4. Provide the reagents (at the reaction arrows, use 1).... 2).... if more than one step is needed) that synthesize the indicated carboxylic acids. + CHCI3 он + он он Br он + NH HO.
4. Provide the reagents (at the reaction arrows, use 1).... 2).... if more than one step is needed) that synthesize the indicated carboxylic acids. + CHCI3 он + он он Br он + NH HO.
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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![### Problem 4: Synthesis of Indicated Carboxylic Acids
**Objective:**
Provide the reagents (at the reaction arrows, use 1).... 2).... if more than one step is needed) that synthesize the indicated carboxylic acids.
**Given:**
Four different organic compounds are provided as starting materials, each requiring conversion to a specific carboxylic acid. At each reaction arrow, the correct reagents must be provided.
### Reactions
1. **First Reaction:**
- **Starting Material:** Pentanal
- **Target Product:** Pentanoic acid and chloroform (CHCl₃)
2. **Second Reaction:**
- **Starting Material:** Ethyl acetate
- **Target Product:** Acetic acid and ethanol
3. **Third Reaction:**
- **Starting Material:** 1-Bromo-1-phenylethane
- **Target Product:** Benzoic acid
4. **Fourth Reaction:**
- **Starting Material:** 3-Cyanopropene
- **Target Product:** Butanoic acid and ammonium ion (NH₄⁺)
### Missing Reagents (to be identified):
1. **Reagents for Pentanal to Pentanoic Acid and Chloroform:**
- Reagent 1: TBD
- Reagent 2: TBD
2. **Reagents for Ethyl acetate to Acetic Acid and Ethanol:**
- Reagent 1: TBD
- Reagent 2: TBD
3. **Reagents for 1-Bromo-1-phenylethane to Benzoic Acid:**
- Reagent 1: TBD
- Reagent 2: TBD
4. **Reagents for 3-Cyanopropene to Butanoic Acid and NH₄⁺:**
- Reagent 1: TBD
- Reagent 2: TBD
**Explanation of Diagram:**
Each reaction sequence is represented as a set of organic chemical structures. The starting material is on the left side, and the target products are on the right side, connected by an arrow. The arrow includes a rectangular box where the required reagents need to be indicated.
**Note:** Students should carefully identify the reagents required to achieve the target product from the given starting material, keeping in mind standard organic chemistry](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fff015db4-0da8-42fc-9d60-01a672218c35%2F10fddd99-95a5-4b69-bd1d-b93d6bb9a0ed%2Fklpqyx_processed.jpeg&w=3840&q=75)
Transcribed Image Text:### Problem 4: Synthesis of Indicated Carboxylic Acids
**Objective:**
Provide the reagents (at the reaction arrows, use 1).... 2).... if more than one step is needed) that synthesize the indicated carboxylic acids.
**Given:**
Four different organic compounds are provided as starting materials, each requiring conversion to a specific carboxylic acid. At each reaction arrow, the correct reagents must be provided.
### Reactions
1. **First Reaction:**
- **Starting Material:** Pentanal
- **Target Product:** Pentanoic acid and chloroform (CHCl₃)
2. **Second Reaction:**
- **Starting Material:** Ethyl acetate
- **Target Product:** Acetic acid and ethanol
3. **Third Reaction:**
- **Starting Material:** 1-Bromo-1-phenylethane
- **Target Product:** Benzoic acid
4. **Fourth Reaction:**
- **Starting Material:** 3-Cyanopropene
- **Target Product:** Butanoic acid and ammonium ion (NH₄⁺)
### Missing Reagents (to be identified):
1. **Reagents for Pentanal to Pentanoic Acid and Chloroform:**
- Reagent 1: TBD
- Reagent 2: TBD
2. **Reagents for Ethyl acetate to Acetic Acid and Ethanol:**
- Reagent 1: TBD
- Reagent 2: TBD
3. **Reagents for 1-Bromo-1-phenylethane to Benzoic Acid:**
- Reagent 1: TBD
- Reagent 2: TBD
4. **Reagents for 3-Cyanopropene to Butanoic Acid and NH₄⁺:**
- Reagent 1: TBD
- Reagent 2: TBD
**Explanation of Diagram:**
Each reaction sequence is represented as a set of organic chemical structures. The starting material is on the left side, and the target products are on the right side, connected by an arrow. The arrow includes a rectangular box where the required reagents need to be indicated.
**Note:** Students should carefully identify the reagents required to achieve the target product from the given starting material, keeping in mind standard organic chemistry
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