Organic Chemistry: Principles and Mechanisms (Second Edition)
Organic Chemistry: Principles and Mechanisms (Second Edition)
2nd Edition
ISBN: 9780393663556
Author: Joel Karty
Publisher: W. W. Norton & Company
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Chapter 14, Problem 14.23P
Interpretation Introduction

Interpretation:

Assuming the given compound is planar, it is to be determined and explained whether it is aromatic, antiaromatic, or nonaromatic.

Concept introduction:

Electrons can be resonance delocalized over a set of atoms that contribute conjugated p-orbitals to a single π system of molecular orbitals. For an acyclic conjugated system, the π electrons are the ones that can be shifted via resonance from one end to the other. Counting of the π systems and number of electrons is useful when a compound contains a triple bond. According to the MO theory, the two pi bonds are perpendicular to each other in a triple bond. Therefore, only one of those pi bonds can be conjugated with the neighboring π system.

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Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Select to Edit Arrows H H Select to Add Arrows > H CFCI: Select to Edit Arrows H Select to Edit Arrows
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Chapter 14 Solutions

Organic Chemistry: Principles and Mechanisms (Second Edition)

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