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The third step displays the carboxylate functionality leaving since it is the best leaving group. As a result the resulting carboxylate attacks an alpha hydrogen to create the enol functionality again in step four.

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George Simms Hammond (May 22, 1921 – October 5, 2005) was an American scientist and theoretical chemist who developed "Hammond's postulate", and fathered organic photochemistry,–the general theory of the geometric structure of the…

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2-Nitroaniline is an organic compound with the formula H2NC6H4NO2. It is a derivative of aniline, carrying a nitro functional group in position 2. It is mainly used as a precursor to o-phenylenediamine.

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as well as new advances in well-known areas of Organic chemistry. 94For an account of the early history of Aromaticity, see Snyder, J.P., in Snyder, J.P. 

^ Graham, Solomons, T. W. Organic chemistry. Fryhle, Craig B.,, Snyder, S. A. (Scott A.) (11e ed.). Hoboken, NJ. p. 869. ISBN 9781118133576. OCLC 820665397. The third step displays the carboxylate functionality leaving since it is the best leaving group. As a result the resulting carboxylate attacks an alpha hydrogen to create the enol functionality again in step four. It was developed in 1926 by American engineer Murray Raney for the hydrogenation of vegetable oils. 2-Nitroaniline is an organic compound with the formula H2NC6H4NO2. It is a derivative of aniline, carrying a nitro functional group in position 2. It is mainly used as a precursor to o-phenylenediamine. George Simms Hammond (May 22, 1921 – October 5, 2005) was an American scientist and theoretical chemist who developed "Hammond's postulate", and fathered organic photochemistry,–the general theory of the geometric structure of the…