Could the structures below undergo a Fischer esterification reaction? Reaction scheme of benzoic acid and thionyl chloride to fo
rm an unknown product. No, the structures above cannot undergo a Fischer esterification reaction to form an ester. Yes, if the carboxylic acid is heated in the SOCl2 reagent and a small amount of H2SO4 is used as a catalyst.
1 answer:
Answer:
The correct answer is the first option. No, the structures above cannot undergo a Fischer esterification reaction to form an ester.
Explanation:
The reaction that will take place can be found in the attached file. The reaction does not require any catalyst and it cannot undergo a Fischer esterification reaction to form an ester.
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Answer:
Explanation:
Hello there!
In this case, when considering weak acids which have an associated percent dissociation, we first need to set up the ionization reaction and the equilibrium expression:
Now, by introducing x as the reaction extent which also represents the concentration of both H+ and A-, we have:
Thus, it is possible to find x given the pH as shown below:
So that we can calculate the initial concentration of the acid:
Therefore, the percent dissociation turns out to be:
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