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a. Write the complete stepwise mechanism for the reaction above. Show all intermediate structures and all electron flow with arrows. b. Refer to Exhibit 23-2. This reaction is an example of: a. an intramolecular Claisen condensation b. an intramolecular aldol condensation C. a Robinson annulation d. a Michael reaction c. The product of this reaction is: a. a 6, y-unsaturated aldehyde b. an a, 6-unsaturated ketone an a, 6-unsaturated aldehyde d. an enol C. 3.

a. Write the complete stepwise mechanism for the reaction above. Show all intermediate structures and all electron flow with arrows. b. Refer to Exhibit 23-2. This reaction is an example of: a. an intramolecular Claisen condensation b. an intramolecular aldol condensation C. a Robinson annulation d. a Michael reaction c. The product of this reaction is: a. a 6, y-unsaturated aldehyde b. an a, 6-unsaturated ketone an a, 6-unsaturated aldehyde d. an enol C. 3.

Chemistry
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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2. Consider the reaction below to answer the following question(s): H. + Но NaOEt H. ELOH a. Write the complete stepwise mechanism for the reaction above. Show all intermediate structures and all electron flow with arrows. b. Refer to Exhibit 23-2. This reaction is an example of: а. an intramolecular Claisen condensation b. an intramolecular aldol condensation с. a Robinson annulation d. a Michael reaction c. The product of this reaction is: a 6, y-unsaturated aldehyde an a, 6-unsaturated ketone an a, 6-unsaturated aldehyde а. b. C. d. an enol 3. a,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. :Nu-H Nu a. Draw a resonance form for the unsaturated carbonyl that accounts for this reactivity. b. This reaction is called reaction. a 1,2-conjugate addition. an electrophilic addition. a direct addition a. b. с. d. a 1,2-addition.
Transcribed Image Text:2. Consider the reaction below to answer the following question(s): H. + Но NaOEt H. ELOH a. Write the complete stepwise mechanism for the reaction above. Show all intermediate structures and all electron flow with arrows. b. Refer to Exhibit 23-2. This reaction is an example of: а. an intramolecular Claisen condensation b. an intramolecular aldol condensation с. a Robinson annulation d. a Michael reaction c. The product of this reaction is: a 6, y-unsaturated aldehyde an a, 6-unsaturated ketone an a, 6-unsaturated aldehyde а. b. C. d. an enol 3. a,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. :Nu-H Nu a. Draw a resonance form for the unsaturated carbonyl that accounts for this reactivity. b. This reaction is called reaction. a 1,2-conjugate addition. an electrophilic addition. a direct addition a. b. с. d. a 1,2-addition.
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