3) Which of these acids would undergo easy decarboxylation in boiling aqueous acid? Draw the product of those that would decarboxylate. مانه H میل سمون سهره O-H
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- The following molecule undergoes an intramolecular reaction in the presence of pyrrolidinium acetate, the protonated form of pyrrolidine. Draw the product of this reaction, assuming that a dehydration reaction takes place.Which of these amine will react fastest in a reductive amination reaction?Rank the attached compounds in order of increasing acidity.
- Which of the following compounds will decarboxylate (lose carbon dioxide) in the presence ofaqueous acid and heat? Provide the product for one of the compounds that can be decarboxylated.Rank the following esters from most reactive to least reactive toward hydrolysis:Rank the derivatives of phenol in order of increasing acidity (Please explain) 
- Rank the derivatives of benzoic in order of increasing acidity:Rank the following compounds in order of their acidity.Show how acid derivatives hydrolyze to carboxylic acids under either acidic or basicconditions. Explain why some acid derivatives (amides, for example) require muchstronger conditions for hydrolysis than other derivatives.