5) Show a reasonable synthesis for the following reaction. The reaction can be completed in 3 steps. Draw a reasonable (and complete) mechanism for the first transformation and the last transformation. Name the type of reactions for each step. HO OH OH CHO
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- Show the organic product formed when methyl propanoate is reacted with lithium diisopropyl amide, then methyl butanoate is slowly added to the mixture. The mixture is neutralized with aqueous acid to obtain a neutral product. Show the steps in the mechanism as reactant is converted to final product. show appropriate arrow pushing and any charges, and draw a box around the final product.show full mechanism.Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.
- Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. 1) CH3CH2M9B CH3OH H+ (ехcess) но 2) H30*, H2O B A OCH3The following transformation can be accomplished by reactions we have studied in this chapter and Chapter 20. Name the type of reaction used in each step.2) reaction sequences to carry out those transformations. Draw the expected product of each step proposed. Substantial partial credit can be obtained for incomplete or incorrect answers. You may present your solutions on the following blank page if you need the the following reaction transformations, and propose room. H3C CH, H3C CH3 of HN- -NH HO,C Co,H но H,C CH3 CEN OCH3 OCH3
- Complete the mechanism for the given reaction of 2‑butanone in methanethiol and acid by adding any missing atoms, bonds, charges, nonbonding electrons, and curved arrows. Select the name that best describes the final product.2) Complete the mechanism for the following reactions. Show the formation of all products. A) B) H Br Br 1) H₂PO4 -OH 2) Nabr LOH H₂O Кон он -Br & +Propose an efficient multistep synthesis for the transformation shown below. There is no need to show the mechanism of any step, only the reagents required for each step, and the resulting intermediate product of each step. 1ouborq sto vino noib restriction: The given reactant is your only source of carbon atoms, but you may use more than one molecule of the reactant. multiple steps + en. OaT