2. Write a reaction for the formation of methyl salicylate, an ester that smells like wintergreen, from salicylic acid and methanol. Circle the ester functional group. 3. Explain why is the reaction in question 2 called a "condensation" reaction. What is the other product of the reaction besides the ester?
2. Write a reaction for the formation of methyl salicylate, an ester that smells like wintergreen, from salicylic acid and methanol. Circle the ester functional group. 3. Explain why is the reaction in question 2 called a "condensation" reaction. What is the other product of the reaction besides the ester?
World of Chemistry, 3rd edition
3rd Edition
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Chapter20: Organic Chemistry
Section: Chapter Questions
Problem 54A
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Question
![2. Write a reaction for the formation of methyl salicylate, an ester that smells like
wintergreen, from salicylic acid and methanol. Circle the ester functional group.
3. Explain why is the reaction in question 2 called a "condensation" reaction. What is the
other product of the reaction besides the ester?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F5504642f-0145-4427-b5f2-66a9310e79bc%2F3392c8fb-21e8-4107-b600-935b5c5b9896%2F16vzgco_processed.jpeg&w=3840&q=75)
Transcribed Image Text:2. Write a reaction for the formation of methyl salicylate, an ester that smells like
wintergreen, from salicylic acid and methanol. Circle the ester functional group.
3. Explain why is the reaction in question 2 called a "condensation" reaction. What is the
other product of the reaction besides the ester?
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