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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
- Structure: A cyclohexane ring with an OH group on the first carbon and another OH group on the third carbon.
2. 
- Structure: A cyclohexane ring with an OH group on the first carbon and another OH group on the second carbon.
3. 
- Structure: A cyclohexane ring with an OH group on the first carbon and a double-bonded oxygen (carbonyl) on the third carbon.
**Explanation of the Reaction:**
Lithium Aluminium Hydride (LiAlH₄) is a strong reducing agent commonly used to reduce carbonyl compounds to alcohols. Here, the cyclic ketone is reduced to a diol (a molecule with two hydroxyl groups).
- LiAlH₄ and diethyl ether (Et₂O) is the initial step, wherein the ketone is reduced. The reaction is then quenched with water (H₂O) in the second step to replace the Al-O species with H-O (hydroxyl groups).
- The reaction primarily targets the carbonyl group, resulting in a reduction to a secondary alcohol.
The correct structure of the major organic product is depicted in the options given.
**Identifying the Major Organic Product:**
Based on the reduction mechanism described, the product lacking the carbonyl group and showing two hydroxyl (OH) groups will be more favorable.
**Select Your Answer:**
Choose the correct structural formula for the major organic product below:
1. 
2. 
3. 
(This transcription and solution aim to clarify and analyze the given chemical reaction and potential synthetic outcomes for educational purposes.)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F650638ef-17d9-4755-bd2c-89f9558934a8%2Ffd15bb42-4b7e-4cbe-b117-bdcad38705fe%2Fctprghg_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Question:**
What is the major organic product?
**Reaction Details:**
The starting material is a cyclic ketone. The reaction involves:
1. Treatment with LiAlH₄ (Lithium Aluminium Hydride) in Et₂O (Diethyl Ether).
2. Followed by addition of H₂O (Water).
**Options for the major organic product:**
1. 
- Structure: A cyclohexane ring with an OH group on the first carbon and another OH group on the third carbon.
2. 
- Structure: A cyclohexane ring with an OH group on the first carbon and another OH group on the second carbon.
3. 
- Structure: A cyclohexane ring with an OH group on the first carbon and a double-bonded oxygen (carbonyl) on the third carbon.
**Explanation of the Reaction:**
Lithium Aluminium Hydride (LiAlH₄) is a strong reducing agent commonly used to reduce carbonyl compounds to alcohols. Here, the cyclic ketone is reduced to a diol (a molecule with two hydroxyl groups).
- LiAlH₄ and diethyl ether (Et₂O) is the initial step, wherein the ketone is reduced. The reaction is then quenched with water (H₂O) in the second step to replace the Al-O species with H-O (hydroxyl groups).
- The reaction primarily targets the carbonyl group, resulting in a reduction to a secondary alcohol.
The correct structure of the major organic product is depicted in the options given.
**Identifying the Major Organic Product:**
Based on the reduction mechanism described, the product lacking the carbonyl group and showing two hydroxyl (OH) groups will be more favorable.
**Select Your Answer:**
Choose the correct structural formula for the major organic product below:
1. 
2. 
3. 
(This transcription and solution aim to clarify and analyze the given chemical reaction and potential synthetic outcomes for educational purposes.)
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