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Issue 0, 1968
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The kinetics and mechanism of the electrophilic substitution of heteroaromatic compounds. Part XIII. The mononitration of 2-phenylpyridine and its N-oxide

Abstract

A kinetic study of the nitration of 2-phenylpyridine and its N-oxide shows that both compounds react as their conjugate acids. Partial rate factors are calculated for reaction at the 2′-, 3′-, and 4′-positions and compared with literature data.

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J. Chem. Soc. B, 1968, 862-864
Article type
Paper

The kinetics and mechanism of the electrophilic substitution of heteroaromatic compounds. Part XIII. The mononitration of 2-phenylpyridine and its N-oxide

A. R. Katritzky and M. Kingsland, J. Chem. Soc. B, 1968, 862
DOI: 10.1039/J29680000862

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