ppm. Provide a complete, CH,OH ? CI CI detailed mechanism for this reaction. PhosgenePropose a synthetic route to perform the next transformation.
- a) Show the structure of the reagent needed for this transformation and the mechanism for its synthesis using Ph3P and BuLi. ? CH₂ b) Show the mechanism for the reaction in (a) using the reagent that you provided.Fraw the lower and higher molecular weightPropose a synthesis from benzene and show each intermediate
- Provide an arrow pushing mechanism for the following reaction. Include protons and each step clearly indicated. CI NaOMe CH3 МеO O.Propose a multistep synthetic route to the following structure that includes all reagents, substrates, as well as the products in each step.. Provide a mechanism for the following reaction. H cat. HO HO H₂O OH O-H T →