Ph y Ome 3. Synthesize the following acetal Me Retrosynthetic Analysis | Synthesis
1. Synthesize the following ester Retrosynthetic Analysis Synthesis
4.Synthesize the following sulfide ci Retrosynthetic Analysis Synthesis
2. Synthesize the following amide ci' Retrosynthetic Analysis Synthesis
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
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....
Use retrosynthetic analysis to suggest a way to synthesize 2,3-dimethyl-3-pentanol using the Grignard reaction. (Click and drag the appropriate images to the reactant positions in the following reaction.) Use retrosynthetic analysis to suggest a way to synthesize 2,3-dimethyl-3-pentanol using the Grignard reaction. (Click and drag the appropriate images to the reactant positions in the following reaction.)Use retrosynthetic analysis to suggest a way to synthesize 2,3-dimethyl-3-pentanol using the Grignard reaction. (Click and drag the appropriate images to the reactant positions in...
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. Me HO Me го ме
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 Me MeOCCO,Me 1. 8. 2. 9 3 7. 4. 5 NH2 6 MeOCCO Me