5. Provide a synthetic approach for the following reactions. Make sure to do the retrosynthetic analysis and then provide the forward reaction sequence. OH Но OH HO HO.
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- 1. Show all steps in the synthesis of 4-methylaniline from toluene. Clearly show all reagents, reactants and products for each step. Toluene -------> --------> 4-methylanilineProvide a reagent that will complete the transformations.2. Propose a synthetic strategy for the following reactions. Make sure to include the structures of all intermediate products. Ph ÇOCH,
- 3. Provide a complete arrow pushing mechanism for the following transformation. H b HO NaOH heatPlease rovide a synthetic approach for the following reactions. Make sure to do the retrosynthetic analysis and then provide the forward reaction sequence.Provide a synthetic approach for the following reactions. Make sure to do the retrosynthetic analysis and then provide the forward reaction sequence. HO OH حمام HO OH محمده HO
- 2. Provide the reagents required to complete the following multi-step synthesis. Write the structure of the product after each synthetic step.4. Provide a synthetic route to the following molecule using benzene and cyclohexane. Reagents cannot contain more than one carbon. Provide a mechanism for the last step of your synthetic route.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
- Supply the reagents that would be needed to perform the following reactions.Perform the syntheses given below using appropriate reagents and necessary mechanisms.Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.