Provide multistep synthesis for the following target molecule from
the indicated starting materials
Provide multistep synthesis for the following target molecule from the indicated starting materials NH2 from 0...
Provide a reasonable multistep synthesis of the following molecule from the indicated starting material, using any reagents necessary. (Please include the product and reagents of each individual step in your synthesis. DER
(4) Propose a synthesis of the target molecule from the indicated starting materials. Cau- tion! Long, inefficient syntheses are penalized. لل H NH2 (a) [12 points] CH (b) [12 points] 2 Ph Ph Ph CH acetophenone All of the carbons in the target must come from acetophenone.
Provide a multi-step synthesis for the following target molecule from the indicated starting material. T- from OH and он
Provide a multistep synthesis for the desired product using the indicated starting materials. You may use any additional organic or inorganic reagents. Do not draw any curved-arrow mechanisms. The best answ will require nine or fewer steps. OH 었 OET NH2 Starting Materials NH3 OH Desired Product
9) (marks = 3) Provide a reasonable multistep synthesis of the following molecule from the indicated starting material, using any reagents necessary. Please include both a retrosynthesis and a forward synthesis (that includes the product and reagents of each individual step in your synthesis). Meo. = Me Me as a racemic mixture These reagents are your only sources of carbon and both are to be used at different steps of your synthesis
Provide a multistep synthesis for the product using the indicated start materials. You may use any additional reagents. use less than 9 steps OH OEt NH2 Starting Materials NH3 OH or Desired Product
(4) Propose a synthesis of the target molecule from the indicated starting materials. Cau- tion! Long, inefficient syntheses are penalized. & NH (a) [12 points) (b) [12 points) 2 Ph Ph Ph сн. acetophenone All of the carbons in the target must come from acetophenone.
2. Devise a multistep synthesis of the target molecule from the starting material shown. Show the reagents needed for each step and the product of each step. Do not show any mechanisms.
Bonus: Provide a synthesis for the target molecule starting from Benzene (5 pts). Bonus: Provide a synthesis for the target molecule starting from Benzene (5 pts).
Design a multi-step synthesis for each of the following target molecules from the indicated starting material. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Draw the structures of the diene and the dienophile that reacted to form the Diels-Alder product shown. Provide the missing reagents in this multistep synthesis.