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- How would you synthesize the products from the given reactants in the followingreactions? Show the reaction schemes and products of each step. No mechanism isrequired.Provide reagents/conditions to accomplish the following transformations. Label each reaction type in the steps you provide. OEt MeO OMeFor eaach image, predict the MAJOR product(s). Show stereochemistry where applicable and draw out ALL stereoisomers formed (as major products) in each reaction. State the mechanism(s) by which the major product(s) are formed (SN1, SN2, E1, and/or E2). Reagents are NOT present in excess.
- Draw reaction mechanisms with all reactants, arrows, intermediates, and products. Your mechanism must account for all the products if more than one product is formed. 4-methycyclohexanol with phosphoric acid H3PO4 to for 1-methycyclohexene, 3- methylcyclohexene and 4-methycyclohexeneWhen 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. PhosgeneSynthesize the following compound from cyclohexanone and any other organic and inorganic reagents you need.
- Propose a synthesis of molecule B from molecule A. For each step, indicate the necessary reagents.Provide major product and a mechanism for each belowFor each reaction, predict what mechanism will account for the major product(s) formed and write (SN1, SN2, or NR) in the boxes provided. Explanations or drawings are not required.
- Please devise syntheses of the product compounds below from their respective starting materials. Each of the synthesis will require multiple steps.Predict the product(s) and provide the complete mechanism for each reaction below.synthesize the following compound given the starting material. Show all the steps, reagents and mechanisms. Do not skip anything. TAKE INTO ACCOUNT THE SHOWN STEREOCHEMISTRY