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- Q6 Complete the retrosynthetic analysis. Supply all reagents and precursors, for both parts: A and B. Fewest possible reaction paths should be choiun. Part A V Part B Mi2. Provide synthetic route for the following transformation mia CIProvide an arrow pushing mechanism for the following reaction. Include protons and each step clearly indicated. 1. LIAID4 „CH3 H3C 2. H30* fill in products
- Provide a retrosynthetic analysis and forward synthesis for the compound shown below. H- and any other reagent of one carbon or less.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 solution2. Propose a reasonable synthesis of compound 2 from compound 1. Use no more than 4 steps. Он он он 2
- 1. Draw the retrosynthetic analysis of compound A by providing the appropriate disconnection and functional group interconversion with 4-hydroxybenzoic acid as the starting material. Suggest a complete synthetic pathway with the reagents and reaction conditions to synthesise A. он NR2 HO A3. Propose a synthesis from benzene and show each intermediate Br NH₂1. Name these compounds: a) b) H₂C HOCCHCH₂OH ÓC6H5 KOČCHCH₂OH bCGHS b) 2. Show the reagent(s) necessary to carry out this reaction. (CH3)3CCH₂COH H₂C C6H5COCH3 CH3 d) 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCI₂. a) (CH3)3CCH₂COH (CH3);CCH₂&N (CH₂)2 (CH₂);CCH, COCH₂CH(CH₂)2 4. Number these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. C.H.ECI 요 C6H5OCCHCH₂OH OCGH₁ C6H5CNHC(CH3)3 3NHCCHCH₂OH OC6H5 C6H;C=N