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A: Molarity of NaOH = 0.15 mol/LMolarity of weak acid = 0.20 mol/LpKa = 4.06
Q: Н
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- 5. Provide an efficient synthesis for the following transformation. Synthesis with the fewest steps, best yields and best selectivity will get maximum marks. Me,SiQShow the retrosynthetic analysis and forward synthesis of the following compounds. 1. د c 2. OCH3Provide a retrosynthetic analysis and forward synthesis for the compound shown below. H- and any other reagent of one carbon or less.
- Provide all needed reagents and conditions for each step.provide a suitable synthesis for the following transformationDevise 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 CI1. 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 A15. Provide a retrosynthesis for the target molecules shown.
- Provide an arrow pushing mechanism for the following reaction. Include protons and each step clearly indicated. 1. LIAID4 „CH3 H3C 2. H30* fill in productsList 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