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- A. B. C. D. E. Br Br H H OH Which of these syntheticProvide mechanism with arrows and charges H3CO. NaOH H2OSYNTHESISI Show how the compound below can be synthesized efficiently from benzene, propane, and any necessary reagents. Assume that you can separate ortho and para isomers, if both are formed in any step. NH,
- 1. Provide a detailed mechanism for the following reaction and give the major product. CI AICI 3Give the major substitution product of the following reaction. a O CH3CO₂H Br heat CH₂ ? O There is no reaction under these conditions or the correct product is not listed here.3) Show how you would synthesize the following Compounds, storting with benzene or toluene ond ASSume any necessory pro duct (ond seperoble from ortho) in ortho, pora reogents, poro is the mogor mixture c)o- chlorobenzoic ocid d) m- chloronitro benzene
- Synthesis - Drawing Saved Synthesize the following compound from cyclohexanol, ethanol, and any other needed reagents. он Part 1 out of 2 plnts Preparation of organometallic reagent: еВook Print References A B CH3CH2OH CH3 CH2MGB. draw structure ... Draw the intermediate product above and select the correct reagent for A. O Br, O NaBr O HBr O Select the correct reagent for B. O Mg O MgBr2 O MgI, O MgO Hin Soluti raw 11 e here to searchProvide a mechanism with products for the reaction above. CH3 2Na/Liq.NH₂Provide efficient syntheses of the following compounds using 1-pentene as your starting material and using any other necessary reagents. ? HO ?
- 4) Synthesize the following molecule using the indicated starting material, showing all reagents used in each step. H. from CN H HO EtODraw the major organic substitution product or products for (2R,3S)-2-bromo-3-methylpentane reacting with the given nucleophile. Clearly drawn the stereochemistry, including a wedged bond, a dashed bond and two in-plane bonds at each stereogenic center. Omit any byproducts. Br CH;CH20 (conc.) H.Q12. (1-bromoethyl)benzene 1 udergoes an elimination following an E1 mechanism. Fill in the following synthetic scheme by drawing the structure of intermediate 2 and product 3. The chemical formula of product 3 is provided as guidance. CH; RDS Br C3Hg E1 2 3