Note 1 — Chapter X · SODIUM CHLORIDE—BERTHOLLET'S LAWS—HYDROCHLORIC ACID
George Kamensky translation
But it is impossible to foretell all the compounds formed by an element from its atomicity or valency, because the atomicity of the elements is variable, and furthermore this variability is not identical for different elements. In CO2, COX2, CH4, and the multitude of carbon compounds corresponding with them, the C is quadrivalent, but in CO either the carbon must be taken as bivalent or the atomicity of oxygen be accounted as variable. Moreover, carbon is an example of an element which preserves its atomicity to a greater degree than most of the other elements. Nitrogen in NH3, NH2(OH), N2O3, and even in CNH, must be considered as trivalent, but in NH4Cl, NO2(OH), and in all their corresponding compounds it is necessarily pentavalent. In N2O, if the atomicity of oxygen = 2, nitrogen has an uneven atomicity (1, 3, 5), whilst in NO it is bivalent. If sulphur be bivalent, like oxygen, in many of its compounds (for example, H2S, SCl2, KHS, &c.), then it could not be foreseen from this that it would form SO2, SO3, SCl4, SOCl2, and a series of similar compounds in which its atomicity must be acknowledged as greater than 2. Thus SO2, sulphurous anhydride, has many points in common with CO2, and if carbon be quadrivalent then the S in SO2 is quadrivalent. Therefore the principle of atomicity (valency) of the elements cannot be considered established as the basis for the study of the elements, although it gives an easy method of grasping many analogies. I consider the four following as the chief obstacles to acknowledging the atomicity of the elements as a primary conception for the consideration of the properties of the elements: 1. Such univalent elements as H, Cl, &c., appear in a free state as molecules H2, Cl2, &c., and are consequently like the univalent radicles CH3, OH, CO2H, &c., which, as might be expected, appear as C2H6, O2H2, C2O4H2 (ethane, hydrogen peroxide, oxalic acid), whilst on the other hand, potassium and sodium (perhaps also iodine at a high temperature) contain only one atom, K, Na, in the molecule in a free state. Hence it follows that free affinities may exist. Granting this, nothing prevents the assumption that free affinities exist in all unsaturated compounds; for example, two free affinities in NH3. If such instances of free affinities be admitted, then all the possible advantages to be gained by the application of the doctrine of atomicity (valency) are lost. 2. There are instances—for example, Na2H—where univalent elements are combined in molecules which are more complex than R2, and form molecules, R3, R4, &c.; this may again be either taken as evidence of the existence of free affinities, or else necessitates such primary univalent elements as sodium and hydrogen being considered as variable in their atomicity. 3. The periodic system of the elements, with which we shall afterwards become acquainted, shows that there is a law or rule for the variation of the forms of oxygen and hydrogen compounds; chlorine is univalent with respect to hydrogen, and septavalent with respect to oxygen; sulphur is bivalent to hydrogen, and sexavalent to oxygen; phosphorus is trivalent to hydrogen and pentavalent in respect to oxygen—the sum is in every case equal to 8. Only carbon and its analogues (for example, silicon) are quadrivalent to both hydrogen and oxygen. Hence the power of the elements to change their atomicity is an essential part of their nature, and therefore constant valency cannot he considered as a fundamental property. 4. Crystallo-hydrates (for instance, NaCl,2H2O, or NaBr,2H2O), double salts (such as PtCl4,2KCl,H2SiF6, &c.), and similar complex compounds (and, according to Chap. I., solutions also) demonstrate the capacity not only of the elements themselves, but also of their saturated and limiting compounds, of entering into further combination. Therefore the admission of a definite limited atomicity of the elements includes in itself an admission of limitation which is not in accordance with the nature of chemical reactions.