(SYN) How would you synthesize the compound shown here using phenylethanal as your only source of carbon atoms? You may ignore stereochemistry.
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- please help with this question. thank you. Propose an efficient synthesis of for each of the following transformation.(SYN) Show how to carry out the following conversion.Hint: Consider using a protecting group.(SYN) Show how you would synthesize each of these compounds, using butan-1-ol and benzene as your only sources of carbon.
- Supply the structures of compounds A–I in the following synthesis scheme.Kindly help me here. I have excluded some steps in my mechanism as I believe they are unnecessary. Help me decipher the major product and minor product and why.Mechanism, in the space provided below please give the detailed mechanism for the following transformation
- Inactivate the following molecule in TWO steps using any reasonable route. Draw structureI’m having hard time predicting this product of reactions can you please help?I don’t get to synthesize this from an ALCOHOL of two carbons or less and benzene. Chloro, in our notes is a ortho/para directing. So I don’t know how you would get a meta substituted benzene