4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place t...
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 но ме -O Me
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
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. HH iPr Meo, co Me co, 8. 2. 3. 7. 5. Me NH2 Me MeOCCO Me 6.
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
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 HO Me го ме
Using retrosynthetic analysis,
provide a synthesis for the following molecule. Place the required
reagents next to the arrows and the necessary
HH iPr: + MeOCCO Me 1. 8. 2. 9. 3. 7. 4. 5. Me NH2 6. Me MeOCCO Me
provide a synthesis for the following molecule. Place the required the necessary intermediates in the boxes provided. 4. (12 pts) Using retrosynthetic analysis, a reagents next to the arrows and necessary Me t-Bu MgBr
provide a synthesis for the following molecule. Place the required the necessary intermediates in the boxes provided. 4. (12 pts) Using retrosynthetic analysis, a reagents next to the arrows and necessary Me t-Bu MgBr
Propose a synthesis using the target molecule with
retrosynthetic analysis.
Provide complete reagents for each step of your proposed
synthesis.
from Target molecule
from Target molecule
6. (12 pts) For each the molecules below, provide a retrosynthetic analysis and then give a step-by- step synthetic plan. All the carbon atoms in the final products must come from molecules in the box at the bottom. You may use any other reagents you want to accomplish your synthesis. H3CH2CO Acceptable Carbon Sources: " i hool.com ormar BCH,NH iicuch " OCH CH3
Provide retrosynthetic analysis and synthesize the following
molecule from acetylene and an alkyl halide.
3. Provide retrosynthetic analysis and synthesize the following molecule from acetylene and an alkyl halide: OH