1. Mgº (metal) b. 2. HCHO -Br 3. H₂O+ i. Does this reaction have any regiocontrol (yes or no)? 1. Liº (metal) C. 2. Cul, -78°C 3. i. What is the name of this reaction (one word answer)? d. MeOH heat i. What is the mechanism of this reaction (SN1, SN2, E2, E1)? ii. What is the regiocontrol of this reaction? < Previous Next >

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 Matching Exercise**

**Introduction:**
Below you will find twelve (12) reaction products (labeled product 1, product 2, etc.), but you will only find five (5) reaction schemes. Your job is to match the reaction scheme with the correct product. Simply fill in the blank with the product number (i.e., 1, 2, 3, etc.). Then, answer any additional questions regarding the reaction scheme(s).

**Reaction Products:**

1. **Product 1:**
   - Structural Formula: Cyclohexane ring with a bromine (Br) substituent.

2. **Product 2:**
   - Structural Formula: Cyclohexane ring with a hydroxyl (OH) substituent.

3. **Product 3:**
   - Structural Formula: Isopropyl group with a methoxy (OMe) substituent at the end.

4. **Product 4:**
   - Structural Formula: Benzene ring fused to a cyclohexane with a sec-butyl group.

5. **Product 5:**
   - Structural Formula: Cyclohexane ring with a carboxylic acid (CO₂H) substituent and a methyl group.

6. **Product 6:**
   - Structural Formula: Cyclohexane ring with an ethyl group and a propyl group (1,3-dipropylcyclohexane).

7. **Product 7:**
   - Structural Formula: Isopropyl group with a methoxy (OMe) substituent at the end (similar to Product 3 but with different stereochemistry).

8. **Product 8:**
   - Structural Formula: Cyclohexane ring with a bromine (Br) substituent and a carboxylic acid (CO₂H) substituent.

9. **Product 9:**
   - Structural Formula: Isopropyl group with a methoxy (OMe) substituent at the end.

10. **Product 10:**
    - Structural Formula: Cyclohexane ring with a bromine (Br) substituent and a propyl group.

11. **Product 11:**
    - Structural Formula: Benzene ring fused to a cyclohexane with a butyl group.

12. **Product 12:**
    - Structural Formula: Cyclohexane ring with a carboxylic acid
Transcribed Image Text:**Organic Chemistry Reaction Matching Exercise** **Introduction:** Below you will find twelve (12) reaction products (labeled product 1, product 2, etc.), but you will only find five (5) reaction schemes. Your job is to match the reaction scheme with the correct product. Simply fill in the blank with the product number (i.e., 1, 2, 3, etc.). Then, answer any additional questions regarding the reaction scheme(s). **Reaction Products:** 1. **Product 1:** - Structural Formula: Cyclohexane ring with a bromine (Br) substituent. 2. **Product 2:** - Structural Formula: Cyclohexane ring with a hydroxyl (OH) substituent. 3. **Product 3:** - Structural Formula: Isopropyl group with a methoxy (OMe) substituent at the end. 4. **Product 4:** - Structural Formula: Benzene ring fused to a cyclohexane with a sec-butyl group. 5. **Product 5:** - Structural Formula: Cyclohexane ring with a carboxylic acid (CO₂H) substituent and a methyl group. 6. **Product 6:** - Structural Formula: Cyclohexane ring with an ethyl group and a propyl group (1,3-dipropylcyclohexane). 7. **Product 7:** - Structural Formula: Isopropyl group with a methoxy (OMe) substituent at the end (similar to Product 3 but with different stereochemistry). 8. **Product 8:** - Structural Formula: Cyclohexane ring with a bromine (Br) substituent and a carboxylic acid (CO₂H) substituent. 9. **Product 9:** - Structural Formula: Isopropyl group with a methoxy (OMe) substituent at the end. 10. **Product 10:** - Structural Formula: Cyclohexane ring with a bromine (Br) substituent and a propyl group. 11. **Product 11:** - Structural Formula: Benzene ring fused to a cyclohexane with a butyl group. 12. **Product 12:** - Structural Formula: Cyclohexane ring with a carboxylic acid
## Organic Chemistry Reaction Mechanisms

**b. Reaction**

Starting Material:  
![Starting Material](https://latex.codecogs.com/svg.latex?\text{Cyclohexane%20ring%20with%20a%20bromo%20%28Br%29%20group}.)

Reagents:  
1. Mg° (metal)  
2. HCHO  
3. H₃O⁺  

---  
i. **Question:** Does this reaction have any regiocontrol (yes or no)?  
**Answer:** (Input expected)

**c. Reaction**

Starting Material:  
![Starting Material](https://latex.codecogs.com/svg.latex?\text{Alkyl%20group%20attached%20to%20a%20leaving%20group}.)

Reagents:  
1. Li° (metal)  
2. CuI, -78°C  
3. ![Benzene](https://latex.codecogs.com/svg.latex?\text{Benzene%20ring}.)

---  
i. **Question:** What is the name of this reaction (one word answer)?  
**Answer:** (Input expected)

**d. Reaction**

Starting Material:  
![Starting Material](https://latex.codecogs.com/svg.latex?\text{3-Bromo-2,2-Dimethylpentane}.)

Reagent:  
MeOH, heat  

---  
i. **Question:** What is the mechanism of this reaction (SN1, SN2, E2, E1)?  
**Answer:** (Input expected)

ii. **Question:** What is the regiocontrol of this reaction?  
**Answer:** (Input expected)

**Navigation:**  
![Previous Button](https://latex.codecogs.com/svg.latex?\text{<%20Previous})  ![Next Button](https://latex.codecogs.com/svg.latex?\text{Next%20>})

---

Each reaction above involves different reagents and conditions, which influence the products formed through distinct mechanisms. When studying these reactions, focus on understanding the role of each reagent and the type of reaction mechanism involved (e.g. substitution or elimination).
Transcribed Image Text:## Organic Chemistry Reaction Mechanisms **b. Reaction** Starting Material: ![Starting Material](https://latex.codecogs.com/svg.latex?\text{Cyclohexane%20ring%20with%20a%20bromo%20%28Br%29%20group}.) Reagents: 1. Mg° (metal) 2. HCHO 3. H₃O⁺ --- i. **Question:** Does this reaction have any regiocontrol (yes or no)? **Answer:** (Input expected) **c. Reaction** Starting Material: ![Starting Material](https://latex.codecogs.com/svg.latex?\text{Alkyl%20group%20attached%20to%20a%20leaving%20group}.) Reagents: 1. Li° (metal) 2. CuI, -78°C 3. ![Benzene](https://latex.codecogs.com/svg.latex?\text{Benzene%20ring}.) --- i. **Question:** What is the name of this reaction (one word answer)? **Answer:** (Input expected) **d. Reaction** Starting Material: ![Starting Material](https://latex.codecogs.com/svg.latex?\text{3-Bromo-2,2-Dimethylpentane}.) Reagent: MeOH, heat --- i. **Question:** What is the mechanism of this reaction (SN1, SN2, E2, E1)? **Answer:** (Input expected) ii. **Question:** What is the regiocontrol of this reaction? **Answer:** (Input expected) **Navigation:** ![Previous Button](https://latex.codecogs.com/svg.latex?\text{<%20Previous}) ![Next Button](https://latex.codecogs.com/svg.latex?\text{Next%20>}) --- Each reaction above involves different reagents and conditions, which influence the products formed through distinct mechanisms. When studying these reactions, focus on understanding the role of each reagent and the type of reaction mechanism involved (e.g. substitution or elimination).
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