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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![22. a. Label the reactive features of the following reactants, select the most reactive feature, then
write and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion will
start to develop, and/or if aromatic character will be lost as a result of a reaction between these
molecules.
d-caprolactone with 2 equivalents of ethylamine
b. Use mechanism arrows to illustrate the reaction that occurs.
If applicable, use stabilization resources to deal with the carbocation, carbon radical, or
carbanion that starts to develop during the reaction, and draw the structure of any resonance-
stabilized intermediate.
Continue labelling and diagramming the reaction until you find the major stable
product(s).
Finally, state the stereochemistry of the major product(s) and use either Fisher projection
or perspective formula representations to illustrate that stereochemistry.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F1f347d8e-0515-4122-ae92-3978bb297a13%2Fde7d0ee5-5518-4d8c-8a2c-6dc4a1dc8e8f%2Fwwyp4v_processed.jpeg&w=3840&q=75)
Transcribed Image Text:22. a. Label the reactive features of the following reactants, select the most reactive feature, then
write and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion will
start to develop, and/or if aromatic character will be lost as a result of a reaction between these
molecules.
d-caprolactone with 2 equivalents of ethylamine
b. Use mechanism arrows to illustrate the reaction that occurs.
If applicable, use stabilization resources to deal with the carbocation, carbon radical, or
carbanion that starts to develop during the reaction, and draw the structure of any resonance-
stabilized intermediate.
Continue labelling and diagramming the reaction until you find the major stable
product(s).
Finally, state the stereochemistry of the major product(s) and use either Fisher projection
or perspective formula representations to illustrate that stereochemistry.
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