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624 SCIENCE. [N. S. VoL. IV. No. 95.

strong mineral acid the final products are ortho- were prepared and studied. When silver and
phosphoric acid and ammonia. If, however, mercury salts of the amides were used, imido-
the action is limited, a series of intermediate ethers were formed and not diacidamides, as
acids is formed. Methods were devised for ob- was expected.
taining these acids in pure condition and a Iodometic Determination of Selenious and Selenic
number of their salts were made and studied. Acids: By J. F. NORRIs and H. FAY. This
On Certain Derivatives of Trichlordinitrobenzol: method depends on the reaction between sodium
By C. LORING JACKSON and W. R. LAMAR. thiosulphate and selenious acid in the presence
The results of an investigation of the behavior of hydrochloric acid. If the selenious acid in
of various reagents with tribromdinitrobenzol the presence of hydrochloric acid is treated
have been published in this JOURNAL. In the with an excess of sodium thiosulphate, and then
present paper the author compares those re- titrated back with iodine, very satisfactory re-
sults with the ones obtained when trichlordini- sults can be obtained. The complete reaction
trobenzol is used. With aniline the reaction in which takes place here is as yet unknown.
both cases is similar, the product formed being Selenic acid must be reduced by boiling with
trianilidodinitrobenzol. When sodic ethylate is hydrochloric acid before the selenium can be
used, the replacement of two bromine or two determined. Mixtures of the two can be easily
chlorine atoms leads to the formation of simi- analyzed by first determining the selenious acid
lar compounds; but the replacement of the and then the total after reduction of the selenic
third does not follow the same rule, nor is the acid. J. ELLIOTT GILPIN.
reaction with malonic acid ester similar in the
two cases. NE W BOOKS.
Camphoric Acid: By W. A. NoYEs. Results
obtained by this author have led him to reject An American Text-Book of Physiology. Edited
the formula proposed for camphor by Bredt, by WILLIAM H. HOWELL. Philadelphia, W.
which is the one most generally accepted, B. Saunders. 1896. Pp. 1052.
and that proposed recently by Tiemann. The Die Bedingungen der Fortpflanzung bei einigen
evidence against the latter is found in the Algen und Pilzen. GEORG KLEBS. Jena, Gus-
fact that the rate of esterification of two com- tav Fischer. 1896. Pp. xviii+543.
pounds, which should according to the view of Die Morphologie und Physiologie des pflanzlichen
Tiemann be the same, is very different. He Zellkernes. A. ZIMMERMANN. Jena, Gustav
has also subjected Armstrong's formula to a Fischer. 1896. Pp. viii+ 188.
synthetic test and finds that his formula for On Certain Problems of Vertebrate Embryology.
camphor is not true. One of the products ob- JOHN BEARD. Jena, Gustav Fischer. 1896.
tained in the course of this investigation, Pp. vi+77. M. 2.
dihydro-cis-campholytic acid, has been studied Evolution of the Art of Music. C. HUBERT
by E. B. Harris, and the results are incorpor- PARRY. New York, D. Appleton & Co. 1896.
ated in this article.
On Diacid Anilides: By H. L. WHEELER. Pp. x+342.
Diacid anilides may be divided into two classes, Alterations of Personality. ALFRED BINET.
the first consisting of those which have identi- Translated by HELEN GREEN BALDWIN. New
cal acid groups, and the second of those with York, D. Appleton & Co. Pp. vii+356.
unlike acid groups. The second class have not Number and its Algebra. ARTHUR LEFEVRE.
been obtained by the same methods as the first; Boston, D. C. Heath & Co. 1896. Pp. 230.
but the author of this paper has devised a The Coming Ice Age. C. A. M. TABER. Bos-
method for their formation, which consists in ton, Geo. H. Ellis. 1896. Pp: 94.
treating silver or mercury acid anilides with an Genius and Degeneration. WILLIAM HIRSCH.
aliphatic acid chloride, when the action is Translated from the second edition of the Ger-
similar to the one in which benzoylchloride is man work. New York, D. Appleton & Co.
used. A number of these mixed diacid anilides 1896. Pp. vi+333.

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