Which of the following best describes the hydrolysis of thioesters?
The hydrolysis of thioesters involves a nucleophilic acyl substitution mechanism, producing a carboxylic acid and a thiol.
Which of the following refers to the process of hydrolysis in the context of thioesters?
Hydrolysis of thioesters refers to the reaction where a thioester is converted into a carboxylic acid and a thiol, following a nucleophilic acyl substitution mechanism.
What are the products of acid-catalyzed hydrolysis of thioesters?
The products of acid-catalyzed hydrolysis of thioesters are a carboxylic acid and a thiol.
What is the first step in the nucleophilic acyl substitution mechanism for thioester hydrolysis?
The first step in the nucleophilic acyl substitution mechanism for thioester hydrolysis is protonation.
What is saponification in the context of thioester hydrolysis?
Saponification in the context of thioester hydrolysis refers to the basic hydrolysis process that produces a carboxylate anion and a thiol.
What happens to the carboxylic acid in basic hydrolysis of thioesters?
In basic hydrolysis of thioesters, the carboxylic acid is deprotonated to form a carboxylate anion.
What is the role of proton transfer in the hydrolysis of thioesters?
Proton transfer is involved in steps 1, 3, and 5 of the nucleophilic acyl substitution mechanism during thioester hydrolysis.
What is the leaving group in the hydrolysis of thioesters?
The leaving group in the hydrolysis of thioesters is typically a thiol.
What is the final step in the acid-catalyzed hydrolysis of thioesters?
The final step in the acid-catalyzed hydrolysis of thioesters is deprotonation.
What is the main difference between acid-catalyzed and basic hydrolysis of thioesters?
The main difference is that acid-catalyzed hydrolysis produces a carboxylic acid, while basic hydrolysis (saponification) results in a carboxylate anion.