3. Using ethanol and any compound with 1 or fewer carbons, the product shown below. (7.5)...
5. Using the starting material and any compound with 1 or fewer carbons, synthesize the product shown below. (2.0) Zb starting material on a manner AOH starting material OR
Please show your work thanks Snow how to prepare the product shown below, using only ethane as the source of carbon. You can reagent that is needed to accomplish the synthesis, but the final carbons in the compound must nav , but the final carbons in the compound must have come from etnane. Use retrosynthesis analysis and the special arrow) to work backwards to the starting material mnen, show the complete sequence using the "regular" reaction arrow. (Note (hint) that...
Propose a simple synthesis for the compound shown below, using the provided starting material and any organic or inorganic Reagent. Draw all intermediates. (Use alkene and alkyne reactions)
b. Complete the synthesis shown below using any reagents of four carbons or fewer. (Consider: Robinson) [6 points]
2) Devise a synthesis of the following compound using only ethanol. You may also use any needed Inorganic or organic reagents but all of the carbons in the target molecule must come from ethanol. Hint: this synthesis will require you to use a Claisen reaction
Please explain the mechanisms! 1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Multiple steps are required. The number of steps you use does not matter. Reactions should give the desired product as a major product. For full credit show the product of each step (reaction). If you make use of organometallic reagents such as Grignard, Wittig, organolithium, organosodium, organocopper, etc. you must...
3. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) но
3. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) i =
3. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) HO
5. Outline an organometallic synthesis the compound below starting from cyclohexanol and alcohols of 3 carbons or fewer using any necessary solvents and inorganic reagents. (5pts)