It remains, therefore, to consider Erlenmeyer's formula and those derived from the centric hypothesis.
On the centric hypothesis two formulae are possible: (1) due to H.E.
When, as in the formation of naphthalene tetrachloride, for example, the one ring becomes saturated, the other might be expected to assume the normal centric form and become relatively inactive.
The centric formula proposed by Bamberger represents naphthalene as formed by the fusion of two benzene rings, this indicates that it is a monocyclic composed of ten atoms of carbon.
According to Armstrong, anthracene behaves unsymmetrically towards substituents, and hence one lateral ring differs from the other; he represents the molecule as consisting of one centric ring, the remaining medial and lateral ring being ethenoid.
Then, on account of the relatively slight - because divided - influence which would be exercised upon the two rings by the two affinities common to both, the remaining four centric affinities of each ring would presumably be less attracted into the ring than in the case of benzene; consequently they would be more active outwards, and combination would set in more readily.
In this formula, the so-called " centric formula," the assumption made is that the fourth valencies are simply directed towards the centre of the ring; nothing further is said about the fourth valencies except that they exert a pressure towards the centre.
Bamberger (a strong supporter of the centric formula), have shown that the nature of the substituent groups influences the distribution of the fourth valencies; therefore it may be con-?
The centric hypothesis has been applied to these rings by Bamberger and others; but as in the previous rings considered, the ordinary (3) (4) (5) representation with double and single linkages generally represents the syntheses, decompositions, &c.; exceptions, however, are known where it is necessary to assume an oscillation of the double linkage.
While those which are cylindrical or of similar shape (centric leaves) have it all round.