Mechanisms: electrophilic addition Flashcards

1
Q

What group forms what group in this reaction?

A

Alkenes form alkanes

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2
Q

What is the general equation?

A

Alkene + reagent —> 1 product

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3
Q

What happens to the double bond in the alkene?

A

It becomes a single bond. An electrophile is often needed to break the double C bond

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4
Q

What are carbocations?

A

A positive charge on carbon atom

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5
Q

What is a primary carbocation?

A

Where there is 1 other carbon atom attached to carbocation

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6
Q

What is a secondary carbocation?

A

Where there is 2 other carbon atoms attached to carbocation

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7
Q

What is a tertiary carbocation?

A

Where there is 3 other carbon atoms attached to carbocation

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8
Q

What do R1, R2 and R3 stand for on the structure of carbocations?

A

Alkyl groups such as methyl and ethyl. They can all be the same or different

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9
Q

What is Markownikoff’s rule?

A
  • Methyl and ethyl groups have an electron releasing effect relative to H atom
  • The more stable the carbocation, the longer the time is remains in the reaction mixture
  • Which means it has a greater chance of reacting with an anion to form a product
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10
Q

What do more stable carbocations form?

A

Major products

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11
Q

What do less stable carbocations form?

A

Minor products

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12
Q

What do electrophilic addition reactions go via?

A

An intermediate carbocation

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13
Q

Which type of carbocation is most stable and which is least stable?

A

A tertiary carbocation is most stable so it becomes major product relative to others
A primary carbocation is least stable so becomes minor product

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