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- Using the mechanism for the acid-catalyzed hydrolysis of an ester as your guide, write the mechanism— showing all the curved arrows—for the acid-catalyzed reaction of acetic acid and methanol to form methyl acetate. Use HB+ and :B to represent the proton-donating and proton-removing species, respectively.Using the reaction shown in Box (the attack of an amine on the carbonyl group of a ketone) as a starting point, draw curved arrows to represent the base-catalyzed reaction (when the group —B: is present).Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the major product of this acid-base reaction. Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore inorganic byproducts.
- please,complete the following reactions.Given the information pictured, The final step of the reaction sequence uses PhLi. Provide a reason and possible mechanism by which this final elimination and hydrolysis reaction would occur.Draw arrow pushing mechanism, complete the structure in step 4 and select the option that describes the final structure (acetal, hemiacetal, or hydrate)
- Complete the mechanism for the hydrolysis below by adding any missing bonds, charges, nonbonding electrons, and curved arrows.Why are the carboxylic acid groups added in a syn orientation during hydrolysis for the following reaction?Please provide a picture of the drawn out arrow pushing mechanism for the pictured reaction...