1) Complete the following reactions by drawing in the starting materials, reagents, or products. Draw all major products where applicable. If no reaction will occur, write No RXN. HCL kot-Bv. A) B) Br <) >/ E) Br H₂O D) F) OH Cl2> H₂SO4

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Chapter1: Chemical Foundations
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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 Completion Exercise**

**Instructions:**
1. Complete the following reactions by drawing in the starting materials, reagents, or products. Draw all major products where applicable. If no reaction will occur, write 'No RXN'.

### Reactions:

**A)**
Starting Material: 
- A compound with a Bromine atom (Br) attached to the second carbon of a-butyl chain.
  
Reagent: 
- \( KOT-Bu \) (Potassium tert-butoxide)

**B)**
Starting Material:
- A compound with an alkene at the end of the chain.

Reagent: 
- \( HCl \) (Hydrochloric acid)

**C)**
Starting Material:
- An alkyne with one ethyl group attached to the second carbon of a hexane chain.

Reagent:
- [No reagent is provided, implies that you need to figure out possible reagents and products from given starting material]

**D)**
Starting Material:
- Benzene ring.

Reagent:
- \( Cl_2 \) (Chlorine)

**E)**
Starting Material:
- Benzene ring.

Reagent: 
- \( Br_2 \) (Bromine) and \( H_2O \) (Water)

**F)**
Starting Material:
- A secondary alcohol.

Reagent:
- \( H_2SO_4 \) (Sulfuric acid) with heat.


### Diagrams Explanation:

- **Diagram A:** It shows a five-carbon chain with a bromine (Br) attached to the second carbon (starting material), and the reagent \( KOT-Bu \) is indicated. 
- **Diagram B:** Illustrates a three-carbon chain with a terminal double bond, and the reagent \( HCl \) is indicated.
- **Diagram C:** Depicts an alkyne with substituents leading into a cyclohexane structure, implying a transformation or additional steps.
- **Diagram D:** Shows a benzene ring with \( Cl_2 \) as the reactive agent.
- **Diagram E:** Displays benzene, suggesting an electrophilic addition reaction with bromine in aqueous media.
- **Diagram F:** Presents a secondary alcohol subjected to dehydration conditions using \( H_2SO_4 \) and heat.

Each question represents a fundamental organic reaction, requiring an understanding of reaction mechanisms and the ability to predict the major product. Use these diagrams to sketch out
Transcribed Image Text:**Organic Chemistry Reaction Completion Exercise** **Instructions:** 1. Complete the following reactions by drawing in the starting materials, reagents, or products. Draw all major products where applicable. If no reaction will occur, write 'No RXN'. ### Reactions: **A)** Starting Material: - A compound with a Bromine atom (Br) attached to the second carbon of a-butyl chain. Reagent: - \( KOT-Bu \) (Potassium tert-butoxide) **B)** Starting Material: - A compound with an alkene at the end of the chain. Reagent: - \( HCl \) (Hydrochloric acid) **C)** Starting Material: - An alkyne with one ethyl group attached to the second carbon of a hexane chain. Reagent: - [No reagent is provided, implies that you need to figure out possible reagents and products from given starting material] **D)** Starting Material: - Benzene ring. Reagent: - \( Cl_2 \) (Chlorine) **E)** Starting Material: - Benzene ring. Reagent: - \( Br_2 \) (Bromine) and \( H_2O \) (Water) **F)** Starting Material: - A secondary alcohol. Reagent: - \( H_2SO_4 \) (Sulfuric acid) with heat. ### Diagrams Explanation: - **Diagram A:** It shows a five-carbon chain with a bromine (Br) attached to the second carbon (starting material), and the reagent \( KOT-Bu \) is indicated. - **Diagram B:** Illustrates a three-carbon chain with a terminal double bond, and the reagent \( HCl \) is indicated. - **Diagram C:** Depicts an alkyne with substituents leading into a cyclohexane structure, implying a transformation or additional steps. - **Diagram D:** Shows a benzene ring with \( Cl_2 \) as the reactive agent. - **Diagram E:** Displays benzene, suggesting an electrophilic addition reaction with bromine in aqueous media. - **Diagram F:** Presents a secondary alcohol subjected to dehydration conditions using \( H_2SO_4 \) and heat. Each question represents a fundamental organic reaction, requiring an understanding of reaction mechanisms and the ability to predict the major product. Use these diagrams to sketch out
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