Issue 1, 2003
From the journal:

Organic & Biomolecular Chemistry

Non-steady-state kinetic study of the SN2 reaction between p-nitrophenoxide ion and methyl iodide in aprotic solvents containing water. Evidence for a 2-step mechanism

Yun Lu,a   Kishan L. Handooa  and  Vernon D. Parker*a  

* Corresponding authors

a Department of Chemistry and Biochemistry, Utah State University, Logan, Utah, USA

Abstract

Non-steady-state kinetic studies reveal that the SN2 reaction between p-nitrophenoxide ion and methyl iodide in acetonitrile containing water follows a 2-step mechanism involving the formation of a kinetically significant intermediate.

Graphical abstract: Non-steady-state kinetic study of the SN2 reaction between p-nitrophenoxide ion and methyl iodide in aprotic solvents containing water. Evidence for a 2-step mechanism

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Article information

DOI
https://doi.org/10.1039/B208635B
Article type
Communication
Submitted
05 Sep 2002
Accepted
07 Oct 2002
First published
08 Nov 2002

Org. Biomol. Chem., 2003,1, 36-38

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Non-steady-state kinetic study of the SN2 reaction between p-nitrophenoxide ion and methyl iodide in aprotic solvents containing water. Evidence for a 2-step mechanism

Y. Lu, K. L. Handoo and V. D. Parker, Org. Biomol. Chem., 2003, 1, 36 DOI: 10.1039/B208635B

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