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
Question
Book Icon
Chapter 7, Problem 7.22P
Interpretation Introduction

(a)

Interpretation:

The product of the reaction between phenol (C6H5OH) and the given compound is to be predicted.

Concept introduction:

In organometallic compounds, the metal-carbon bond is ionic. In most cases, the metal ion behaves as a spectator ion, and therefore, the organic part of the compound can be treated as a base or as an anionic nucleophile.

Whether the anion behaves as a base or a nucleophile depends on the whether the substrate contains an acidic proton or an easily approachable electron-poor carbon atom. The size of the anionic species is also a factor.

Interpretation Introduction

(b)

Interpretation:

The product of the reaction between phenol (C6H5OH) and the given compound is to be predicted.

Concept introduction:

In organometallic compounds, the metal-carbon bond is ionic. In most cases, the metal ion behaves as a spectator ion, and therefore, the organic part of the compound can be treated as a base or as an anionic nucleophile.

Whether the anion behaves as a base or a nucleophile depends on the whether the substrate contains an acidic proton or an easily approachable electron-poor carbon atom. The size of the anionic species is also a factor.

Interpretation Introduction

(c)

Interpretation:

The product of the reaction between phenol (C6H5OH) and the given compound is to be predicted.

Concept introduction:

In organometallic compounds, the metal-carbon bond is ionic. In most cases, the metal ion behaves as a spectator ion, and therefore, the organic part of the compound can be treated as a base or as an anionic nucleophile.

Whether the anion behaves as a base or a nucleophile depends on the whether the substrate contains an acidic proton or an easily approachable electron-poor carbon atom. The size of the anionic species is also a factor.

Interpretation Introduction

(d)

Interpretation:

The product of the reaction between phenol (C6H5OH) and the given compound is to be predicted.

Concept introduction:

In organometallic compounds, the metal-carbon bond is ionic. In most cases, the metal ion behaves as a spectator ion, and therefore, the organic part of the compound can be treated as a base or as an anionic nucleophile.

Whether the anion behaves as a base or a nucleophile depends on the whether the substrate contains an acidic proton or an easily approachable electron-poor carbon atom. The size of the anionic species is also a factor.

Blurred answer
Students have asked these similar questions
Predict the products of this organic reaction: + H ZH NaBH3CN H+ n. ? Click and drag to start drawing a structure. X
What is the missing reactant R in this organic reaction? + R H3O+ + • Draw the structure of R in the drawing area below. • Be sure to use wedge and dash bonds if it's necessary to draw one particular enantiomer. Click and drag to start drawing a structure.
What would be the best choices for the missing reagents 1 and 3 in this synthesis? 1 1. PPh3 2. n-BuLi 2 • Draw the missing reagents in the drawing area below. You can draw them in any arrangement you like. • Do not draw the missing reagent 2. If you draw 1 correctly, we'll know what it is. • Note: if one of your reagents needs to contain a halogen, use bromine. Click and drag to start drawing a structure.

Chapter 7 Solutions

Organic Chemistry: Principles and Mechanisms (Second Edition)

Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning