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Q: Propose an efficient synthesis
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5. Propose a synthesis.
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- Propose an efficient synthesis N.Y Part B Identify which reagent should be used to form the following product: View Available Hint(s) 1. mCPBA. 2. H₂O, H₂SO, O H₂O, H₂SO, 1. Os0₁. 2. NaHSO O1 Hg(OAca), H₂O. 2. NaBH. Submit Y ? WSynthesis - 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 search
- 1. Provide the mechanism. NaOEt EtOH CO₂EtIdentify compounds A-G in the following synthesis scheme. 1. Cl, (excess), NAOH A 2. H2О, НС CI SOCI, C В AICI3 Same as above 1. LIAIH4, Et,0 F 2. H,O, NH,CI conc HNO3 1. HCI, Fe D 2. NaOH E Pyridine GMechanism 5. Propose a mechanism that accounts for the transformation below. [5 pts] TIOH (cat.) HO aq. acetone Me mechanism:
- Identify compounds A-I in the following synthesis scheme. CUCN D conc HNO3 1. HCI, Fe NaNO2 A 2. NaOH В HCI Same as above Br2 Mg(s). F Et,0 1. D NaBH4 1. NaH >E FeBr3 G ELOH 2. H2О (еxcess), H,SO4 2. C6H5CH,Brwrite mechanism ? CN O H 1. HO. OH H+ (1 equiv.) 2. a) LIAIH4 b) H₂O work-up 3. H+3. Propose how to make the following alkene through a Wittig synthesis. Include the synthesis of the ylide and all arrow pushing. oh