Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
2nd Edition
ISBN: 9780393655551
Author: KARTY, Joel
Publisher: W. W. Norton & Company
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Chapter G, Problem G.8YT
Interpretation Introduction

Interpretation:

The McLafferty rearrangement for the molecular ion of pentanoic acid is to be drawn.

Concept introduction:

These two fragmentation pathways – heterolysis and α-cleavage – are also common to other compound classes that have functional groups with heteroatoms, such as amines, ethers, and alcohols. Depending on the identity of the functional group as well as the specific structure of the compound, one of these fragmentation pathways can be highly favored over the other.

In addition to α-cleavage, there is another fragmentation pathway characteristic of carbonyl-containing compounds. A carbonyl-containing compound can undergo a McLafferty rearrangement if an alkyl group attached to the carbonyl carbon possesses a γ-carbon with at least one hydrogen atom.

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#1. Retro-Electrochemical Reaction: A ring has been made, but the light is causing the molecule to un- cyclize. Undo the ring into all possible molecules. (2pts, no partial credit) hv
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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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