BEHAVIOUR OF SOME ISOLATED AND CONJUGATED UNSATURATED COMPOUNDS, ARENES AND AROMATIC HETEROCYCLES IN A Ni-Al/NaOH REDUCING SYSTEM

  • Mirela Suceveanu
    „Vasile Alecsandri” University of Bacau, Faculty of Engineering, Department of Food and Chemical Engineering, Calea Marasesti 157, 600115 Bacau, Romania
    mirela.suceveanu@ub.ro
  • Matei Raicopol
    „Politehnica” University of Bucharest, Faculty of Applied Chemistry and Materials Science, Department of Organic Chemistry „Costin Nenitzescu", Gh. Polizu 1-7, 011061 Bucharest, Romania
  • Adriana Fînaru
    „Vasile Alecsandri” University of Bacau, Faculty of Engineering, Department of Food and Chemical Engineering, Calea Marasesti 157, 600115 Bacau, Romania
  • Sorin I. Roşca
    „Politehnica” University of Bucharest, Faculty of Applied Chemistry and Materials Science, Department of Organic Chemistry „Costin Nenitzescu", Gh. Polizu 1-7, 011061 Bucharest, Romania

Abstract

In this paper we present the results of some experiments in which substrates representing various unsaturated and aromatic systems were tested in reduction reactions with Ni-Al alloy in aqueous NaOH and we highlight the relationships between the structure and the reactivity of the investigated compounds. We have found that unsaturated compounds containing isolated double bonds carbon-carbon and polynuclear condensed ring aromatics present an advanced inertness to the reduction process by the aluminum component of the Ni-Al/NaOH system. Unlike them, unsaturated compounds with C=C conjugated bonds are very reactive to the Ni-Al/NaOH system, 1,4 reduction processes being facilitated, behaviour attributed to the polar nature of the conjugated systems. The heterocyclic compounds have a higher reactivity than their homologues carbocyclic compounds.

Cuvinte cheie

aromatic compounds GC-MS Ni-Al alloy reduction reaction unsaturated compounds