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ChemInform Abstract: AROMATIC NUCLEOPHILIC SUBSTITUTION IN NUCLEOPHILIC SURFACTANTS. COMPARISON WITH ALKOXIDE REACTIONS

Clifford A. Bunton, Simon Diaz

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Abstract

Abstract Die Dinitrohalogenbenzole (I) reagieren mit den Alkanolationen (II) zu den intermediären Äthern (III), die mit Hydroxylionen zum Phenolat (IV) umgesetzt werden.

About this research paper

What this paper is about

Abstract Die Dinitrohalogenbenzole (I) reagieren mit den Alkanolationen (II) zu den intermediären Äthern (III), die mit Hydroxylionen zum Phenolat (IV) umgesetzt werden.

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Available abstract

Abstract Die Dinitrohalogenbenzole (I) reagieren mit den Alkanolationen (II) zu den intermediären Äthern (III), die mit Hydroxylionen zum Phenolat (IV) umgesetzt werden.

Key concepts: Alkoxide, Nucleophilic substitution, Nucleophilic aromatic substitution, Substitution reaction, Nucleophile, Chemistry, Radical-nucleophilic aromatic substitution, SNi

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ChemInform Abstract: AROMATIC NUCLEOPHILIC SUBSTITUTION IN NUCLEOPHILIC SURFACTANTS. COMPARISON WITH ALKOXIDE REACTIONS — Research Paper | ScholarLens