We need at least 10 more requests to produce the answer.
0 / 10 have requested this problem solution
The more requests, the faster the answer.
2. Perform a retrosynthetic analysis on the following molecule from the given starting materials (13 pts)....
1. Perform a retrosynthetic analysis on the following molecule from the given starting materials (13 pts). Me Me Ph 1. 9 2. 10. 3. 6. 4. 7. 5.
1. Perform a retrosynthetic analysis on the following molecule from the given starting materials (13 pts). Me Me Ph 1. 9. 2 10. 3. 6. 4. 7. 5. 8.
Perform a retrosynthetic analysis on the following molecule from the given starting materials (13 pts). Me Me EN Ph 1. 9. 2 10. 3. 6. 4. 7. 5. 8.
please can you help 2. Perform a retrosynthetic analysis on the following molecule from the given starting materials (13 pts). Me e Me Me Me O.PT 1 11. 2 3. 10 Me Me Me Me Br
Perform a retrosynthetic analysis on the following molecule from the given starting materials. yes, quite difficult Me Me GEN Ph 1. 9. 2. 10. 3. 6. 4. 7. 5. 8.
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5. 6. 3. 2. NH2 O) 08 4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5....
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. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Η. Η Me MeOCCO,Me 1. 8. 2. 9 3 7. 4. 5 NH2 6 MeOCCO Me
(d) Perform a retrosynthetic analysis of molecule A. Using propiophenone as starting material outline the forward synthesis also. Explain how a similar route could be taken to afford a mixture of diastercoisomers B and C OH OH propiophenone
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Η Η N iPr MeO2C CO Me co 1. 8. 2. 9. 3. 7. 4. 5. Me NH2 6. Me MeOCCO Me