Two Step Syntheses. You may use any inorganic reagent. You may use any organic reagent of...
Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organic reagent of TWO carbons or less: 4. Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organi c reagent of TWO carbons or le a) NO2 b) CO2H c) OH d) e) NO2 NO2 Br CI CI CO2H Br
IV. Synthesis Review Complete the following syntheses, using any organic or inorganic reagent necessary. Show all reactions conditions, and intermediate products ?? Br ?? CH CH3 CH2CH2OH
2. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each step and the product of each step. Special conditions: You must use cyclopentadiene as your starting material for all syntheses. You may use organic reagents containing 4 or fewer carbons, and any inorganic reagents. For any Diels-Alder reaction that you use (necessary for all targets!), the dienophile must be an a,ß-unsaturated carbonyl compound. Target 1: HO D Target 2: Doe Target 3: ro Target...
One-step synthesis: Design a synthesis, showing all of the reagents and products along the way. You may use any inorganic reagent and any organic reagent of two carbons or less. 3) НО. НО ? + En
4. (8 points) Devise multi-step syntheses for the following two targets. You must use the given starting materials as the only carbon source. You can use any other organic and inorganic reagents. steps a. V OH - starting material target
Propose multi-step chemical syntheses for the product on the right from the starting material provided, they require more than one step. You can use any reagent with up to four carbons. Show the product for each step in your synthesis. 5. 110 points] Chose TWO of the following transformations and propose multi-step chemical syntheses for the product on the right from the starting material provided. All syntheses require more than one step. You can use any reagent with up to...
For 1 - 3, design reasonable syntheses of each of the target molecules using the provided starting material and organic and inorganic reagents of your choice. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Please put all your answers on this sheet. Write your answers like this (actual number of starting steps may vary)material reagent(s) reagent(s) ABCD target Two equally reasonable routes are possible Can you find them both? (For...
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...
Page 4 Propose reasonable syntheses for the following compo compounds and using any other necessary organic intermediates formed to receive full credit. Assume separated. ng compounds beginning with the indicated organic or inorganic reagents. Show all sume any isomers formed can easily be [3% +6% marks] c. Provide any required reagents and give the stru following synthetic scheme. If more than one reaga steps. ve the structures of the intermediates in the one reagent is required, please number the Bra,...
Devise a synthesis of the following compound from styrene (CH3CH=CH). You may use any inorganic or organic reagents. More than one step is required. CH3CH2COOH Part 1 out of 2 CHECH=CH2 12] H202, OH