14. (6 points) Identify what reagents you would use to synthesize the following compound with a...
14. (6 points) Identify what reagents you would use to synthesize the following compound with a Robinson annulation reaction: 15. (6 points) Propose a reasonable step-by-step mechanism for the following conversion: Get morgon 3.1
(6 points) Identify what reagents you would use to synthesize the following compound with a Robinson annulation reaction: (6 points) Propose a reasonable step-by-step mechanism for the following conversion: NaOH jd met H2O
can you answer all the questions? thanks 14. (6 points) Identify what reagents you would use to synthesize the following compound with a Robinson annulation reaction: 15. (6 points) Propose a reasonable step-by-step mechanism for the following conversion: Še ena on . NaOH HO
Show the two (neutral) organic starting materials that would be used to synthesize the following compound via a Robinson Annulation reaction.
Question 4 (14 points) Propose a synthesis. You may use any reagents you wish. H2 Question 5. (15 points). Perform a Robinson Annulation on the following reagents, showing full formal arrow-pushing. Be sure to end as a ketone! Clearly indicate your product in your answer. You may use any reagents you wish. NH2 Question 6. (20 points) Draw the following reagent in its most stable chair form. Show your process to ensure partial credit. CHO HO OH HO OH CH,OH
6) Predict missing starting compound and reagent in the following transformations (14 points). a. Robinson annulation reaction: Michael addition followed by aldol condensation O- NaOEt EtOH aldol condensation product Michael addition product aldol addition product
6. (12 points) Synthesize the following compound from acetophenone. Use may use any available organic and inorganic reagents: from
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
what does it mean to synthesize something ? 12. : Synthesize the following compound from toluene and any other needed reagents. (6 points)
How would you synthesize the following compound from acetylene and reagents in the table? Choose the most efficient route. Specify reagents using letters from the table, first reagent on the left. Example: ab H H CH3CH2CH2 CH2CH3 a. Br2 b. CH3CH I Reagents available d. CH3 CH2CH2CH2Br g. KOH/ ethanol e. Hy / Lindlar's catalyst | h. NaNH / NH3 f. 1. BHz in THF 2. H2O2 in NaOH c. CH3 CH, CH,Br Reagents (in order of use) are Submit...