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- Devise a synthesis of compund 1 starting from ethyl acetoacetate. You should include details of all reagents used and provide a mechanism for each step.select the most appropriate reagent(s) to effect the change. 1. Disiamylborane, 2. HO–, H2O, H2O2 H2, Pd K2Cr2O7, H+ NaOCl H2SO4, HgSO4select the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO4
- Which reagents would you use to perform reaction B?a) PBr3.b) p-toluenesulfonyl chloride.c) SOCl2.d) NaOCl, NaOHWhat alkyl halides are needed to prepare each carboxylic acid using the malonic ester synthesis?plese quickly thanks ! 4. Please write out the equation to the synthesis of Ethyl Acetate. Since this reaction is reversible, how to drive an esterification toward completion. How to work up after the reaction completion and explain the use for every workup.
- Show a complete mechanism for the meta-bromination of nitrobenzene (PhNO2) using Br2/FeBr3 to give meta-bromonitrobenzene. Use resonance forms to explain why nitrobenzene directs meta.Propose an efficient synthesis for the following transformations using ONLY acetoacetic ester synthesis. R1 and R2 are the alkyl groups that should be added to the alpha carbon labeled in one of the attached image.Show how the following compound can be prepared by a malonic or acetoacetic ester synthesis (or other B-dicarbonyl) reaction:
- Show how to synthesize the following compound using either the malonic ester synthesis or the acetoacetic ester synthesis. Q.) Cyclopropanecarboxylic aciddraw out the reactions for synthesis of 2,6 dinitroaniline. show the necessary reagents used in the reaction.?Propose a mechanism for the followingreaction → NaOH,acetone
