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- 3) Propose a mechanism for the following reaction. HO H2SO4Predict the major product of the following reaction and draw it in the space provided. 1) NAOMe Br 2) Meo Ome Br 3) NaOt-Bu 4) HCI, H₂O, heatPredict the structure of compounds A and B and provide a mechanism for the reaction. OH CI HOO A H3O*
- Provide 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 OHPlease give a detailed stepwise mechanism for the following reactions. All arrows, charges, and intermediates must be shown. 1) CN H*, H₂O, heat Яон OHEthylene oxide is the starting material for the synthesis of 1,4-dioxane. Propose a mechanism for each step in this synthesis.
- Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.7. Provide the synthesis for the following product starting with the provide starting material. More than one step is required. Show the mechanism for each reaction. CI- Cl- Starting Material Productprovide a mechanism which explains the following conversion OH ist NaOH H₂O