3) Draw a complete, step-wise curved arrow mechanism for the transformation shown below. You may use H-B for any Broensted acid and B- for any Broensted base. (6 points) AlCl3, CICH 3 2) a) Draw the product if Molecule A underwent a [3,3]-sigmatropic rearrangement. Hint, you may want to start by redrawing the starting materials in their reactive conformations. (4 points) Molecule A CH3 CH2 b) Show the complete, step-wise curved arrow mechanism for the above reaction. You may use H-B for any Broensted acid and B- for any Broensted base. You can maximize your chances of partial credit by providing a consistent numbering scheme for your carbons. (9 points)
3) Draw a complete, step-wise curved arrow mechanism for the transformation shown below. You may use H-B for any Broensted acid and B- for any Broensted base. (6 points) AlCl3, CICH 3 2) a) Draw the product if Molecule A underwent a [3,3]-sigmatropic rearrangement. Hint, you may want to start by redrawing the starting materials in their reactive conformations. (4 points) Molecule A CH3 CH2 b) Show the complete, step-wise curved arrow mechanism for the above reaction. You may use H-B for any Broensted acid and B- for any Broensted base. You can maximize your chances of partial credit by providing a consistent numbering scheme for your carbons. (9 points)
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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Transcribed Image Text:3) Draw a complete, step-wise curved arrow mechanism for the transformation shown below.
You may use H-B for any Broensted acid and B- for any Broensted base. (6 points)
AlCl3, CICH 3
![2) a) Draw the product if Molecule A underwent a [3,3]-sigmatropic rearrangement. Hint, you
may want to start by redrawing the starting materials in their reactive conformations. (4
points)
Molecule A
CH3
CH2
b) Show the complete, step-wise curved arrow mechanism for the above reaction.
You may use H-B for any Broensted acid and B- for any Broensted base. You can
maximize your chances of partial credit by providing a consistent numbering
scheme for your carbons. (9 points)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fe11d7b0a-4708-45af-84ee-396bdfbd9279%2F5fdda273-9c21-4b1d-b196-6a9bfac2ba09%2Fabigknt_processed.jpeg&w=3840&q=75)
Transcribed Image Text:2) a) Draw the product if Molecule A underwent a [3,3]-sigmatropic rearrangement. Hint, you
may want to start by redrawing the starting materials in their reactive conformations. (4
points)
Molecule A
CH3
CH2
b) Show the complete, step-wise curved arrow mechanism for the above reaction.
You may use H-B for any Broensted acid and B- for any Broensted base. You can
maximize your chances of partial credit by providing a consistent numbering
scheme for your carbons. (9 points)
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