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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![**Title: Chemical Reaction Pathways: Alkynes to Carboxylic Acids**
**Instruction:**
Draw the starting alkyne that would lead to the following two products under these conditions.
**Reaction Overview:**
1. **Reagents:**
- Ozone (O₃)
- Acetic acid (HOAc)
2. **Products Formed:**
- The first product is a carboxylic acid with a three-carbon chain and a terminal hydroxyl group attached to a carbonyl group.
- The second product is a two-carbon carboxylic acid with a hydroxyl group attached to a carbonyl carbon.
**Visual Explanation:**
- There is a diagram depicting a box labeled "Select to Draw," indicating where students should input their structures.
- A vertical arrow points downward from the drawing box to indicate the direction of the reaction.
- Beneath the conditions (O₃ and HOAc) are chemical structures of the resulting products: one has three carbons, and the other has two carbons, both with carboxylic acid functional groups.
**Conclusion:**
This exercise involves identifying the correct alkyne that, when reacted with ozone and acetic acid, would yield the specified carboxylic acids. Students are encouraged to consider the oxidative cleavage mechanism involved in the reaction of alkynes.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F8f950e16-ff9d-4c3e-b6ed-db2ea86994c5%2F76e026d1-819c-453f-a98e-0f0a4e0fe1ee%2Fvzxmla_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Title: Chemical Reaction Pathways: Alkynes to Carboxylic Acids**
**Instruction:**
Draw the starting alkyne that would lead to the following two products under these conditions.
**Reaction Overview:**
1. **Reagents:**
- Ozone (O₃)
- Acetic acid (HOAc)
2. **Products Formed:**
- The first product is a carboxylic acid with a three-carbon chain and a terminal hydroxyl group attached to a carbonyl group.
- The second product is a two-carbon carboxylic acid with a hydroxyl group attached to a carbonyl carbon.
**Visual Explanation:**
- There is a diagram depicting a box labeled "Select to Draw," indicating where students should input their structures.
- A vertical arrow points downward from the drawing box to indicate the direction of the reaction.
- Beneath the conditions (O₃ and HOAc) are chemical structures of the resulting products: one has three carbons, and the other has two carbons, both with carboxylic acid functional groups.
**Conclusion:**
This exercise involves identifying the correct alkyne that, when reacted with ozone and acetic acid, would yield the specified carboxylic acids. Students are encouraged to consider the oxidative cleavage mechanism involved in the reaction of alkynes.
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