To predict the product and mechanism of given reaction has to be identified. Concept Introduction: The assault can take place at also end of the triple bond with equivalent probability, explaining the experiential results. This proposed mechanism is called elimination-addition. A nucleophilic aromatic replacement is a replacement reaction in organic chemistry in which the nucleophile displaces a good departure group, such as a halide, on an aromatic ring. Present are nucleophilic replacement mechanisms encountered with perfumed systems. The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance. Benzyne is an unstable transitional, which has a structure parallel to benzene with an additional pi bond. The third pi bond is fashioned by the partly cover of sp 2 hybridized orbitals external the ring. While the molecule is stressed it is highly immediate species.

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Chapter 18, Problem 56PP

Interpretation Introduction

Interpretation:

To predict the product and mechanism of given reaction has to be identified.

Concept Introduction:

The assault can take place at also end of the triple bond with equivalent probability, explaining the experiential results. This proposed mechanism is called elimination-addition.

A nucleophilic aromatic replacement is a replacement reaction in organic chemistry in which the nucleophile displaces a good departure group, such as a halide, on an aromatic ring. Present are nucleophilic replacement mechanisms encountered with perfumed systems.

The delocalized nature of pi electrons in benzene attributes a special property to benzene called resonance.

Benzyne is an unstable transitional, which has a structure parallel to benzene with an additional pi bond. The third pi bond is fashioned by the partly cover of sp2 hybridized orbitals external the ring. While the molecule is stressed it is highly immediate species.

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