Retrosynthesis: When No2 bond breaks, which one would be the next better leaving group, SO3H or cyclopentane?    Why is SO3H a better leaving group than cyclopentane?   Why NO2 is the first one that leave in Retrosynthesis, what make NO2 a better leaving group over SO3H or cyclopentane?

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Retrosynthesis: When No2 bond breaks, which one would be the next better leaving group, SO3H or cyclopentane? 

 

Why is SO3H a better leaving group than cyclopentane?

 

Why NO2 is the first one that leave in Retrosynthesis, what make NO2 a better leaving group over SO3H or cyclopentane?

The image depicts a chemical structure with the following components:

- A benzene ring, which is a hexagonal arrangement of carbon atoms with alternating double bonds.
- Attached to the benzene ring, there is a nitro group (NO₂) and a sulfonic acid group (SO₃H).
- A cyclopentane ring is connected to the benzene ring. It is a five-membered carbon ring with single bonds.

This structure could represent a substituted aromatic compound with specific functional groups influencing its chemical properties and reactivity.
Transcribed Image Text:The image depicts a chemical structure with the following components: - A benzene ring, which is a hexagonal arrangement of carbon atoms with alternating double bonds. - Attached to the benzene ring, there is a nitro group (NO₂) and a sulfonic acid group (SO₃H). - A cyclopentane ring is connected to the benzene ring. It is a five-membered carbon ring with single bonds. This structure could represent a substituted aromatic compound with specific functional groups influencing its chemical properties and reactivity.
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