Provide a step-wise synthesis of the molecule shown below using the two starting materials provided and anything else you may need.
Provide a step-wise synthesis of the molecule shown below using the two starting materials provid...
5. Provide a synthesis for each molecule shown below starting from the indicated compound. In addition to the starting material, you may use any necessary reagents. OH a. Eto Et
Provide a stepwise synthesis for the following reaction. you may use the indicated starting materials as well as any organic or inorganic reagents.
5. (12 pts) For the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. OH O from starting materials containing three or fewer carbon atoms from starting materials containing two or fewer carbon atoms
4. (12 pts) For each of the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. HC НОХ H₃C CH весна from propanal as the only carbon source from starting materials containing three or fewer carbon atoms
Design a synthesis for the following molecule starting from commercially available starting materials. You may use any reagents along the way that are commercially available. Should a subtrate you need not be commercially available, then you need to show me how you would synthesize it. Pay close attention that your design takes into account the stereochemistry. ОН НО то он ОН НО
Problem 3 Propose a synthesis of the following molecule from the given starting material. You may use any reactions we have learned in this course so far, and any reagents containing the carbon atoms you need. If you make a mixture in any of the steps, place a box around the compound you would separate from the mixture, and carry on with your synthesis assuming you can isolate the desired regioisomer. NH2
9. P ropose a multi-step synthesis to accomplish the overall transformation shown below (make the molecule on the right starting with the molecule on the left). Show all necessary reagents and products for each forward step. [It is not necessary to show any mechanisms.] OH 10. Propose a multi-step synthesis to accomplish the overall transformation shown below (make the molecule on the right starting with the molecule on the left). Show all necessary reagents and products for each forward step....
3. Design a synthesis of the following molecule starting from benzene and molecules of two or less carbon atoms. You are not limited in your choice of reagents or number of steps. ΝΟ2 ΝΗ2 12 Br 10 Cl CO2H он CI ΝΟ2 ΝΗ2 12 Br 10 Cl CO2H он CI
Provide a multistep synthesis for the desired product using the indicated starting materials. You may use any additional organic or inorganic reagents. Do not draw any curved-arrow mechanisms. The best answ will require nine or fewer steps. OH 었 OET NH2 Starting Materials NH3 OH Desired Product
21. Do Only One! Propose a multistep synthesis using the starting materials shown and any other reagents/reactants you need. To maximize partial credit, be sure to draw out the products of each reaction you propose. You do not need to draw mechanisms for full credit. (7 points) o by OR ОMe