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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Name of reaction, what would happen if you used methanol instead of benzene

Transcribed Image Text:The image shows a chemical reaction involving a cyclohexane derivative.
**Starting Material:**
- A cyclohexane ring with an attached hydroxyl group (OH) and a carboxylic acid group (CO₂H).
**Reaction Conditions:**
- Acid-catalyzed reaction (H⁺).
- Solvent: Benzene.
**Product Formation:**
- The cyclohexane derivative is converted into a lactone, a cyclic ester (shown with a carbonyl group within the ring).
- Water (H₂O) is released as a byproduct.
**Reaction Process:**
The reaction involves the dehydration of a hydroxy acid to form a lactone, facilitated by acid catalysis in a benzene solvent. The transformation involves the formation of a cyclic ester, with the removal of a water molecule.
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