1.) Propose a synthesis for the following general reactions. You may use any other organic or...
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
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
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
9. Propose an efficient synthesis of each molecule below starting from benzene and any other reagents needed (organic or inorganic) A. CI B. CI NO2 Br
Please explain the mechanisms!
1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Multiple steps are required. The number of steps you use does not matter. Reactions should give the desired product as a major product. For full credit show the product of each step (reaction). If you make use of organometallic reagents such as Grignard, Wittig, organolithium, organosodium, organocopper, etc. you must...
Synthesis 1. The following transformations cannot be performed in one step. Provide a sequence of reactions to convert the starting material to the product Show all the reagents and synthetic intermediates You can use any additional carbon sources if needed, but you must use the starting material given We were unable to transcribe this image
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...
8. Alcohols are readily available synthetic starting materials. Propose a series of reactions to achieve the following syntheses starting from alcohols. Clearly show the reagents used for each step and the synthetic intermediates. a. For this synthesis, use the given starting alcohols and any inorganic reagents needed. You may use the two alcohols in separate reactions as needed. M OH + OH ... i
Propose a simple synthesis for the compound shown below, using
the provided starting material and any organic or inorganic
Reagent. Draw all intermediates. (Use alkene and alkyne
reactions)
Use SN1/SN2 or E1/E2 reactions along with addition
reaction to complete the synthesis.
We were unable to transcribe this imageSynthesis 1. The following transformations cannot be performed in one step. Provide a sequence of reactions to convert the "starting material to the "product." Show all the reagents and synthetic intermediates You can use any additional carbon sources if needed, but you must use the starting material given.