electronic ure must be planar or nearly planar so that overlap of these port must be cyclic with conjugated pi bonds ation of the pi electrons over the ring must decrease the electronic

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter5: Alkenes: Bonding, Nomenclature, And Properties
Section: Chapter Questions
Problem 5.11P: The structure of 1,2-propadiene (allene) is shown to the right. (a) Predict all approximate bond...
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Select the criteria for any compound to be considered antiaromatic.
Each atom in the ring must have an unhybridized p orbital
GOGO
Delocalization of the pi electrons over the ring must increase the electronic energy.
The structure must be planar or nearly planar so that overlap of these p orbitals is effective.
Structure must be cyclic with conjugated pi bonds.
Delocalization of the pi electrons over the ring must decrease the electronic energy.
The TT network must contain 4n+ 2 electrons (where n is the number of pi orbitals).
The TT network must contain 4n+ 2 electrons (where n is a whole number).
Transcribed Image Text:Select the criteria for any compound to be considered antiaromatic. Each atom in the ring must have an unhybridized p orbital GOGO Delocalization of the pi electrons over the ring must increase the electronic energy. The structure must be planar or nearly planar so that overlap of these p orbitals is effective. Structure must be cyclic with conjugated pi bonds. Delocalization of the pi electrons over the ring must decrease the electronic energy. The TT network must contain 4n+ 2 electrons (where n is the number of pi orbitals). The TT network must contain 4n+ 2 electrons (where n is a whole number).
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