Kinetic vs Thermodynamic Product - 1,2 vs 1,4 Addition of HBr to 1,3- Butadiene | Summary and Q&A

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January 18, 2021
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Kinetic vs Thermodynamic Product - 1,2 vs 1,4 Addition of HBr to 1,3- Butadiene

TL;DR

This video discusses the different types of dienes and their reactions with hydrobromic acid, resulting in either kinetic or thermodynamic products.

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Key Insights

  • 🅰️ Dienes have different types, including conjugated, isolated, and cumulated.
  • ❓ Conjugated dienes react differently than isolated dienes due to resonance effects.
  • 💨 The kinetic product forms faster at low temperatures, while the thermodynamic product is the most stable and forms at high temperatures.
  • 💁 Alkene stability, determined by the number of attached alkyl groups, affects product formation.

Transcript

in this video we're going to talk about the 1 2 and the 1 4 addition products with dienes but let's begin our discussion with dienes so here is a typical alkene it has one double bond a diene is basically an alkene but with two double bonds now there's different types of dienes this particular diene is known as a conjugated diene the reason why it'... Read More

Questions & Answers

Q: What are the different types of dienes?

The different types of dienes are conjugated, isolated, and cumulated dienes. Conjugated dienes have alternating double and single bonds, isolated dienes have double bonds that are far apart, and cumulated dienes have double bonds close to each other.

Q: What is the difference between the kinetic and thermodynamic products?

The kinetic product forms faster at low temperatures and is less stable, while the thermodynamic product is the most stable and forms as the major product at high temperatures.

Q: How does alkene stability affect the product formation?

The more alkyl groups attached to the double-bonded carbons, the more stable the alkene. This stability helps identify the thermodynamic product.

Q: How does the reaction mechanism differ between low and high temperatures?

At low temperatures, the reaction is under kinetic control, with the diene acting as the nucleophile and HBr as the electrophile. At high temperatures, the reaction is reversible and follows thermodynamic control, resulting in the most stable alkene product.

Summary & Key Takeaways

  • Dienes are alkenes with two double bonds, and there are different types including conjugated, isolated, and cumulated dienes.

  • Conjugated dienes have special characteristics and react differently than isolated dienes.

  • When reacting one, three butadiene with hydrobromic acid, a low temperature produces the kinetic product (1,2 addition) while high temperature produces the thermodynamic product (1,4 addition).

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