Design an effective synthesis for each of the following amino acids starting from the compounds shown...
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents (14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
4. Synthesis. You may use benzene (that is the starting material for a), any organic reagents that contribute four or fewer carbon atoms to the final product, and any inorganic reagents OH OH HN NH 4. Synthesis. You may use benzene (that is the starting material for a), any organic reagents that contribute four or fewer carbon atoms to the final product, and any inorganic reagents OH OH HN NH
On a separate single sheet of paper, do two of the following three syntheses starting from the compound on the left, any other monofunctional organic compounds of four carbons or less, and any other needed inorganic reagents. Once you have completed this problem, take a clear readable image of your work as a single jpg, tif, or pdf file) and upload it using the button below the problem. Make sure to upload your file before expiration of the time period...
Part IV - Multistep Synthesis [14 marks] A. Propose a synthesis of compound A starting from dimethyl malonate. When choosing your synthetic steps, you can use any hydrocarbon with three or fewer carbon atoms, any solvents or inorganic reagents, and any organic reagents that do not contribute carbon atoms to the carbon skeleton in the product. Clearly show the required reagents and the product of each step. You do not need to show mechanistic (curved) arrows. [6 marks] Dimethyl malonate...
Draw the complete synthesis of the compounds Question 44 (10 points) Pick One! Draw the complete, detailed synthesis of one of the three compounds below on your paper. You may use benzene, cyclohexane, or cyclohexanone as one of your starting compounds. You can use any monofunctional organic compound with one or two carbons. You can use any inorganic reagents of your choice. Up to 3 points will be awarded for each additional synthesis problem done correctly. (10 points) < Paragraph...
Devise a synthesis of the following compound using the given compounds (you may use each one more than once if needed). You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials.
Using propyne (structure shown) as your only source of carbon atoms, design a synthesis of the target molecule. You may use any organic or inorganic reagents you choose, but all the carbon atoms in the target must have come from propyne originally. Show the product of each step and the reagents needed for each step. Assume you have an unlimited supply of propyne.
Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. If equal mixtures are anticipated (i.e. ortho / para products) then indicate where separations are needed. NO MECHANISMS! [6 points 2. Give a...
3) Devise a synthesis of the following compound using the given compounds (you may use each one more than once if needed). You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials. Hint: this synthesis will require you to use ozonolysis and a reaction that starts with the letter DI
6. (18 points total) Synthesis: Devise a synthesis of the following compound from the given starting materials. You may use any other organic or inorganic reagents you deem necessary but you must use the given starting materials as your only source of carbon in the final compound OH several steps OH MeOH HO