Show the organic product formed when methyl propanoate is reacted with lithium sopropyl amide, then methyl ethanoate is slowly added to the mixture. The mixture
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Solved in 2 steps with 2 images
- Show a complete arrow pushing reaction mechanism for the reaction below.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.Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures. 1st pic-Please identify the acetal and hemiacetal in your mechanism. 2nd pic- Show how you would synthesize the starting ylide.
- answer all of them please, thank you. Complete the following reactions in sequential order. Show the product after each step and put a box around the final productshow the missing reagents and intermediates in the reaction sequence belowCan someone please explain to me how to find which reagents are appropriate for the first image along with the end product and for the second image, how would I go about drawing the mechanism?
- please show full and complete pushing arrow mechanisms. Write the full mechanism and complete with the corresponding reactants and productsAlcohols react with sulfonyl chlorides to form sulfonate esters. Only the O-H bond of the alcohol is broken in the reaction, and so no inversion of configuration occurs. The resulting sulfonate esters are reactive in SN1 and SN2 reactions since the sulfonate group is a very weak base and is therefore a good leaving group.Draw curved arrows to show the movement of electrons in this step of the 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.