ORGANIC CHEM +SG +SAPLING >IP<
ORGANIC CHEM +SG +SAPLING >IP<
6th Edition
ISBN: 9781319171179
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 19, Problem 19.20P
Interpretation Introduction

Interpretation:

The compound among A, B, and C that could not be synthesized by a hydride reduction of an aldehyde or ketone is to be identified.

Concept introduction:

The metal hydride reagents are good reducing agents such as LiAlH4 and NaBH4. The aldehyde and ketone are carbonyl compounds. Aldehyde and ketone are reduced to form primary and secondary alcohol. The tertiary alcohol can also be produced by reduction of aldehyde or ketone.

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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 19 Solutions

ORGANIC CHEM +SG +SAPLING >IP<

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