Review: Which of the following contribute to the favorablilty of the following elimination? CH₂00 H Ph L.H CI H · X ·a° + Ph CH₂OH + Hint: the "favorability" of a reaction has nothing to do with the speed of a reaction. When I ask about favorability, I am asking about thermodynamic considerations rather than kinetic ones. O The unstable charge on the base lowers the activation energy of the reaction. Formation of three products from two reactants is entropically favorable The charge formed on the leaving group is more stable than the charge on the base. The pi bond formed in the product is more stable than the sigma bond broken in the reactant

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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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**Review: Which of the following contribute to the favorability of the following elimination?**

**Chemical Reaction Diagram:**

- Reactants: 
  - Methoxide ion (CH₃O⁻)
  - 1-chloro-1-phenylethane (depicted with the Cl, Ph, and H groups)

- Products: 
  - Methanol (CH₃OH)
  - Phenylethene (PhCH=CH₂)
  - Chloride ion (Cl⁻)

**Hint:**
The "favorability" of a reaction has nothing to do with the speed of a reaction. When I ask about favorability, I am asking about thermodynamic considerations rather than kinetic ones.

**Options:**
- [ ] The unstable charge on the base lowers the activation energy of the reaction.
- [ ] Formation of three products from two reactants is entropically favorable.
- [ ] The charge formed on the leaving group is more stable than the charge on the base.
- [ ] The pi bond formed in the product is more stable than the sigma bond broken in the reactant.
Transcribed Image Text:**Review: Which of the following contribute to the favorability of the following elimination?** **Chemical Reaction Diagram:** - Reactants: - Methoxide ion (CH₃O⁻) - 1-chloro-1-phenylethane (depicted with the Cl, Ph, and H groups) - Products: - Methanol (CH₃OH) - Phenylethene (PhCH=CH₂) - Chloride ion (Cl⁻) **Hint:** The "favorability" of a reaction has nothing to do with the speed of a reaction. When I ask about favorability, I am asking about thermodynamic considerations rather than kinetic ones. **Options:** - [ ] The unstable charge on the base lowers the activation energy of the reaction. - [ ] Formation of three products from two reactants is entropically favorable. - [ ] The charge formed on the leaving group is more stable than the charge on the base. - [ ] The pi bond formed in the product is more stable than the sigma bond broken in the reactant.
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