Question 4 (14 points) Propose a synthesis. You may use any reagents you wish. H2 Question...
1.) Propose a synthesis for the following general reactions. You may use any other organic or inorganic reagents needed. For each step, show the reagents used and the intermediate formed (Note: I do not need to see any arrow-pushing, only starting materials, reagents, intermediates, and the final product) a.) For each aromatic ring, you must start with a plain benzene. он он CI он
1.) Propose a synthesis for the following general reactions. You may use any other organic or inorganic reagents needed. For each step, show the reagents used and the intermediate formed. (Note: I do not need to see any arrow-pushing, only starting materials, reagents, intermediates, and the final product) a.) For each aromatic ring, you must start with a plain benzene. он он We were unable to transcribe this image
10% Multi Step Reactions 6) Show how you would accomplish the following synthesis in good yields. You may use any reagents that you wish. Hint: Protect 2 different functional groups if you choose to use a Grignard's reagent. :OH : OH но 10% Multi Step Reactions 6) Show how you would accomplish the following synthesis in good yields. You may use any reagents that you wish. Hint: Protect 2 different functional groups if you choose to use a Grignard's reagent....
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
Please answer all components. Question 7 (15 points) Propose a stepwise synthesis for the following reaction. You may use any reagents and/or additional molecules that you wish Question 8 (15 points). Provide a stepwise synthesis for the following reaction. (There are multiple synthesis pathways)
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
Need help with all 4 of these synthesis reactions. Br in first question and wants to see all arrow pushing, intermediates and products. Last three just want the numbered reagents and the intermediate products after each step. No arrow pushing. Homework #1 Name: 1. Explain with a mechanism the observation of the given products. (Hint: You will need the full reaction mechonism including all intermediates and reogents, Show the proper use of electron pushing arrows.) HBr 2. Propose an efficient...
4. Propose a synthesis of 4-Oxohexanal starting with 2-Ethylcyclobutanone. You can use any other reagents you want. (2 points)
4. Synthesis. You may use benzene (that is the starting material for a), any organic reagents that contribute four or fewer carbon atoms to the final product, and any inorganic reagents OH OH HN NH 4. Synthesis. You may use benzene (that is the starting material for a), any organic reagents that contribute four or fewer carbon atoms to the final product, and any inorganic reagents OH OH HN NH
2) Propose a synthesis for the transformation below. You may use any reagent discussed in the course notes or textbook, as well as any additional compound with 2 or fewer C atoms in your solution. (5 marks)