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

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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.

---
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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