History of Chemistry, Volume 2 (of 2): From 1850 to 1910Thorpe, T. E. (Thomas Edward)
History
History of Chemistry, Volume 2 (of 2): From 1850 to 1910
Thorpe, T. E. (Thomas Edward)
Chemistry -- History
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C══C——C══C——C══C
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From this _closed chain_ all the substances usually designated as
“aromatic compounds” are derived. In these a common nucleus may be
assumed: it is the closed chain C6A6, where A denotes an unsaturated
affinity. The six affinities of this nucleus may be satisfied by six
monovalent elements. They may also, wholly or in part, be satisfied by
one affinity of polyvalent elements, the latter necessarily bringing
with them other atoms into the compound, thus producing one or more
side chains, which in their turn may be lengthened by the addition of
other atoms.
If each of the free units is satisfied by an atom of hydrogen, we
obtain benzene, which, as Kekulé demonstrated, becomes the centre round
which the great group of aromatic compounds might be said to revolve.
Benzene was discovered by Faraday in 1825 among the volatile liquids
condensed from the oil-gas made by the Portable Gas Company. It had
already played a notable part in the development of chemical theory
in connection with the discovery of isomerism. It was now to play a
far more important rôle: to become, in fact, the progenitor of a great
family of substances, not only of theoretical value, but of great
economic importance.
The limits of this work preclude any attempt to trace in detail the
development of the conception with which Kekulé enriched science, or to
dilate upon the great extension of benzenoid or cyclic chemistry which
has resulted from it during the past forty years. It has been said
that Kekulé’s memoir on the benzene theory is the most brilliant piece
of scientific prediction to be found in the whole range of organic
chemistry. Of course, on its promulgation it had to run the gauntlet
of criticism; and an army of eager, active workers was soon engaged in
testing its sufficiency and in developing the rich province which it
first made known. As the facts multiplied, other statical formulæ were
suggested by Dewar, Ladenburg, and Claus, but they have not proved more
adequate to explain the facts as these have become better understood.
Observations which seemed to contradict Kekulé’s theory, or which
seemed to be imperfectly explained by it, have, in the light of fuller
knowledge, been shown to be in harmony with it; and such additional
proofs of agreement have thereby served to strengthen its position.
Its capacity for development is, indeed, as in the case of every
other hypothesis of the first rank, one of its cardinal qualities. It
adequately explains the constitution of great numbers of derivatives
whose analogies and relations, apart from it, would have remained
obscure and in many cases unintelligible. The symmetrical distribution
of the carbon and hydrogen atoms in the benzene molecule, assumed by
Kekulé on indirect grounds, has been established by the independent
investigations of Ladenburg and others, and its ring structure has been
demonstrated by Baeyer and Perkin.
Public-domain text, read in full here on John Shaqi.
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