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 17, Problem 17.48P
Interpretation Introduction

(a)

Interpretation:

The mechanism of the given reaction is to be drawn and the major product is to be predicted.

Concept introduction:

Organometallic compounds have a polar covalent C-M bond. For example, the Grignard reagent (RMgX) has a polar C-Mg bond and an alkyl lithium reagent (RLi) has a polar covalent C-Li bond. Since carbon is bonded with an electropositive element, it possesses the partial negative charge and acts as the nucleophile as well as the base and can be treated as C- donor. Thus, it is used to form a new C-C bond with electrophilic carbon. The nucleophilic part (R-) of the organometallic reagent shows a nucleophilic addition reaction with carbonyl compounds. An imine on treatment with the organometallic reagent, Grignard reagent (RMgX) or an alkyl lithium reagent (RLi) followed by the acidic workup yields an amine.

Interpretation Introduction

(b)

Interpretation:

The mechanism of the specified reaction is to be drawn and the major product is to be predicted.

Concept introduction:

Organometallic compounds have a polar covalent C-M bond. For example, the Grignard reagent (RMgX) has a polar C-Mg bond and an alkyl lithium reagent (RLi) has a polar covalent C-Li bond. Since carbon is bonded with an electropositive element, it possesses the partial negative charge and acts as the nucleophile as well as the base and can be treated as C- donor. Thus it is used to form a new C-C bond with an electrophilic carbon. The nucleophilic part (R-) of the organometallic reagent shows a nucleophilic addition reaction with carbonyl compounds. An imine on treatment with the organometallic reagent, Grignard reagent (RMgX) or an alkyl lithium reagent (RLi) followed by the acidic workup yields an amine.

Interpretation Introduction

(c)

Interpretation:

The mechanism of the specified reaction is to be drawn and the major product is to be predicted.

Concept introduction:

Organometallic compounds have a polar covalent C-M bond. For example, the Grignard reagent (RMgX) has a polar C-Mg bond and an alkyl lithium reagent (RLi) has a polar covalent C-Li bond. Since carbon is bonded with an electropositive element, it possesses the partial negative charge and acts as the nucleophile as well as the base and can be treated as C- donor. Thus it is used to form a new C-C bond with an electrophilic carbon. The nucleophilic part (R-) of the organometallic reagent shows a nucleophilic addition reaction with carbonyl compounds. An imine on treatment with the organometallic reagent, Grignard reagent (RMgX) or an alkyl lithium reagent (RLi) followed by the acidic workup yields an amine.

Blurred answer
Students have asked these similar questions
Draw a detailed mechanism for the following reaction and include the major product
Predict the major product and mechanism
determine the major product and draw its mechanism.

Chapter 17 Solutions

Organic Chemistry: Principles and Mechanisms (Second Edition)

Ch. 17 - Prob. 17.11PCh. 17 - Prob. 17.12PCh. 17 - Prob. 17.13PCh. 17 - Prob. 17.14PCh. 17 - Prob. 17.15PCh. 17 - Prob. 17.16PCh. 17 - Prob. 17.17PCh. 17 - Prob. 17.18PCh. 17 - Prob. 17.19PCh. 17 - Prob. 17.20PCh. 17 - Prob. 17.21PCh. 17 - Prob. 17.22PCh. 17 - Prob. 17.23PCh. 17 - Prob. 17.24PCh. 17 - Prob. 17.25PCh. 17 - Prob. 17.26PCh. 17 - Prob. 17.27PCh. 17 - Prob. 17.28PCh. 17 - Prob. 17.29PCh. 17 - Prob. 17.30PCh. 17 - Prob. 17.31PCh. 17 - Prob. 17.32PCh. 17 - Prob. 17.33PCh. 17 - Prob. 17.34PCh. 17 - Prob. 17.35PCh. 17 - Prob. 17.36PCh. 17 - Prob. 17.37PCh. 17 - Prob. 17.38PCh. 17 - Prob. 17.39PCh. 17 - Prob. 17.40PCh. 17 - Prob. 17.41PCh. 17 - Prob. 17.42PCh. 17 - Prob. 17.43PCh. 17 - Prob. 17.44PCh. 17 - Prob. 17.45PCh. 17 - Prob. 17.46PCh. 17 - Prob. 17.47PCh. 17 - Prob. 17.48PCh. 17 - Prob. 17.49PCh. 17 - Prob. 17.50PCh. 17 - Prob. 17.51PCh. 17 - Prob. 17.52PCh. 17 - Prob. 17.53PCh. 17 - Prob. 17.54PCh. 17 - Prob. 17.55PCh. 17 - Prob. 17.56PCh. 17 - Prob. 17.57PCh. 17 - Prob. 17.58PCh. 17 - Prob. 17.59PCh. 17 - Prob. 17.60PCh. 17 - Prob. 17.61PCh. 17 - Prob. 17.62PCh. 17 - Prob. 17.63PCh. 17 - Prob. 17.64PCh. 17 - Prob. 17.65PCh. 17 - Prob. 17.66PCh. 17 - Prob. 17.67PCh. 17 - Prob. 17.68PCh. 17 - Prob. 17.69PCh. 17 - Prob. 17.70PCh. 17 - Prob. 17.71PCh. 17 - Prob. 17.72PCh. 17 - Prob. 17.73PCh. 17 - Prob. 17.74PCh. 17 - Prob. 17.75PCh. 17 - Prob. 17.76PCh. 17 - Prob. 17.77PCh. 17 - Prob. 17.78PCh. 17 - Prob. 17.79PCh. 17 - Prob. 17.80PCh. 17 - Prob. 17.81PCh. 17 - Prob. 17.82PCh. 17 - Prob. 17.83PCh. 17 - Prob. 17.84PCh. 17 - Prob. 17.1YTCh. 17 - Prob. 17.2YTCh. 17 - Prob. 17.3YTCh. 17 - Prob. 17.4YTCh. 17 - Prob. 17.5YTCh. 17 - Prob. 17.6YTCh. 17 - Prob. 17.7YTCh. 17 - Prob. 17.8YTCh. 17 - Prob. 17.9YTCh. 17 - Prob. 17.10YTCh. 17 - Prob. 17.11YTCh. 17 - Prob. 17.12YTCh. 17 - Prob. 17.13YTCh. 17 - Prob. 17.14YT
Knowledge Booster
Background pattern image
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY