Provide a stepwise synthesis for the following compound using benzyl alcohol as you only source of...
7) Provide a stepwise synthesis for the following compound using benzyl alcohol as your only source of carbon and using any other reagents necessary. OH OH benzyl alcohol
please answer and show work for stepwise synthesis and other questions. 1. Provide a stepwise synthesis for the dipeptide Ser-Phe. Draw all steps including protecting groups. H2N-CH-C-OH H2N-CH-C-OH CH2 Phe Ser 2. Using ethyl 3-methylbutanoate as your only source of carbon and using any other reagents necessary, propose a stepwise synthesis for the following conversion. 3. Provide the reagents necessary to carry out the following conversion. 4. Provide the structures of the products in each step of the following reaction...
Write out a synthesis of benzyl benzoate using benzyl alcohol at the only source of carbon atoms.
Propose a stepwise synthesis for N-propylbutanamide. using 1-proanol and/or carbon dioxide as your only source of carbon and using any other reagents necessary. Detail how the final product could be identified using a spectroscopic method.
using basic reactions and grignard. Outline a synthesis of the following compound from the compounds below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. 2 OH , CH3 CH3 from 2 OH CH CH3 Outline a synthesis of the following compound from the compounds below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. 2 OH , CH3 CH3 from 2 OH CH CH3
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) он Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic...
Outline a synthesis of the following compound from the compound below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. Ignore E/Z stereoisomers for the product alkene. from as the only source of carbon Outline a synthesis of the following compound from the compound below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. Ignore E/Z stereoisomers for the product alkene. from as the only source...
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) other reagents glven) MS, Bones он Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons...
3. Synthesize the following alcohol using ethyne as the only source of carbon atoms. Any other reagents needed may be used. You can use as many molecules of ethyne as necessary H-CEC-H HO ethyne target alcohol 3. Synthesize the following alcohol using ethyne as the only source of carbon atoms. Any other reagents needed may be used. You can use as many molecules of ethyne as necessary H-CEC-H HO ethyne target alcohol
Using only 1-butanol as your source of carbom, provide a synthesis for the following compound. Using only 1-butanol as your source of carbon, provide a synthesis for the following compound. You may use multiple equivalents of 1-butanol (use it more than once in the synthesis) Please use reactions that give the desired product as the major product Do not use the acetoacetic ester or malonic ester synthesis Show the product for each reaction step