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: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter18: Aromaticity
Section: Chapter Questions
Problem 26CTQ
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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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