Alkenes and Peracids Flashcards

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1
Q

What is a peracid?

A

R-COOOH
C=O
C-O
O-OH

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2
Q

What product is formed when you react an alkene with a peracid?

A

epoxide

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3
Q

Where on a peracid is the nucleophile likely to attack and why?

A

The oxygen on the OH

The O-O bond is very weak and it breaks the weakest bond

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4
Q

What is the most commonly used peracid? Draw its structure.

A

mCPBA

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5
Q

What is a negative about mCPBA?

A

It is very reactive and explosive at high amounts/concentrations
All products are organic, hard to seperate byproduct from the desired product

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6
Q

How many mechanistic steps does the formation of the peracid using mCPBA occur in?

A

1

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7
Q

What type of reaction is peracid formation?

A

Synaddition

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8
Q

What happens during a peracid formation reaction?

A

The charge is delocalised to make it more stable

Both c-o bonds are formed at the same time

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9
Q

If the alkene is cis, what will the epoxide be?

A

Cis

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10
Q

If the alkene is trans, what will the epoxide be?

A

Trans

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11
Q

How is the formation of epoxides stereospecific?

A

Each diastereomer of an alkene gives a different diastereomer of the epoxide product

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12
Q

What type of reaction do epoxides go to open the ring?

A

Sn2 reaction with nucleophiles

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13
Q

Overall, what does the epoxide ring opening result in?

A

Anti-addition of OH and the nucleophile

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14
Q

Can epoxides ring open by both SN1 and SN2? Draw the mechanism

A

Yes

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15
Q

What type of reaction will the alkene undergo if it is unsymmetrical?

A

SN2

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16
Q

Where will the nucleophile attack in the SN2 reaction?

A

The least hindered end of the epoxide

17
Q

What happens when epoxides react with nucleophiles in SN1 conditions?

A

The nucleophile will add to whichever end of the epoxide is best able to stabilise a positive charge

18
Q

What conditions are needed for SN1?

A

Acid catalyst