The first part of this paper contained the results of the examination of those hydrocarbons found in the distillate from the Torbane-hill mineral which were remarkable for their resistance to the action of monohydrated nitric and sulphuric acids. It was shown that, when in a state of purity, they possessed the composition, boiling-point, and density in the fluid and gaseous states, of the radicals of the ethylic class of alcohols. The present communication enters on the study of a group of substances as distinguished by the mobility, as the former are by the fixity of their hydrogen atoms. The examination of them has involved more labour than was experienced with their companion hydrocarbons; and the quantities obtained being necessarily small, even when working on a considerable scale, it has been impossible, at present, to do more than determine their constitution. The study of their combinations and decompositions is therefore necessarily deferred. Up to the present time we have been unacquainted with methods for the proximate analysis of complex mixtures such as that under study. It was necessary, therefore, to devise some plan for the purpose. The presence of benzole and its homologues was almost a matter of certainty, as they appear to be formed in all processes where coaly or bituminous matters are subjected to destructive distillation. In order to separate the hydrocarbons, the following method was adopted. Four ounces of bromine being placed in a large and well-stoppered flask, about eight volumes of water were added. The naphtha boiling in the fourteenth rectification between 71° and 77° Centigrade, was then added in very small portions, the whole being violently agitated after each addition. As the bromine, from its superior density, lay at the bottom of the water and the naphtha at the top, it will be seen that combination could not take place until the flask was shaken, at which time they united with a sharp hissing sound and a rise of temperature. The entire quantity of naphtha was absorbed by the bromine, forming a dense oil, becoming paler and at last colourless as the hydrocarbon increased in quantity. To ensure a definite product more bromine was used, so as to obtain a red oil, the excess being afterwards removed by agitation with mercury. During the process some substance is generated, acting powerfully on the eyes and causing a flow of tears; it is always present in the brominated oil, even when every trace of free bromine is removed. If the brominated oil be kept for some time in contact with water, it will be found that a third layer will make its appearance beneath the oil; this will be described hereafter.