For this problem, we have to draw the major product formed when the compound shown below is heated with CH3OH.
In this case, we have a carboxylic acid reacting with alcohol which will proceed to a
The mechanism Fischer esterification follows this series of steps:
(1) Protonation of carbonyl
(2) Nucleophilic attack of alcohol
(3) Proton transfer of -OH to the -OR group
(4) Reformation of C=O group (elimination)
(5) Deprotonation of the C=O+H group
Draw the major organic product formed when the compound shown below is heated with CH3OH.
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What scientific concept do you need to know in order to solve this problem?
Our tutors have indicated that to solve this problem you will need to apply the Fischer Esterification concept. You can view video lessons to learn Fischer Esterification. Or if you need more Fischer Esterification practice, you can also practice Fischer Esterification practice problems.
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