Show how you would accomplish each of the following transformations. More than one step may be required. Show all reagents and all intermediate structures. 17 009
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- beginning with the compound shown, suggest a synthesis for each of the compounds shown below. Clearlyshow all intermediates and reaction conditions. Several steps are required for each synthesis conversionPart 2 - Syntheses (64 points in total) Propose a plausible synthesis for each of the following transformations. Write all steps with required reagents and intermediates. As a product, one of the enantiomers is shown only.Provide a detailed step-wise mechanism for the following reaction. Be sure to show all steps, intermediates, formal changes, and show the movement of electrons with curved arrows. You do not need to show transition states.
- Show how you can carry out the following transformations with the limitations given below and any readily available (i. e. existing reagents. If more than one step is required, give reagents and product(s) for each step. Show structures for all the compounds. Reaction mechanisms NOT required Include a protection group on benzene. NH₂ NO2VShow how you would convert 2-methylcyclopentanol to the following products. Any of these products may be used as thereactant in any subsequent part of this problem.(a) 1-methylcyclopentenePlease provide the reagents for the following transformations.
- Complete the reaction schemes below provinding the reagents required to achieve transformation. Note that more than one step may be required.Show how to synthesize the following product as the major product starting with 2,2-dimethylpropane as the starting material. You may use additional reagents and any number of steps. Be sure to list each step with all reactants/reagents/conditions required. (Do not use hydrogenation reactions). Write the process.7. Compound X is an antibacterial drug of the sulfonamide group, and was widely used in the mid-20th century as one of the earliest antimicrobial drugs. X is synthesized through the following sequence of reactions. Draw structures of A-C and X, and show mechanism for the reaction C to X. NO2 NO2 1) NaNO2, H*, H20 H202 NH3 B H2 NaSH > X ZrCl4 Pd 2) O=S=0 H2N `NH2 NH2
- B) Write the most stable enol forms of the following compound, and choose which of them is more stal With explanation. TH1003 al sein) soobel. Xudda0 Jor'larizzA suddz zuddall Jen CH3Provide detailed step-wise mechanism for the following reaction. Be sure to show all intermediates, formal charges, and show the movement of electrons with curved arrows. a 4+H₂Q 044 OHShow how to synthesize the following product as the major product using any reactants/reagents and number of steps. Be sure to list each step with all reactants/reagents/conditions required. (Do not use hydrogenation reactions) Но
