Draw the conformation that results. Start by adding a cyclohexane template, and then edit H groups to create the second ring. 1. Choose a chair from the Templates toolbar at the bottom. Make sure it's the appropriate chair, including any heteroatoms. 2. Replace the appropriate hydrogens with the appropriate -CH, or other groups. Important: Never delete the hydrogen atoms or bonds in the ring or directly attached to the ring. Also, do not try to move them by drag and drop. them! If you are told your answer is incorrect, use the Undo button to go back, or start over by deleting the structure and re-adding the chair from the te interpreted. CH3 H. H [6] 15] N [5) [1]
Draw the conformation that results. Start by adding a cyclohexane template, and then edit H groups to create the second ring. 1. Choose a chair from the Templates toolbar at the bottom. Make sure it's the appropriate chair, including any heteroatoms. 2. Replace the appropriate hydrogens with the appropriate -CH, or other groups. Important: Never delete the hydrogen atoms or bonds in the ring or directly attached to the ring. Also, do not try to move them by drag and drop. them! If you are told your answer is incorrect, use the Undo button to go back, or start over by deleting the structure and re-adding the chair from the te interpreted. CH3 H. H [6] 15] N [5) [1]
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
I don't know where to place the 10 carbons. And need help with the other question.
![Part A
Draw the conformation that results.
Start by adding a cyclohexane template, and then edit H groups to create the second ring.
1. Choose a chair from the Templates toolbar at the bottom. Make sure it's the appropriate chair, including any heteroatoms.
2. Replace the appropriate hydrogens with the appropriate -CH3 or other groups.
Important: Never delete the hydrogen atoms or bonds in the ring or directly attached to the ring. Also, do not try to move them by drag and drop. These actions wi
them!
If you are told your answer is incorrect, use the Undo button to go back, or start over by deleting the structure and re-adding the chair from the templates. You will
interpreted.
CH3
H
15]
[6]
N
[5]
[1]
CI
[4]
Br
[2]
< 1 of 1 >
F
H.
H.
cis-decalin
- bridgehead
carbons
Submit
Previous Answers Request Answer
X Incorrect; Try Again; 2 attempts remaining
Your answer should have 10 carbon atoms.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F7aa4f678-69cb-4a7f-b4f7-c81e0a793bd9%2F57a60e9a-5d23-4dd5-bd22-8685b2d04ef3%2F6807x8b_processed.png&w=3840&q=75)
Transcribed Image Text:Part A
Draw the conformation that results.
Start by adding a cyclohexane template, and then edit H groups to create the second ring.
1. Choose a chair from the Templates toolbar at the bottom. Make sure it's the appropriate chair, including any heteroatoms.
2. Replace the appropriate hydrogens with the appropriate -CH3 or other groups.
Important: Never delete the hydrogen atoms or bonds in the ring or directly attached to the ring. Also, do not try to move them by drag and drop. These actions wi
them!
If you are told your answer is incorrect, use the Undo button to go back, or start over by deleting the structure and re-adding the chair from the templates. You will
interpreted.
CH3
H
15]
[6]
N
[5]
[1]
CI
[4]
Br
[2]
< 1 of 1 >
F
H.
H.
cis-decalin
- bridgehead
carbons
Submit
Previous Answers Request Answer
X Incorrect; Try Again; 2 attempts remaining
Your answer should have 10 carbon atoms.
![Part A
Draw trans-1-ethyl-2-methylcyclohexane in its lowest energy conformation.
1. Choose a chair from the Templates toolbar at the bottom. Make sure it's the appropriate chair, including any heteroatoms.
2. Replace the appropriate hydrogens with the appropriate -CH3 or other groups.
Important: Never delete the hydrogen atoms or bonds in the ring or directly attached to the ring. Also, do not try to move them by drag and drop. These actions will break the chair conformation structures. Just replace them!
If you are told your answer is incorrect, use the Undo button to go back, or start over by deleting the structure and re-adding the chair from the templates. You will not lose credit for responses that cannot be interpreted.
2C Q O ® H:
H
CI
Br
Marvin JS
by ChemAxon
Submit
Request Answer
Provide Feedback](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F7aa4f678-69cb-4a7f-b4f7-c81e0a793bd9%2F57a60e9a-5d23-4dd5-bd22-8685b2d04ef3%2Fp32p5ib_processed.png&w=3840&q=75)
Transcribed Image Text:Part A
Draw trans-1-ethyl-2-methylcyclohexane in its lowest energy conformation.
1. Choose a chair from the Templates toolbar at the bottom. Make sure it's the appropriate chair, including any heteroatoms.
2. Replace the appropriate hydrogens with the appropriate -CH3 or other groups.
Important: Never delete the hydrogen atoms or bonds in the ring or directly attached to the ring. Also, do not try to move them by drag and drop. These actions will break the chair conformation structures. Just replace them!
If you are told your answer is incorrect, use the Undo button to go back, or start over by deleting the structure and re-adding the chair from the templates. You will not lose credit for responses that cannot be interpreted.
2C Q O ® H:
H
CI
Br
Marvin JS
by ChemAxon
Submit
Request Answer
Provide Feedback
Expert Solution
![](/static/compass_v2/shared-icons/check-mark.png)
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
This is a popular solution!
Trending now
This is a popular solution!
Step by step
Solved in 3 steps with 2 images
![Blurred answer](/static/compass_v2/solution-images/blurred-answer.jpg)
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Recommended textbooks for you
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
![Organic Chemistry](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
![Chemistry: Principles and Reactions](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
![Elementary Principles of Chemical Processes, Bind…](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY