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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![### Question 16:
Carefully draw the **two** enol tautomers of the following compound and **circle** the one that is more stable.
![Structural formula of a compound](data:image/png;base64,...)
---
The image shows the chemical structure of a compound consisting of a benzene ring attached to an acetyl group. The task requires drawing the two enol tautomers of this compound and identifying which one is more stable. To do this, the keto form will need to be converted into its enol forms, showing the migration of a hydrogen atom and the shift of a double bond. The more stable enol tautomer typically has resonance stabilization or stronger hydrogen bonding, factors to consider when circling the more stable form.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Faa58f639-8371-4224-bff2-3cca37cc0941%2Fa727e843-1a06-481f-b9e4-0a59188c1708%2F4rdv5rf_processed.png&w=3840&q=75)
Transcribed Image Text:### Question 16:
Carefully draw the **two** enol tautomers of the following compound and **circle** the one that is more stable.
![Structural formula of a compound](data:image/png;base64,...)
---
The image shows the chemical structure of a compound consisting of a benzene ring attached to an acetyl group. The task requires drawing the two enol tautomers of this compound and identifying which one is more stable. To do this, the keto form will need to be converted into its enol forms, showing the migration of a hydrogen atom and the shift of a double bond. The more stable enol tautomer typically has resonance stabilization or stronger hydrogen bonding, factors to consider when circling the more stable form.
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