The mechanism of substitution reactions in the aromatic nucleus. Part IV

…, JW Cook, MA Matthews

Index: Barnett; Cook; Matthews Recueil des Travaux Chimiques des Pays-Bas, 1925 , vol. 44, p. 823

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Abstract

It has already been shown') that in many of their reactions the anthracene dihalides and their Bt.-substitution products show a considerable tendency to undergo change in geometrical configuration, and that in the trans-isomers the tendency for re-establishment of the “bridge” to take place is considerably greater than in the corresponding cis-isomers. Of those compounds which have been studied up to the present 1: 5dichloroanthracene has ...