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14. (6 points) Identify what reagents you would use...
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...
(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
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:
Question 4 (14 points) Propose a synthesis. You may use any reagents you wish. H2 Question...
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
15. (6 points) Propose a reasonable step-by-step mechanism for the following conversion: NaOH & Non 8....
15. (6 points) Propose a reasonable step-by-step mechanism for the following conversion: NaOH & Non 8. i H20
3) Identify the reagents that you would use to produce the following compounds using a Claisen...
3) Identify the reagents that you would use to produce the
following compounds using a Claisen condensation.
4) For the following reaction, predict the major product and
propose a mechanism for its formation.
3. Identify the reagents that you would use to produce the following compounds using a Claisen condensation. 4. For each of the following reactions, predict the major product and propose a mechanism for its formation. 1) LDA. 2) CHal
identify which compound is more acidic and explain your choice. or each of the following compounds,...
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...
6) Predict missing starting compound and reagent in the following transformations (14 points). a. Robinson annulation...
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
8) Choose 2 of the following transformations and list the reagents (they will all take more...
8) Choose 2 of the following transformations and list the reagents (they will all take more than onel) you would use to synthesize that molecule. (8 points). Bonus: the other 2 syntheses are worth 4 bonus points each. 7) For the following elimination reactions, predict the major product. 2 Points each. Label each as E, Z, or NA. (1 Point each) E, Z or NA Br NaOH NaOH Br Br NaOH NaO Bu Be Br 6) For the following reaction,...
Please solve all the problem questions Propose a synthesis for compound with certain the following reagents....
Please solve all the problem questions
Propose a synthesis for compound with certain the following reagents. Grignard reagent Geranial, citral (3,7-dimethylocta- 2,6-dienal ) OH Product / Identify the complete reaction with all reagents and products in addition to the reaction mechanisms ✓ Reference the bibliography used, (scientific Jounal articles) ✓ Describe step by step the synthesis methodology in laboratory.
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
14. (6 points) Identify what reagents you would use to synthesize the following compound with 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
15. (6 points) Propose a reasonable step-by-step mechanism for the following conversion: NaOH & Non 8. i H20
3) Identify the reagents that you would use to produce the
following compounds using a Claisen condensation.
4) For the following reaction, predict the major product and
propose a mechanism for its formation.
3. Identify the reagents that you would use to produce the following compounds using a Claisen condensation. 4. For each of the following reactions, predict the major product and propose a mechanism for its formation. 1) LDA. 2) CHal
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...
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
8) Choose 2 of the following transformations and list the reagents (they will all take more than onel) you would use to synthesize that molecule. (8 points). Bonus: the other 2 syntheses are worth 4 bonus points each. 7) For the following elimination reactions, predict the major product. 2 Points each. Label each as E, Z, or NA. (1 Point each) E, Z or NA Br NaOH NaOH Br Br NaOH NaO Bu Be Br 6) For the following reaction,...
Please solve all the problem questions
Propose a synthesis for compound with certain the following reagents. Grignard reagent Geranial, citral (3,7-dimethylocta- 2,6-dienal ) OH Product / Identify the complete reaction with all reagents and products in addition to the reaction mechanisms ✓ Reference the bibliography used, (scientific Jounal articles) ✓ Describe step by step the synthesis methodology in laboratory.
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