Draw the two possible products formed when 1,3- butadiene reacts with this acid. Do not include any byproducts formed.

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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**Title: Reaction of 1,3-Butadiene with Acid**

**Description:**
In this exercise, you are required to draw the two possible products formed when 1,3-butadiene reacts with an acid, denoted as H₃O⁺ (one equivalent). Please exclude any byproducts from your drawings.

**Chemical Reactions:**

- **Reactant:** 1,3-Butadiene

- **Reagent:** Acid (H₃O⁺, 1 equivalent)

**Instructions:**

1. **Draw the Reaction Products:**
   - There are two main products formed in this reaction:
     - The **1,2-addition product** (indicated as "Drawing" in a red dashed box).
     - The **1,4-addition product** (indicated as "Draw 1,4 Product" in a black dashed box).

**Diagrams:**

- The diagram shows the structure of 1,3-butadiene at the top, followed by an arrow indicating the reaction direction with H₃O⁺.
- Two spaces are provided to draw the respective reaction products.

**Objective:**
Understand and illustrate the mechanism by which 1,3-butadiene can undergo electrophilic addition with an acid, forming two possible addition products involving different bond positions.
Transcribed Image Text:**Title: Reaction of 1,3-Butadiene with Acid** **Description:** In this exercise, you are required to draw the two possible products formed when 1,3-butadiene reacts with an acid, denoted as H₃O⁺ (one equivalent). Please exclude any byproducts from your drawings. **Chemical Reactions:** - **Reactant:** 1,3-Butadiene - **Reagent:** Acid (H₃O⁺, 1 equivalent) **Instructions:** 1. **Draw the Reaction Products:** - There are two main products formed in this reaction: - The **1,2-addition product** (indicated as "Drawing" in a red dashed box). - The **1,4-addition product** (indicated as "Draw 1,4 Product" in a black dashed box). **Diagrams:** - The diagram shows the structure of 1,3-butadiene at the top, followed by an arrow indicating the reaction direction with H₃O⁺. - Two spaces are provided to draw the respective reaction products. **Objective:** Understand and illustrate the mechanism by which 1,3-butadiene can undergo electrophilic addition with an acid, forming two possible addition products involving different bond positions.
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