Page 23 Flashcards

1
Q

Why does the E2 reaction rate increase with increasing alkyl substitution?

A

A: Alkyl substituents stabilize the transition state of the reaction by stabilizing the partially formed double bond, which lowers the activation energy (E_a).

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2
Q

Flashcard 2
Q: What happens in the transition state of an E2 reaction?

A

A: The double bond is partially formed, and the proton is being removed by the base while the leaving group departs simultaneously.

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3
Q

How do alkyl groups stabilize the transition state in an E2 reaction?

A

A: Alkyl groups donate electron density through hyperconjugation, stabilizing the partially formed double bond.

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4
Q

What is the effect of stabilizing the transition state in E2 mechanisms?

A

A: It reduces the energy barrier for the reaction, increasing the rate of the reaction.

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5
Q

What is shown in the diagram?

A

A: The transition state of an E2 reaction with an alkoxide ( -OR ) as the base. The proton is being abstracted, the leaving group departs, and the double bond begins to form.

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