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Identify compound P, Q, R and S in the following reactions: OH D. C2, H20 Sebatian P Compound P a) CH3COCI Sebatian Q Compound Q AIC b) OH Sebatian R Compound R 1. LIAIH4, THF 2. H;0* c)

Identify compound P, Q, R and S in the following reactions: OH D. C2, H20 Sebatian P Compound P a) CH3COCI Sebatian Q Compound Q AIC b) OH Sebatian R Compound R 1. LIAIH4, THF 2. H;0* c)

Chemistry for Today: General, Organic, and Biochemistry
Chemistry for Today: General, Organic, and Biochemistry
9th Edition
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Chapter14: Aldehydes And Ketones
Section: Chapter Questions
Problem 14.55E: The addition of water to aldehydes and ketones occurs rapidly, although it is not thermodynamically...
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### Organic Chemistry Reaction Pathways In this section, we investigate the identification of compounds P, Q, R, and S through a series of organic reactions. The structures and reagents used are given as part of the reaction pathways. #### Reaction Pathways: 1. **Reaction a:** - Starting from: ``` Sebatian P Compound P: ![Structure of a cyclohexanol derivative](<Structure>) ``` - Reaction conditions: ``` Cl2, H2O ``` - Product: ``` ![Structure of chlorocyclohexanol derivative](<Structure>) ``` 2. **Reaction b:** - Starting from: ``` ![Structure of a ketone with a benzene ring](<Structure>) ``` - Reaction conditions: ``` CH3COCl, AlCl3 ``` - Product: ``` Sebatian Q Compound Q: ![Structure of a corresponding acylated benzene derivative](<Structure>) ``` 3. **Reaction c:** - Starting from: ``` ![Structure of a ketone with tert-butyl group](<Structure>) ``` - Reaction conditions: ``` 1. LiAlH4, THF 2. H3O+ ``` - Product: ``` Sebatian R Compound R: ![Structure of a reduced alcohol](<Structure>) ``` 4. **Reaction d:** - Starting from: ``` ![Structure of a cyclic ketone with alcohol group](<Structure>) ``` - Reaction conditions: ``` Sebatian S Compound S: ![Structure of a cyclic ketone with an added group](<Structure>) ``` #### Detailed Descriptions: 1. **Graph/Diagram for Reaction a:** - The starting material for compound P is an organic molecule featuring a cyclohexane ring with a hydroxyl and ether linkage. - The product is a chlorocyclohexanol after the reaction with chlorine gas (Cl2) in the presence of water. 2. **Graph/Diagram for Reaction b:** - The starting material is a methyl-benzene derivative (commonly known as acetophenone). - Using Friedel
Transcribed Image Text:### Organic Chemistry Reaction Pathways In this section, we investigate the identification of compounds P, Q, R, and S through a series of organic reactions. The structures and reagents used are given as part of the reaction pathways. #### Reaction Pathways: 1. **Reaction a:** - Starting from: ``` Sebatian P Compound P: ![Structure of a cyclohexanol derivative](<Structure>) ``` - Reaction conditions: ``` Cl2, H2O ``` - Product: ``` ![Structure of chlorocyclohexanol derivative](<Structure>) ``` 2. **Reaction b:** - Starting from: ``` ![Structure of a ketone with a benzene ring](<Structure>) ``` - Reaction conditions: ``` CH3COCl, AlCl3 ``` - Product: ``` Sebatian Q Compound Q: ![Structure of a corresponding acylated benzene derivative](<Structure>) ``` 3. **Reaction c:** - Starting from: ``` ![Structure of a ketone with tert-butyl group](<Structure>) ``` - Reaction conditions: ``` 1. LiAlH4, THF 2. H3O+ ``` - Product: ``` Sebatian R Compound R: ![Structure of a reduced alcohol](<Structure>) ``` 4. **Reaction d:** - Starting from: ``` ![Structure of a cyclic ketone with alcohol group](<Structure>) ``` - Reaction conditions: ``` Sebatian S Compound S: ![Structure of a cyclic ketone with an added group](<Structure>) ``` #### Detailed Descriptions: 1. **Graph/Diagram for Reaction a:** - The starting material for compound P is an organic molecule featuring a cyclohexane ring with a hydroxyl and ether linkage. - The product is a chlorocyclohexanol after the reaction with chlorine gas (Cl2) in the presence of water. 2. **Graph/Diagram for Reaction b:** - The starting material is a methyl-benzene derivative (commonly known as acetophenone). - Using Friedel
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