Complete the following reactions. Write in Stereochemistry where relevant. Write No RXN if no reaction will occur. 1) of PCC ₂ рсс, 2) 1)LAH 2) 4,06 песна 3) 4) i OH
Complete the following reactions. Write in Stereochemistry where relevant. Write No RXN if no reaction will occur. 1) of PCC ₂ рсс, 2) 1)LAH 2) 4,06 песна 3) 4) i OH
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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### Organic Chemistry Reaction Exercises
Complete the following reactions. Write in stereochemistry where relevant. Write "No RXN" if no reaction will occur.
#### 1)
**Reactant:** Cyclohexanol
**Reagent:** PCC (Pyridinium Chlorochromate)
![Cyclohexanol to Cyclohexanone](https://via.placeholder.com/100)
**Product:** Cyclohexanone
_Explanation: Oxidation of alcohol to ketone using PCC._
#### 2)
**Reactant:** Cyclohexanone
**Reagent:**
1) LAH (Lithium Aluminium Hydride)
2) H₂O
![Cyclohexanone to Cyclohexanol](https://via.placeholder.com/100)
**Product:** Cyclohexanol
_Explanation: Reduction of ketone to alcohol using LAH followed by hydrolysis._
#### 3)
**Reactant:** 4-hydroxybutanal
**Reagent:** PCC
![4-Hydroxybutanal to 4-Oxo-butanal](https://via.placeholder.com/100)
**Product:** 4-Oxo-butanal
_Explanation: Oxidation of primary alcohol to aldehyde using PCC._
#### 4)
**Reactant:** 3-hydroxy-2-methylpropionic acid
**Reagent:** _none_ (Product shown)
![3-Hydroxy-2-methylpropionic acid to 3-Oxo-2-methylpropionic acid](https://via.placeholder.com/100)
**Product:** 3-Oxo-2-methylpropionic acid
_Explanation: The 3-hydroxy-2-methylpropionic acid undergoes oxidation of the hydroxyl group to a keto group._
---
**Note:** Ensure to balance the equations if required and practice drawing the structures accurately.
**Graphs/Diagrams Explanation:** No additional graphs or diagrams being present in this image.
---](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F47f16b03-5eea-43fc-9b52-7dcc57452af9%2F2a126dc9-3d36-488a-ae78-65ca118170fc%2F1f90y8_processed.jpeg&w=3840&q=75)
Transcribed Image Text:---
### Organic Chemistry Reaction Exercises
Complete the following reactions. Write in stereochemistry where relevant. Write "No RXN" if no reaction will occur.
#### 1)
**Reactant:** Cyclohexanol
**Reagent:** PCC (Pyridinium Chlorochromate)
![Cyclohexanol to Cyclohexanone](https://via.placeholder.com/100)
**Product:** Cyclohexanone
_Explanation: Oxidation of alcohol to ketone using PCC._
#### 2)
**Reactant:** Cyclohexanone
**Reagent:**
1) LAH (Lithium Aluminium Hydride)
2) H₂O
![Cyclohexanone to Cyclohexanol](https://via.placeholder.com/100)
**Product:** Cyclohexanol
_Explanation: Reduction of ketone to alcohol using LAH followed by hydrolysis._
#### 3)
**Reactant:** 4-hydroxybutanal
**Reagent:** PCC
![4-Hydroxybutanal to 4-Oxo-butanal](https://via.placeholder.com/100)
**Product:** 4-Oxo-butanal
_Explanation: Oxidation of primary alcohol to aldehyde using PCC._
#### 4)
**Reactant:** 3-hydroxy-2-methylpropionic acid
**Reagent:** _none_ (Product shown)
![3-Hydroxy-2-methylpropionic acid to 3-Oxo-2-methylpropionic acid](https://via.placeholder.com/100)
**Product:** 3-Oxo-2-methylpropionic acid
_Explanation: The 3-hydroxy-2-methylpropionic acid undergoes oxidation of the hydroxyl group to a keto group._
---
**Note:** Ensure to balance the equations if required and practice drawing the structures accurately.
**Graphs/Diagrams Explanation:** No additional graphs or diagrams being present in this image.
---
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