EBK GET READY FOR ORGANIC CHEMISTRY
EBK GET READY FOR ORGANIC CHEMISTRY
2nd Edition
ISBN: 8220100576379
Author: KARTY
Publisher: PEARSON
Question
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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.

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Chapter 17 Solutions

EBK GET READY FOR ORGANIC CHEMISTRY

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
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