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3. a,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. :Nu-H Nu H 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. а. b. C. a direct addition d. a 1,2-addition.

3. a,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. :Nu-H Nu H 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. а. b. C. a direct addition d. a 1,2-addition.

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
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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3. a,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. || + :Nu-H Nu H 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. а. b. С. a direct addition d. a 1,2-addition.
Transcribed Image Text:3. a,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. || + :Nu-H Nu H 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. а. b. С. a direct addition d. a 1,2-addition.
6. Show how each of the following transformations might be best accomplished. More than one step may be required. Show all reagents and all intermediate structures. CH3 CH3 CH;CH2-Č-Br CH;CH2-C- NH2 CH3 CH3 a. b. N. OH H only source of carbon C. OH NH2 d. CH3 CH3 CN е. C1 C1
Transcribed Image Text:6. Show how each of the following transformations might be best accomplished. More than one step may be required. Show all reagents and all intermediate structures. CH3 CH3 CH;CH2-Č-Br CH;CH2-C- NH2 CH3 CH3 a. b. N. OH H only source of carbon C. OH NH2 d. CH3 CH3 CN е. C1 C1
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