Page 33 Flashcards

1
Q

What is the first step common to both Sₙ1 and E1 reactions?

A

A: Formation of a carbocation intermediate.

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2
Q

What happens to the carbocation in an Sₙ1 reaction?

A

A: A nucleophile attacks the carbocation, forming a substitution product.

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3
Q

What happens to the carbocation in an E1 reaction?

A

A: A base removes a β proton, forming a new π bond (elimination product).

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4
Q

What type of product is formed in an E1 reaction?

A

A: An alkene (elimination product).

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5
Q

Which step is rate-determining for both Sₙ1 and E1 reactions?

A

A: The formation of the carbocation intermediate.

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6
Q

In the Sₙ1 reaction, what role does the nucleophile play?

A

A: The nucleophile attacks the carbocation to form a stable product.

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7
Q

In the E1 reaction, what role does the base play?

A

A: The base abstracts a β proton, facilitating the formation of a double bond.

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8
Q

What is a key difference between Sₙ1 and E1 reactions?

A

A: Sₙ1 involves substitution, while E1 involves elimination.

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9
Q

Do Sₙ1 and E1 reactions share the same intermediate?

A

A: Yes, both share the same carbocation intermediate.

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