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Q: Н
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- Show the retrosynthetic analysis and forward synthesis of the following compounds. 1. د c 2. OCH3Provide a retrosynthetic pathway from the following compound. Indicate reagents needed for each transformation...5. Provide an efficient synthesis for the following transformation. Synthesis with the fewest steps, best yields and best selectivity will get maximum marks. Me,SiQ
- provide a suitable synthesis for the following transformationProvide an arrow pushing mechanism for the following reaction. Include protons and each step clearly indicated. 1. LIAID4 „CH3 H3C 2. H30* fill in productsDevise 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
- 2. Provide synthetic route for the following transformation mia CIProvide all needed reagents and conditions for each step.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 A
- 15. Provide a retrosynthesis for the target molecules shown.List the appropriate reagents that can be used in places with question marks in the following series of reactions.Which reagents should be used to complete the following synthesis. Note it may be more than one step. 1) HNO3/H₂SO4 2) C1₂/FeCl3 1) Cl2/FeCl3 2) HNO3/H2SO4 NaNO3/HC1 1) HC1 2) HNO3 NO₂ CI