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- 4. Provide a retrosynthetic analysis and forward synthesis for the following molecule. (Construct flow charts (a.k.a. flow diagrams) to show how to separate each of the following pairs ofwater insoluble compounds:a) a carboxylic acid and a neutral compound (e.g., a hydrocarbon, R-H);b) a neutral compound and an amine;c) a phenol, a carboxylic acid and an amine.Devise a synthesis for benzophenone. You may only use benzene and formaldehyde as sources of carbon. You may use any other reagents necessary to carry out the transformations. typed solution
- Give detailed Solution with explanation neededTo synthesize trans-cinnamic acid from benzaldehyde (PhCHO) and acetic anhydride (Ac2O) under basic, refluxing conditions to exemplify the Perkin condensation. 1. Draw the complete chemical reaction to be carried out. 2. Provide a complete arrow-pushing mechanism for the synthesis of trans-cinnamic acid. 3. Briefly describe the role of water, Na2CO3, and HCl in the isolation of the product. Draw the structure of the product at basic pH (after Na2CO3 addition) and at acidic pH (after HCl addition).2. Write out a detailed recipe for the preparation of benzalacetophenone. formalism) for the preparation of ben
