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- Propose how you could synthesize the following compound, using a substitution reaction. Propose a nucleophile, a solvent, and an electrophile. Show the curved-arrow mechanism of the reaction. Finally, draw the transition state of the reaction.Propose a detailed mechanism for the reaction below (in the attached picture), showing the structure of thestable intermediate and using curved arrows to indicate electron flow in each stepWhat is the mechanism for the entire reaction below?
- Provide the mechansim using curved arrows of the reaction of p-t-butyl phenol treated with acetic anhydride in AlCl3. Include resonance stabilized intermediates and if more than one product is formed, label them as major, minor, etc. thank you for the helpBelow is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?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.
