A History of Science Volume IV Part 2

Be that as it may, it is certain enough that Dalton's contemporaries were at first little impressed with the novel atomic theory. Just at this time, as it chanced, a dispute was waging in the field of chemistry regarding a matter of empirical fact which must necessarily be settled before such a theory as that of Dalton could even hope for a bearing.

This was the question whether or not chemical elements unite with one another always in definite proportions. Berthollet, the great co-worker with Lavoisier, and now the most authoritative of living chemists, contended that substances combine in almost indefinitely graded proportions between fixed extremes. He held that solution is really a form of chemical combination--a position which, if accepted, left no room for argument.

But this contention of the master was most actively disputed, in particular by Louis Joseph Proust, and all chemists of repute were obliged to take sides with one or the other. For a time the authority of Berthollet held out against the facts, but at last acc.u.mulated evidence told for Proust and his followers, and towards the close of the first decade of our century it came to be generally conceded that chemical elements combine with one another in fixed and definite proportions.

More than that. As the a.n.a.lysts were led to weigh carefully the quant.i.ties of combining elements, it was observed that the proportions are not only definite, but that they bear a very curious relation to one another. If element A combines with two different proportions of element B to form two compounds, it appears that the weight of the larger quant.i.ty of B is an exact multiple of that of the smaller quant.i.ty. This curious relation was noticed by Dr. Wollaston, one of the most accurate of observers, and a little later it was confirmed by Johan Jakob Berzelius, the great Swedish chemist, who was to be a dominating influence in the chemical world for a generation to come. But this combination of elements in numerical proportions was exactly what Dalton had noticed as early as 1802, and what bad led him directly to the atomic weights. So the confirmation of this essential point by chemists of such authority gave the strongest confirmation to the atomic theory.

During these same years the rising authority of the French chemical world, Joseph Louis Gay-Lussac, was conducting experiments with gases, which he had undertaken at first in conjunction with Humboldt, but which later on were conducted independently. In 1809, the next year after the publication of the first volume of Dalton's New System of Chemical Philosophy, Gay-Lussac published the results of his observations, and among other things brought out the remarkable fact that gases, under the same conditions as to temperature and pressure, combine always in definite numerical proportions as to volume. Exactly two volumes of hydrogen, for example, combine with one volume of oxygen to form water.

Moreover, the resulting compound gas always bears a simple relation to the combining volumes. In the case just cited, the union of two volumes of hydrogen and one of oxygen results in precisely two volumes of water vapor.

Naturally enough, the champions of the atomic theory seized upon these observations of Gay-Lussac as lending strong support to their hypothesis--all of them, that is, but the curiously self-reliant and self-sufficient author of the atomic theory himself, who declined to accept the observations of the French chemist as valid. Yet the observations of Gay-Lussac were correct, as countless chemists since then have demonstrated anew, and his theory of combination by volumes became one of the foundation-stones of the atomic theory, despite the opposition of the author of that theory.

The true explanation of Gay-Lussac's law of combination by volumes was thought out almost immediately by an Italian savant, Amadeo, Avogadro, and expressed in terms of the atomic theory. The fact must be, said Avogadro, that under similar physical conditions every form of gas contains exactly the same number of ultimate particles in a given volume. Each of these ultimate physical particles may be composed of two or more atoms (as in the case of water vapor), but such a compound atom conducts itself as if it were a simple and indivisible atom, as regards the amount of s.p.a.ce that separates it from its fellows under given conditions of pressure and temperature. The compound atom, composed of two or more elementary atoms, Avogadro proposed to distinguish, for purposes of convenience, by the name molecule. It is to the molecule, considered as the unit of physical structure, that Avogadro's law applies.

This vastly important distinction between atoms and molecules, implied in the law just expressed, was published in 1811. Four years later, the famous French physicist Ampere outlined a similar theory, and utilized the law in his mathematical calculations. And with that the law of Avogadro dropped out of sight for a full generation. Little suspecting that it was the very key to the inner mysteries of the atoms for which they were seeking, the chemists of the time cast it aside, and let it fade from the memory of their science.

This, however, was not strange, for of course the law of Avogadro is based on the atomic theory, and in 1811 the atomic theory was itself still being weighed in the balance. The law of multiple proportions found general acceptance as an empirical fact; but many of the leading lights of chemistry still looked askance at Dalton's explanation of this law. Thus Wollaston, though from the first he inclined to acceptance of the Daltonian view, cautiously suggested that it would be well to use the non-committal word "equivalent" instead of "atom"; and Davy, for a similar reason, in his book of 1812, speaks only of "proportions,"

binding himself to no theory as to what might be the nature of these proportions.

At least two great chemists of the time, however, adopted the atomic view with less reservation. One of these was Thomas Thomson, professor at Edinburgh, who, in 1807, had given an outline of Dalton's theory in a widely circulated book, which first brought the theory to the general attention of the chemical world. The other and even more noted advocate of the atomic theory was Johan Jakob Berzelius. This great Swedish chemist at once set to work to put the atomic theory to such tests as might be applied in the laboratory. He was an a.n.a.lyst of the utmost skill, and for years he devoted himself to the determination of the combining weights, "equivalents" or "proportions," of the different elements. These determinations, in so far as they were accurately made, were simple expressions of empirical facts, independent of any theory; but gradually it became more and more plain that these facts all harmonize with the atomic theory of Dalton. So by common consent the proportionate combining weights of the elements came to be known as atomic weights--the name Dalton had given them from the first--and the tangible conception of the chemical atom as a body of definite const.i.tution and weight gained steadily in favor.

From the outset the idea had had the utmost tangibility in the mind of Dalton. He had all along represented the different atoms by geometrical symbols--as a circle for oxygen, a circle enclosing a dot for hydrogen, and the like--and had represented compounds by placing these symbols of the elements in juxtaposition. Berzelius proposed to improve upon this method by subst.i.tuting for the geometrical symbol the initial of the Latin name of the element represented--O for oxygen, H for hydrogen, and so on--a numerical coefficient to follow the letter as an indication of the number of atoms present in any given compound. This simple system soon gained general acceptance, and with slight modifications it is still universally employed. Every school-boy now is aware that H2O is the chemical way of expressing the union of two atoms of hydrogen with one of oxygen to form a molecule of water. But such a formula would have had no meaning for the wisest chemist before the day of Berzelius.

The universal fame of the great Swedish authority served to give general currency to his symbols and atomic weights, and the new point of view thus developed led presently to two important discoveries which removed the last lingering doubts as to the validity of the atomic theory. In 1819 two French physicists, Dulong and Pet.i.t, while experimenting with heat, discovered that the specific heats of solids (that is to say, the amount of heat required to raise the temperature of a given ma.s.s to a given degree) vary inversely as their atomic weights. In the same year Eilhard Mitscherlich, a German investigator, observed that compounds having the same number of atoms to the molecule are disposed to form the same angles of crystallization--a property which he called isomorphism.

Here, then, were two utterly novel and independent sets of empirical facts which harmonize strangely with the supposition that substances are composed of chemical atoms of a determinate weight. This surely could not be coincidence--it tells of law. And so as soon as the claims of Dulong and Pet.i.t and of Mitscherlich had been substantiated by other observers, the laws of the specific heat of atoms, and of isomorphism, took their place as new levers of chemical science. With the aid of these new tools an impregnable breastwork of facts was soon piled about the atomic theory. And John Dalton, the author of that theory, plain, provincial Quaker, working on to the end in semi-retirement, became known to all the world and for all time as a master of masters.

HUMPHRY DAVY AND ELECTRO-CHEMISTRY

During those early years of the nineteenth century, when Dalton was grinding away at chemical fact and theory in his obscure Manchester laboratory, another Englishman held the attention of the chemical world with a series of the most brilliant and widely heralded researches. This was Humphry Davy, a young man who had conic to London in 1801, at the instance of Count Rumford, to a.s.sume the chair of chemical philosophy in the Royal Inst.i.tution, which the famous American had just founded.

Here, under Davy's direction, the largest voltaic battery yet constructed had been put in operation, and with its aid the brilliant young experimenter was expected almost to perform miracles. And indeed he scarcely disappointed the expectation, for with the aid of his battery he transformed so familiar a substance as common potash into a metal which was not only so light that it floated on water, but possessed the seemingly miraculous property of bursting into flames as soon as it came in contact with that fire-quenching liquid. If this were not a miracle, it had for the popular eye all the appearance of the miraculous.

What Davy really had done was to decompose the potash, which hitherto had been supposed to be elementary, liberating its oxygen, and thus isolating its metallic base, which he named pota.s.sium. The same thing was done with soda, and the closely similar metal sodium was discovered--metals of a unique type, possessed of a strange avidity for oxygen, and capable of seizing on it even when it is bound up in the molecules of water. Considered as mere curiosities, these discoveries were interesting, but aside from that they were of great theoretical importance, because they showed the compound nature of some familiar chemicals that had been regarded as elements. Several other elementary earths met the same fate when subjected to the electrical influence; the metals barium, calcium, and strontium being thus discovered. Thereafter Davy always referred to the supposed elementary substances (including oxygen, hydrogen, and the rest) as "unde-compounded" bodies. These resist all present efforts to decompose them, but how can one know what might not happen were they subjected to an influence, perhaps some day to be discovered, which exceeds the battery in power as the battery exceeds the blowpipe?

Another and even more important theoretical result that flowed from Davy's experiments during this first decade of the century was the proof that no elementary substances other than hydrogen and oxygen are produced when pure water is decomposed by the electric current. It was early noticed by Davy and others that when a strong current is pa.s.sed through water, alkalies appear at one pole of the battery and acids at the other, and this though the water used were absolutely pure. This seemingly told of the creation of elements--a trans.m.u.tation but one step removed from the creation of matter itself--under the influence of the new "force." It was one of Davy's greatest triumphs to prove, in the series of experiments recorded in his famous Bakerian lecture of 1806, that the alleged creation of elements did not take place, the substances found at the poles of the battery having been dissolved from the walls of the vessels in which the water experimented upon had been placed.

Thus the same implement which had served to give a certain philosophical warrant to the fading dreams of alchemy banished those dreams peremptorily from the domain of present science.

"As early as 1800," writes Davy, "I had found that when separate portions of distilled water, filling two gla.s.s tubes, connected by moist bladders, or any moist animal or vegetable substances, were submitted to the electrical action of the pile of Volta by means of gold wires, a nitro-muriatic solution of gold appeared in the tube containing the positive wire, or the wire transmitting the electricity, and a solution of soda in the opposite tube; but I soon ascertained that the muriatic acid owed its existence to the animal or vegetable matters employed; for when the same fibres of cotton were made use of in successive experiments, and washed after every process in a weak solution of nitric acid, the water in the apparatus containing them, though acted on for a great length of time with a very strong power, at last produced no effects upon nitrate of silver.

"In cases when I had procured much soda, the gla.s.s at its point of contact with the wire seemed considerably corroded; and I was confirmed in my idea of referring the production of the alkali princ.i.p.ally to this source, by finding that no fixed saline matter could be obtained by electrifying distilled water in a single agate cup from two points of platina with the Voltaic battery.

"Mr. Sylvester, however, in a paper published in Mr. Nicholson's journal for last August, states that though no fixed alkali or muriatic acid appears when a single vessel is employed, yet that they are both formed when two vessels are used. And to do away with all objections with regard to vegetable substances or gla.s.s, he conducted his process in a vessel made of baked tobacco-pipe clay inserted in a crucible of platina. I have no doubt of the correctness of his results; but the conclusion appears objectionable. He conceives, that he obtained fixed alkali, because the fluid after being heated and evaporated left a matter that tinged turmeric brown, which would have happened had it been lime, a substance that exists in considerable quant.i.ties in all pipe-clay; and even allowing the presence of fixed alkali, the materials employed for the manufacture of tobacco-pipes are not at all such as to exclude the combinations of this substance.

"I resumed the inquiry; I procured small cylindrical cups of agate of the capacity of about one-quarter of a cubic inch each. They were boiled for some hours in distilled water, and a piece of very white and transparent amianthus that had been treated in the same way was made then to connect together; they were filled with distilled water and exposed by means of two platina wires to a current of electricity, from one hundred and fifty pairs of plates of copper and zinc four inches square, made active by means of solution of alum. After forty-eight hours the process was examined: Paper tinged with litmus plunged into the tube containing the transmitting or positive wire was immediately strongly reddened. Paper colored by turmeric introduced into the other tube had its color much deepened; the acid matter gave a very slight degree of turgidness to solution of nitrate of soda. The fluid that affected turmeric retained this property after being strongly boiled; and it appeared more vivid as the quant.i.ty became reduced by evaporation; carbonate of ammonia was mixed with it, and the whole dried and exposed to a strong heat; a minute quant.i.ty of white matter remained, which, as far as my examinations could go, had the properties of carbonate of soda. I compared it with similar minute portions of the pure carbonates of potash, and similar minute portions of the pure carbonates of potash and soda. It was not so deliquescent as the former of these bodies, and it formed a salt with nitric acid, which, like nitrate of soda, soon attracted moisture from a damp atmosphere and became fluid.

"This result was unexpected, but it was far from convincing me that the substances which were obtained were generated. In a similar process with gla.s.s tubes, carried on under exactly the same circ.u.mstances and for the same time, I obtained a quant.i.ty of alkali which must have been more than twenty times greater, but no traces of muriatic acid. There was much probability that the agate contained some minute portion of saline matter, not easily detected by chemical a.n.a.lysis, either in combination or intimate cohesion in its pores. To determine this, I repeated this a second, a third, and a fourth time. In the second experiment turbidness was still produced by a solution of nitrate of silver in the tube containing the acid, but it was less distinct; in the third process it was barely perceptible; and in the fourth process the two fluids remained perfectly clear after the mixture. The quant.i.ty of alkaline matter diminished in every operation; and in the last process, though the battery had been kept in great activity for three days, the fluid possessed, in a very slight degree, only the power of acting on paper tinged with turmeric; but its alkaline property was very sensible to litmus paper slightly reddened, which is a much more delicate test; and after evaporation and the process by carbonate of ammonia, a barely perceptible quant.i.ty of fixed alkali was still left. The acid matter in the other tube was abundant; its taste was sour; it smelled like water over which large quant.i.ties of nitrous gas have been long kept; it did not effect solution of muriate of barytes; and a drop of it placed upon a polished plate of silver left, after evaporation, a black stain, precisely similar to that produced by extremely diluted nitrous acid.

"After these results I could no longer doubt that some saline matter existing in the agate tubes had been the source of the acid matter capable of precipitating nitrate of silver and much of the alkali. Four additional repet.i.tions of the process, however, convinced me that there was likewise some other cause for the presence of this last substance; for it continued to appear to the last in quant.i.ties sufficiently distinguishable, and apparently equal in every case. I had used every precaution, I had included the tube in gla.s.s vessels out of the reach of the circulating air; all the acting materials had been repeatedly washed with distilled water; and no part of them in contact with the fluid had been touched by the fingers.

"The only substance that I could now conceive as furnis.h.i.+ng the fixed alkali was the water itself. This water appeared pure by the tests of nitrate of silver and muriate of barytes; but potash of soda, as is well known, rises in small quant.i.ties in rapid distillation; and the New River water which I made use of contains animal and vegetable impurities, which it was easy to conceive might furnish neutral salts capable of being carried over in vivid ebullition."(1) Further experiment proved the correctness of this inference, and the last doubt as to the origin of the puzzling chemical was dispelled.

Though the presence of the alkalies and acids in the water was explained, however, their respective migrations to the negative and positive poles of the battery remained to be accounted for. Davy's cla.s.sical explanation a.s.sumed that different elements differ among themselves as to their electrical properties, some being positively, others negatively, electrified. Electricity and "chemical affinity," he said, apparently are manifestations of the same force, acting in the one case on ma.s.ses, in the other on particles. Electro-positive particles unite with electro-negative particles to form chemical compounds, in virtue of the familiar principle that opposite electricities attract one another. When compounds are decomposed by the battery, this mutual attraction is overcome by the stronger attraction of the poles of the battery itself.

This theory of binary composition of all chemical compounds, through the union of electro-positive and electro-negative atoms or molecules, was extended by Berzelius, and made the basis of his famous system of theoretical chemistry. This theory held that all inorganic compounds, however complex their composition, are essentially composed of such binary combinations. For many years this view enjoyed almost undisputed sway. It received what seemed strong confirmation when Faraday showed the definite connection between the amount of electricity employed and the amount of decomposition produced in the so-called electrolyte. But its claims were really much too comprehensive, as subsequent discoveries proved.

ORGANIC CHEMISTRY AND THE IDEA OF THE MOLECULE

When Berzelius first promulgated his binary theory he was careful to restrict its unmodified application to the compounds of the inorganic world. At that time, and for a long time thereafter, it was supposed that substances of organic nature had some properties that kept them aloof from the domain of inorganic chemistry. It was little doubted that a so-called "vital force" operated here, replacing or modifying the action of ordinary "chemical affinity." It was, indeed, admitted that organic compounds are composed of familiar elements--chiefly carbon, oxygen, hydrogen, and nitrogen; but these elements were supposed to be united in ways that could not be imitated in the domain of the non-living. It was regarded almost as an axiom of chemistry that no organic compound whatever could be put together from its elements--synthesized--in the laboratory. To effect the synthesis of even the simplest organic compound, it was thought that the "vital force" must be in operation.

Therefore a veritable sensation was created in the chemical world when, in the year 1828, it was announced that the young German chemist, Friedrich Wohler, formerly pupil of Berzelius, and already known as a coming master, had actually synthesized the well-known organic product urea in his laboratory at Sacrow. The "exception which proves the rule"

is something never heard of in the domain of logical science. Natural law knows no exceptions. So the synthesis of a single organic compound sufficed at a blow to break down the chemical barrier which the imagination of the fathers of the science had erected between animate and inanimate nature. Thenceforth the philosophical chemist would regard the plant and animal organisms as chemical laboratories in which conditions are peculiarly favorable for building up complex compounds of a few familiar elements, under the operation of universal chemical laws.

The chimera "vital force" could no longer gain recognition in the domain of chemistry.

Now a wave of interest in organic chemistry swept over the chemical world, and soon the study of carbon compounds became as much the fas.h.i.+on as electrochemistry had been in the, preceding generation.

Foremost among the workers who rendered this epoch of organic chemistry memorable were Justus Liebig in Germany and Jean Baptiste Andre Dumas in France, and their respective pupils, Charles Frederic Gerhardt and Augustus Laurent. Wohler, too, must be named in the same breath, as also must Louis Pasteur, who, though somewhat younger than the others, came upon the scene in time to take chief part in the most important of the controversies that grew out of their labors.

Several years earlier than this the way had been paved for the study of organic substances by Gay-Lussac's discovery, made in 1815, that a certain compound of carbon and nitrogen, which he named cyanogen, has a peculiar degree of stability which enables it to retain its ident.i.ty and enter into chemical relations after the manner of a simple body. A year later Ampere discovered that nitrogen and hydrogen, when combined in certain proportions to form what he called ammonium, have the same property. Berzelius had seized upon this discovery of the compound radical, as it was called, because it seemed to lend aid to his dualistic theory. He conceived the idea that all organic compounds are binary unions of various compound radicals with an atom of oxygen, announcing this theory in 1818. Ten years later, Liebig and Wohler undertook a joint investigation which resulted in proving that compound radicals are indeed very abundant among organic substances. Thus the theory of Berzelius seemed to be substantiated, and organic chemistry came to be defined as the chemistry of compound radicals.

But even in the day of its seeming triumph the dualistic theory was destined to receive a rude shock. This came about through the investigations of Dumas, who proved that in a certain organic substance an atom of hydrogen may be removed and an atom of chlorine subst.i.tuted in its place without destroying the integrity of the original compound--much as a child might subst.i.tute one block for another in its play-house. Such a subst.i.tution would be quite consistent with the dualistic theory, were it not for the very essential fact that hydrogen is a powerfully electro-positive element, while chlorine is as strongly electro-negative. Hence the compound radical which united successively with these two elements must itself be at one time electro-positive, at another electro-negative--a seeming inconsistency which threw the entire Berzelian theory into disfavor.

In its place there was elaborated, chiefly through the efforts of Laurent and Gerhardt, a conception of the molecule as a unitary structure, built up through the aggregation of various atoms, in accordance with "elective affinities" whose nature is not yet understood A doctrine of "nuclei" and a doctrine of "types" of molecular structure were much exploited, and, like the doctrine of compound radicals, became useful as aids to memory and guides for the a.n.a.lyst, indicating some of the plans of molecular construction, though by no means penetrating the mysteries of chemical affinity. They are cla.s.sifications rather than explanations of chemical unions. But at least they served an important purpose in giving definiteness to the idea of a molecular structure built of atoms as the basis of all substances. Now at last the word molecule came to have a distinct meaning, as distinct from "atom," in the minds of the generality of chemists, as it had had for Avogadro a third of a century before. Avogadro's hypothesis that there are equal numbers of these molecules in equal volumes of gases, under fixed conditions, was revived by Gerhardt, and a little later, under the champions.h.i.+p of Cannizzaro, was exalted to the plane of a fixed law.

Thenceforth the conception of the molecule was to be as dominant a thought in chemistry as the idea of the atom had become in a previous epoch.

CHEMICAL AFFINITY

Of course the atom itself was in no sense displaced, but Avogadro's law soon made it plain that the atom had often usurped territory that did not really belong to it. In many cases the chemists had supposed themselves dealing with atoms as units where the true unit was the molecule. In the case of elementary gases, such as hydrogen and oxygen, for example, the law of equal numbers of molecules in equal s.p.a.ces made it clear that the atoms do not exist isolated, as had been supposed.

Since two volumes of hydrogen unite with one volume of oxygen to form two volumes of water vapor, the simplest mathematics show, in the light of Avogadro's law, not only that each molecule of water must contain two hydrogen atoms (a point previously in dispute), but that the original molecules of hydrogen and oxygen must have been composed in each case of two atoms---else how could one volume of oxygen supply an atom for every molecule of two volumes of water?

What, then, does this imply? Why, that the elementary atom has an avidity for other atoms, a longing for companions.h.i.+p, an "affinity"--call it what you will--which is bound to be satisfied if other atoms are in the neighborhood. Placed solely among atoms of its own kind, the oxygen atom seizes on a fellow oxygen atom, and in all their mad dancings these two mates cling together--possibly revolving about each other in miniature planetary orbits. Precisely the same thing occurs among the hydrogen atoms. But now suppose the various pairs of oxygen atoms come near other pairs of hydrogen atoms (under proper conditions which need not detain us here), then each oxygen atom loses its attachment for its fellow, and flings itself madly into the circuit of one of the hydrogen couplets, and--presto!--there are only two molecules for every three there were before, and free oxygen and hydrogen have become water. The whole process, stated in chemical phraseology, is summed up in the statement that under the given conditions the oxygen atoms had a greater affinity for the hydrogen atoms than for one another.

As chemists studied the actions of various kinds of atoms, in regard to their unions with one another to form molecules, it gradually dawned upon them that not all elements are satisfied with the same number of companions. Some elements ask only one, and refuse to take more; while others link themselves, when occasion offers, with two, three, four, or more. Thus we saw that oxygen forsook a single atom of its own kind and linked itself with two atoms of hydrogen. Clearly, then, the oxygen atom, like a creature with two hands, is able to clutch two other atoms.

But we have no proof that under any circ.u.mstances it could hold more than two. Its affinities seem satisfied when it has two bonds. But, on the other hand, the atom of nitrogen is able to hold three atoms of hydrogen, and does so in the molecule of ammonium (NH3); while the carbon atom can hold four atoms of hydrogen or two atoms of oxygen.

Evidently, then, one atom is not always equivalent to another atom of a different kind in combining powers. A recognition of this fact by Frankland about 1852, and its further investigation by others (notably A. Kekule and A. S. Couper), led to the introduction of the word equivalent into chemical terminology in a new sense, and in particular to an understanding of the affinities or "valency" of different elements, which proved of the most fundamental importance. Thus it was shown that, of the four elements that enter most prominently into organic compounds, hydrogen can link itself with only a single bond to any other element--it has, so to speak, but a single hand with which to grasp--while oxygen has capacity for two bonds, nitrogen for three (possibly for five), and carbon for four. The words monovalent, divalent, trivalent, tretrava-lent, etc., were coined to express this most important fact, and the various elements came to be known as monads, diads, triads, etc. Just why different elements should differ thus in valency no one as yet knows; it is an empirical fact that they do. And once the nature of any element has been determined as regards its valency, a most important insight into the possible behavior of that element has been secured. Thus a consideration of the fact that hydrogen is monovalent, while oxygen is divalent, makes it plain that we must expect to find no more than three compounds of these two elements--namely, H--O--(written HO by the chemist, and called hydroxyl); H--O--H (H2O, or water), and H--O--O--H (H2O2, or hydrogen peroxide). It will be observed that in the first of these compounds the atom of oxygen stands, so to speak, with one of its hands free, eagerly reaching out, therefore, for another companion, and hence, in the language of chemistry, forming an unstable compound. Again, in the third compound, though all hands are clasped, yet one pair links oxygen with oxygen; and this also must be an unstable union, since the avidity of an atom for its own kind is relatively weak. Thus the well-known properties of hydrogen peroxide are explained, its easy decomposition, and the eagerness with which it seizes upon the elements of other compounds.

But the molecule of water, on the other hand, has its atoms arranged in a state of stable equilibrium, all their affinities being satisfied.

Each hydrogen atom has satisfied its own affinity by clutching the oxygen atom; and the oxygen atom has both its bonds satisfied by clutching back at the two hydrogen atoms. Therefore the trio, linked in this close bond, have no tendency to reach out for any other companion, nor, indeed, any power to hold another should it thrust itself upon them. They form a "stable" compound, which under all ordinary circ.u.mstances will retain its ident.i.ty as a molecule of water, even though the physical ma.s.s of which it is a part changes its condition from a solid to a gas from ice to vapor.

But a consideration of this condition of stable equilibrium in the molecule at once suggests a new question: How can an aggregation of atoms, having all their affinities satisfied, take any further part in chemical reactions? Seemingly such a molecule, whatever its physical properties, must be chemically inert, incapable of any atomic readjustments. And so in point of fact it is, so long as its component atoms cling to one another unremittingly. But this, it appears, is precisely what the atoms are little p.r.o.ne to do. It seems that they are fickle to the last degree in their individual attachments, and are as p.r.o.ne to break away from bondage as they are to enter into it. Thus the oxygen atom which has just flung itself into the circuit of two hydrogen atoms, the next moment flings itself free again and seeks new companions. It is for all the world like the incessant change of partners in a rollicking dance. This incessant dissolution and reformation of molecules in a substance which as a whole remains apparently unchanged was first fully appreciated by Ste.-Claire Deville, and by him named dissociation. It is a process which goes on much more actively in some compounds than in others, and very much more actively under some physical conditions (such as increase of temperature) than under others. But apparently no substances at ordinary temperatures, and no temperature above the absolute zero, are absolutely free from its disturbing influence. Hence it is that molecules having all the valency of their atoms fully satisfied do not lose their chemical activity--since each atom is momentarily free in the exchange of partners, and may seize upon different atoms from its former partners, if those it prefers are at hand.

While, however, an appreciation of this ceaseless activity of the atom is essential to a proper understanding of its chemical efficiency, yet from another point of view the "saturated" molecule--that is, the molecule whose atoms have their valency all satisfied--may be thought of as a relatively fixed or stable organism. Even though it may presently be torn down, it is for the time being a completed structure; and a consideration of the valency of its atoms gives the best clew that has. .h.i.therto been obtainable as to the character of its architecture.

How important this matter of architecture of the molecule--of s.p.a.ce relations of the atoms--may be--was demonstrated as long ago as 1823, when Liebig and Wohler proved, to the utter bewilderment of the chemical world, that two substances may have precisely the same chemical const.i.tution--the same number and kind of atoms--and yet differ utterly in physical properties. The word isomerism was coined by Berzelius to express this anomalous condition of things, which seemed to negative the most fundamental truths of chemistry. Naming the condition by no means explained it, but the fact was made clear that something besides the mere number and kind of atoms is important in the architecture of a molecule. It became certain that atoms are not thrown together haphazard to build a molecule, any more than bricks are thrown together at random to form a house.

How delicate may be the gradations of architectural design in building a molecule was well ill.u.s.trated about 1850, when Pasteur discovered that some carbon compounds--as certain sugars--can only be distinguished from one another, when in solution, by the fact of their twisting or polarizing a ray of light to the left or to the right, respectively. But no inkling of an explanation of these strange variations of molecular structure came until the discovery of the law of valency. Then much of the mystery was cleared away; for it was plain that since each atom in a molecule can hold to itself only a fixed number of other atoms, complex molecules must have their atoms linked in definite chains or groups. And it is equally plain that where the atoms are numerous, the exact plan of grouping may sometimes be susceptible of change without doing violence to the law of valency. It is in such cases that isomerism is observed to occur.