o synthesize trans-cinnamic acid from benzaldehyde (PhCHO) and acetic anhydride (Ac2O) under basic, refluxing conditions to exemplify the Perkin condensation. 1. Draw the complete chemical reaction to be carried out. 2. Provide a complete arrow-pushing mechanism for the synthesis of trans-cinnamic acid. 3. Briefly describe the role of water, Na2CO3, and HCl in the isolation of the product. Draw the structure of the product at basic pH (after Na2CO3 addition) and at acidic pH (after HCl addition).
o synthesize trans-cinnamic acid from benzaldehyde (PhCHO) and acetic anhydride (Ac2O) under basic, refluxing conditions to exemplify the Perkin condensation. 1. Draw the complete chemical reaction to be carried out. 2. Provide a complete arrow-pushing mechanism for the synthesis of trans-cinnamic acid. 3. Briefly describe the role of water, Na2CO3, and HCl in the isolation of the product. Draw the structure of the product at basic pH (after Na2CO3 addition) and at acidic pH (after HCl addition).
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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To synthesize trans-cinnamic acid from benzaldehyde (PhCHO) and acetic anhydride
(Ac2O) under basic, refluxing conditions to exemplify the Perkin condensation.
1. Draw the complete
2. Provide a complete arrow-pushing mechanism for the synthesis of trans-cinnamic acid.
3. Briefly describe the role of water, Na2CO3, and HCl in the isolation of the product. Draw the
structure of the product at basic pH (after Na2CO3 addition) and at acidic pH (after HCl
addition).
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