b. antibonding antibonding MOs Aromatic compounds are stable because they have bonding MOs filled bonding molecular MOS bonding MOs orbitals. A Figure 8.17 The distribution of electrons in the molecular orbitals of (a) benzene and (b) the cyclopentadienyl anion. Energy Energy

Principles of Modern Chemistry
8th Edition
ISBN:9781305079113
Author:David W. Oxtoby, H. Pat Gillis, Laurie J. Butler
Publisher:David W. Oxtoby, H. Pat Gillis, Laurie J. Butler
Chapter6: Quantum Mechanics And Molecular Structure
Section: Chapter Questions
Problem 5P: Compare the electron density in the 1g and 1u* molecular orbitals for H2+ shown in Figure 6.5 with...
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Following the instructions for drawing the energy levels of the molecular orbitals for the compounds shown in Figure 8.17, draw the energy levels of the molecular orbitals for the cycloheptatrienyl cation, the cycloheptatrienyl anion, and the cyclopropenyl cation. For each compound, show the distribution of the p electrons. Which of the compounds are aromatic?

b.
antibonding
antibonding
MOs
Aromatic compounds are
stable because they have
bonding MOs filled bonding molecular
MOS
bonding MOs
orbitals.
A Figure 8.17
The distribution of electrons in the molecular orbitals of (a) benzene and (b) the cyclopentadienyl anion.
Energy
Energy
Transcribed Image Text:b. antibonding antibonding MOs Aromatic compounds are stable because they have bonding MOs filled bonding molecular MOS bonding MOs orbitals. A Figure 8.17 The distribution of electrons in the molecular orbitals of (a) benzene and (b) the cyclopentadienyl anion. Energy Energy
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