2 1 Group activity: Use molecular model to convert the given 3D perspective structure to Newman projection around C-C bond on the template provided. Fill in the substituent for the most stable conformation in the templates provided. H H OH Br OH CH Y/ 3D of most stable conformation ΕΙ Fischer projection of most stable conformation most stable conformation Use the molecular model of chair conformation of cyclohexane and fill in the substituents in the template provided for chair conformation and complete the Newman projections showing only substituents for given molecules. Circle the chair conformation which is more stable. 1) cis-3-isopropylcyclohexanol 2) trans-3-Isopropylcyclohexaol QO
2 1 Group activity: Use molecular model to convert the given 3D perspective structure to Newman projection around C-C bond on the template provided. Fill in the substituent for the most stable conformation in the templates provided. H H OH Br OH CH Y/ 3D of most stable conformation ΕΙ Fischer projection of most stable conformation most stable conformation Use the molecular model of chair conformation of cyclohexane and fill in the substituents in the template provided for chair conformation and complete the Newman projections showing only substituents for given molecules. Circle the chair conformation which is more stable. 1) cis-3-isopropylcyclohexanol 2) trans-3-Isopropylcyclohexaol QO
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...
Related questions
Question
![2
1
Group activity:
Use molecular model to convert the given 3D perspective structure to Newman projection
around C-C bond on the template provided. Fill in the substituent for the most stable
conformation in the templates provided.
H
H
OH
Br
OH
CH
Y/
3D of most stable
conformation
ΕΙ
Fischer projection
of most stable
conformation
most stable
conformation
Use the molecular model of chair conformation of cyclohexane and fill in the substituents in the
template provided for chair conformation and complete the Newman projections showing only
substituents for given molecules. Circle the chair conformation which is more stable.
1) cis-3-isopropylcyclohexanol
2) trans-3-Isopropylcyclohexaol
QO](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F76caad89-0a9c-4ee9-9646-c51903c3da74%2Fb5d2be28-4f3d-4046-85a8-22b060736fa8%2Fo0zgfg_processed.jpeg&w=3840&q=75)
Transcribed Image Text:2
1
Group activity:
Use molecular model to convert the given 3D perspective structure to Newman projection
around C-C bond on the template provided. Fill in the substituent for the most stable
conformation in the templates provided.
H
H
OH
Br
OH
CH
Y/
3D of most stable
conformation
ΕΙ
Fischer projection
of most stable
conformation
most stable
conformation
Use the molecular model of chair conformation of cyclohexane and fill in the substituents in the
template provided for chair conformation and complete the Newman projections showing only
substituents for given molecules. Circle the chair conformation which is more stable.
1) cis-3-isopropylcyclohexanol
2) trans-3-Isopropylcyclohexaol
QO
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