Draw the resonance contributors for the species/molecules shown in the boxes below. Then, indicate which species (if any) is the MAJOR contributor towards the resonance hybrid (most stable).
Draw the resonance contributors for the species/molecules shown in the boxes below. Then, indicate which species (if any) is the MAJOR contributor towards the resonance hybrid (most stable).
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
Draw the resonance contributors for the species/molecules shown in the boxes below. Then, indicate which species (if any) is the MAJOR contributor towards the resonance hybrid (most stable).
![**1. Resonance Practice!**
**Instructions:** Draw the resonance contributors for the species/molecules shown in the boxes below. Then, indicate which species (if any) is the MAJOR contributor towards the resonance hybrid (most stable).
---
**a.**
Structure: A molecule with a positively charged oxygen atom at one end, connected to a sequence of single and double bonds extending through a carbon chain.
Boxes: Three empty boxes are provided to draw resonance structures with double-headed arrows between them.
---
**b.**
Structure: A molecule showing an amide group (O=C-NH) adjacent to an alkene group.
Boxes: Two empty boxes are provided with a double-headed arrow between them for drawing resonance structures.
---
**c.**
Structure: A cyclic molecule with an oxygen atom double-bonded to a carbon atom, displaying a negative charge on an oxygen atom outside the ring.
Boxes: Three empty boxes are provided with double-headed arrows between them to illustrate possible resonance structures.
---
Fill in the boxes with resonance forms, and identify the most stable (major) contributor among them.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F9fa0ca06-dd60-4896-86b5-5c6179a72eaa%2Fafdc2072-fd1c-4fb2-8413-c68f1bb86e31%2F19znl77_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**1. Resonance Practice!**
**Instructions:** Draw the resonance contributors for the species/molecules shown in the boxes below. Then, indicate which species (if any) is the MAJOR contributor towards the resonance hybrid (most stable).
---
**a.**
Structure: A molecule with a positively charged oxygen atom at one end, connected to a sequence of single and double bonds extending through a carbon chain.
Boxes: Three empty boxes are provided to draw resonance structures with double-headed arrows between them.
---
**b.**
Structure: A molecule showing an amide group (O=C-NH) adjacent to an alkene group.
Boxes: Two empty boxes are provided with a double-headed arrow between them for drawing resonance structures.
---
**c.**
Structure: A cyclic molecule with an oxygen atom double-bonded to a carbon atom, displaying a negative charge on an oxygen atom outside the ring.
Boxes: Three empty boxes are provided with double-headed arrows between them to illustrate possible resonance structures.
---
Fill in the boxes with resonance forms, and identify the most stable (major) contributor among them.
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)
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