Draw the product that could be formed when 1,3- butadiene reacts with ethene.

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
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**Transcribed Content for Educational Website**

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**Challenge: Reaction of 1,3-Butadiene with Ethene**

**Task:** Draw the product that could be formed when 1,3-butadiene reacts with ethene.

**Diagram Explanation:**

The image depicts the reactants involved in the Diels-Alder reaction: 

1. **1,3-Butadiene Structure:** 
   - A four-carbon chain with two alternating double bonds. The double bonds are shown as lines between carbon atoms.

2. **Ethene Structure:**
   - A two-carbon compound with a single double bond.

**Reaction Indication:**
- An arrow points downward, suggesting a chemical reaction that leads to the formation of a new product.

This reaction typically results in a cyclic compound through a [4+2] cycloaddition process, where electrons in the π-bonds of the conjugated diene (1,3-butadiene) interact with the π-bonds of the dienophile (ethene).

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**Further Exploration:**

Students are encouraged to draw the possible cyclic product from this reaction based on the structures provided. This exercise helps in understanding concepts related to organic reactions, functional groups, and molecular geometry.
Transcribed Image Text:**Transcribed Content for Educational Website** --- **Challenge: Reaction of 1,3-Butadiene with Ethene** **Task:** Draw the product that could be formed when 1,3-butadiene reacts with ethene. **Diagram Explanation:** The image depicts the reactants involved in the Diels-Alder reaction: 1. **1,3-Butadiene Structure:** - A four-carbon chain with two alternating double bonds. The double bonds are shown as lines between carbon atoms. 2. **Ethene Structure:** - A two-carbon compound with a single double bond. **Reaction Indication:** - An arrow points downward, suggesting a chemical reaction that leads to the formation of a new product. This reaction typically results in a cyclic compound through a [4+2] cycloaddition process, where electrons in the π-bonds of the conjugated diene (1,3-butadiene) interact with the π-bonds of the dienophile (ethene). --- **Further Exploration:** Students are encouraged to draw the possible cyclic product from this reaction based on the structures provided. This exercise helps in understanding concepts related to organic reactions, functional groups, and molecular geometry.
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