Under certain conditions, 1,3-cyclopentadiene can function both as a diene and a dienophile. Draw a structural formula for the Diver reaction of 1,3-cyclopentadiene with itself. . You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. QCP raw a structural formula for the product of this Diels-Alder reaction, including all stereoisomers of the product. COOEt CHO COOEt
Under certain conditions, 1,3-cyclopentadiene can function both as a diene and a dienophile. Draw a structural formula for the Diver reaction of 1,3-cyclopentadiene with itself. . You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. QCP raw a structural formula for the product of this Diels-Alder reaction, including all stereoisomers of the product. COOEt CHO COOEt
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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G.165.
![C
Under certain conditions, 1,3-cyclopentadiene can function both as a diene and a dienophile. Draw a structural formula for the Diels-Alder adduct formed by
reaction of 1,3-cyclopentadiene with itself.
. You do not have to consider stereochemistry.
• You do not have to explicitly draw H atoms.
C P
000 IF
Draw a structural formula for the product of this Diels-Alder reaction, including all stereoisomers of the product.
COOEt
a
CHO
=
. Use the wedge/hash bond tools to indicate stereochemistry where it exists.
COOEt
The narrow end of the hashed or solid wedge bonds must begin at the chiral center.
• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
.
Separate multiple products using the + sign from the drop-down menu.
C P
opy asto
O- [F](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F146ba547-3393-4257-a101-1e7cee66946f%2F7b27cdc6-8b8e-4156-9c30-41c74fd9372c%2Fv3fcv7l_processed.jpeg&w=3840&q=75)
Transcribed Image Text:C
Under certain conditions, 1,3-cyclopentadiene can function both as a diene and a dienophile. Draw a structural formula for the Diels-Alder adduct formed by
reaction of 1,3-cyclopentadiene with itself.
. You do not have to consider stereochemistry.
• You do not have to explicitly draw H atoms.
C P
000 IF
Draw a structural formula for the product of this Diels-Alder reaction, including all stereoisomers of the product.
COOEt
a
CHO
=
. Use the wedge/hash bond tools to indicate stereochemistry where it exists.
COOEt
The narrow end of the hashed or solid wedge bonds must begin at the chiral center.
• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
.
Separate multiple products using the + sign from the drop-down menu.
C P
opy asto
O- [F
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