Chapter 16 & 17 Discussion

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Chapter 16 & 17 Discussion

description

Chapter 16 & 17 Discussion. Meso = identical. Endo and exo are meaningless without substitutents to provide frame of reference. diene. dienophile. Recognize that this is a Diels Alder reaction by the diene and dienophile (on the right). 2) Draw a cyclohexene ring. - PowerPoint PPT Presentation

Transcript of Chapter 16 & 17 Discussion

Page 1: Chapter  16 & 17  Discussion

Chapter 16 & 17 Discussion

Page 2: Chapter  16 & 17  Discussion

Endo and exo are meaningless without substitutents to provide frame of reference

Meso = identical

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1) Recognize that this is a Diels Alder reaction by the diene and dienophile (on the right)

2) Draw a cyclohexene ring

3) Build models of the possible isomers that could result from the cycloaddition

4) Use resonance to help predict regioisomer

5) Temperature for endo/exo preference.

diene dienophile

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3) Build models of the possible isomers that could result from the cycloaddition4) Use resonance to help predict regioisomer

5) Temperature for endo/exo preference.

endo

exo

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Endo and exo

+ enantiomer + enantiomer

Exo (thermodynamic product)

Endo (kinetic product)

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?

1) Recognize that this is a Diels Alder reaction by the diene and dienophile (on the right)

2) Draw a cyclohexene ring

3) Build models of the possible isomers that could result from the cycloaddition

4) Use resonance to help predict regioisomer

5) Temperature for endo/exo preference.

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Four possible regioisomers and diastereomers (+ enantiomers)

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Resonance contributors show which regioisomers will form

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Regiochemistry is established. How about endo or exo?

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?

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No meta.

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Problem:Diels-Alder Reactants?

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Flat, cyclic, conjugated pi system and 4n + 2 pi electrons

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Aromatic if 2, 6, 10, 14, 18 pi electrons…..Anti-aromatic if 4, 8, 12, 16, ….. pi electrons

If neither then not aromatic or anti-aromatic.

Anti-aromatic more stable than expected.

Anti-aromatic – less stable and likely will not form at all.

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4 pi electrons. Antiaromatic

Cyclopropenyl anion

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Aromatic?

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6 pi electrons, aromatic

Cyclopentadienyl anion

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Aromatic?

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10 pi electrons aromatic

Lactarius azulene

chamomileYarrow

Azulene

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aromatic : cyclic, 10 electrons, flat, conjugated

Naphthalene

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Why is naphthalene nonpolar and azulene polar?

Azulenenaphthalene

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Aromatic, anti-aromatic or neither?

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Aromatic, anti-aromatic or neither?

Depends on conformation. If flat and fully conjugated, antiaromatic!!!!

Lower energy conformation (than anti-aromatic) is not flat

8 pi electrons