ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE
ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE
2nd Edition
ISBN: 9780393666144
Author: KARTY
Publisher: NORTON
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Chapter 14, Problem 14.7YT
Interpretation Introduction

Interpretation:

It is to be shown how many nodal planes are perpendicular to the bonding axes in π6* MO of benzene from the given figure.

Concept introduction:

The MO arises from interacting p AOs of two atoms. MO energies differ as a result of constructive and destructive interference among contributing AOs. Each pair of overlapping AOs with the same phase lowers the MO energy and corresponds to a bonding interaction in an MO while each pair of overlapping AOs with the opposite phases raises the MO energy and corresponds to an antibonding interaction in an MO. The destructive interference gives rise to a nodal plane. The contributions of the AOs to produce a bonding, nonbonding or antibonding MO depend on the net interaction.  In the MO diagram, only π electrons are considered. In the case of a conjugated system, the number of π electrons corresponds to p orbitals, which are considered atomic orbitals (AOs) in the MO diagram. For conjugated alkene, there are also equal numbers of bonding and antibonding orbitals. The bonding interaction results from adjacent p orbitals, which are in the same phase, and when the adjacent orbital in the opposite phase results in antibonding interaction, which is also represented by a nodal plane.

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I have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."
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Chapter 14 Solutions

ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE

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