Journal of the Chemical Society, Volume 103,Partie 1Chemical Society., 1913 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
Table des matières
1 | |
19 | |
27 | |
31 | |
36 | |
56 | |
63 | |
71 | |
645 | |
650 | |
662 | |
669 | |
677 | |
686 | |
687 | |
700 | |
78 | |
91 | |
97 | |
104 | |
112 | |
119 | |
127 | |
145 | |
177 | |
191 | |
220 | |
230 | |
238 | |
249 | |
276 | |
284 | |
290 | |
292 | |
296 | |
300 | |
307 | |
317 | |
324 | |
330 | |
340 | |
345 | |
351 | |
361 | |
377 | |
389 | |
399 | |
404 | |
406 | |
419 | |
426 | |
427 | |
433 | |
444 | |
461 | |
469 | |
489 | |
496 | |
508 | |
517 | |
528 | |
536 | |
548 | |
564 | |
575 | |
586 | |
592 | |
594 | |
598 | |
604 | |
613 | |
623 | |
628 | |
636 | |
706 | |
708 | |
710 | |
723 | |
775 | |
781 | |
786 | |
817 | |
837 | |
847 | |
861 | |
871 | |
885 | |
896 | |
897 | |
913 | |
925 | |
934 | |
940 | |
942 | |
959 | |
965 | |
966 | |
973 | |
974 | |
982 | |
989 | |
998 | |
1001 | |
1004 | |
1006 | |
1010 | |
1022 | |
1035 | |
1039 | |
1043 | |
1052 | |
1067 | |
1072 | |
1074 | |
1088 | |
1102 | |
1108 | |
1109 | |
1119 | |
1144 | |
1154 | |
1167 | |
1170 | |
1193 | |
1202 | |
1210 | |
1221 | |
1228 | |
1242 | |
1251 | |
1255 | |
1263 | |
Autres éditions - Tout afficher
Journal of the Chemical Society, Volume 75 Chemical Society (Great Britain) Affichage du livre entier - 1899 |
Journal of the Chemical Society, Volume 52 Chemical Society (Great Britain) Affichage du livre entier - 1887 |
Journal of the Chemical Society, Volume 55 Chemical Society (Great Britain) Affichage du livre entier - 1889 |
Expressions et termes fréquents
absorption acetic acid acetic anhydride acetone actinium alcoholic solution alkali alkaloid ammonium amount anhydride anhydrous aqueous solution atom behaviour benzene benzoyl bismuth boiling bromine c.c. N₂ carbon cent CH₂ chloroform CO₂ colour colourless compound concentrated condensation containing crystallised crystals curves decomposition described dilute dissolved distilled dried ester ether ethyl acetate ethyl acetoacetate ethyl tartrate evaporated excess experimental experiments extracted ferric filtrate formula gave glucoside grams H₂O heated hydrochloric acid hydrogen chloride hydrolysis insoluble iodine isolated isomerides ketone latter light petroleum liquid maximum rotation melting point method methyl alcohol methyl iodide mixture molecular molecule needles nitrite nitrogen obtained oxide oxygen potassium hydroxide precipitate prepared present pressure prisms pure quercetagetin reaction readily requires residue salt separated sodium solid solvent sparingly soluble substance sulphate sulphide sulphuric acid temperature thiosulphate thorium tion tube unsaturated uranium-X viscosity whilst yellow yield
Fréquemment cités
Page 703 - Application was made to the Government Grant Committee of the Royal Society for a grant of £250 for the hire of a vessel.
Page 717 - prepared mind," that is, the mind so gifted with imaginative insight and so fortified by accurate training as to be alert to perceive and quick to seize upon the novel and essential, which is turned at once to unexpected uses. It has been well said that "the discovery which has been pointed to by theory is always one of profound interest and importance, but it is usually the close and crown of a long and fruitful period; whereas the discovery which comes as a puzzled surprise usually marks a fresh...
Page 1137 - ... this grouping in the four atoms or radicals — inactive bodies all different — united to carbon. My conception is, as Baeyer pointed out at the Kekule festival, a continuation of Kekule's law of the quadrivalence of carbon, with the added hypothesis that the four valences are directed towards the corners of a tetrahedron, at the centre of which is the carbon atom. Practically our ideas, so far as they concern the asymmetric carbon, amount to the same thing— explanation of the two isomers...
Page 466 - Proc. (1913), 29, 51) observe that carbon, at all temperatures up to 900° C. and probably above that temperature, has the power of pertinaciously retaining oxygen. This oxygen cannot be removed by exhaustion alone, but may be expelled by increasing the temperature of the carbon during exhaustion.
Page 123 - The expenses of this research have been in part defrayed by a grant from the Government Grant Committee of the Royal Society, for which we desire to express our indebtedness.
Page 384 - The authors wish to acknowledge their thanks to the Carnegie Trust for the Universities of Scotland for a...
Page 198 - The filtered liquid was than concentrated to a small bulk, when a brown product was obtained, but nothing definite could be isolated from it. The filtrate from the basic lead acetate precipitate was...
Page 106 - The solution was acidified and the acid was extracted with ether. The ethereal solution was washed with water, dried over sodium sulfate, filtered, and the ether was distilled off.
Page 149 - Phil. Trans.,' 1912, A, vol. 212, p. 261. J ' Berichte,' pp. 366-408. § 'Zeit. Phys. Chem.,' vol. 60, pp. 563, 590, 641, 756. || An attempt to harmonise qualitatively the relations between temperature and rotation for light of all refrangibilities of certain active substances both in the homogeneous state and in solution, ' Chem. Soc. Trans.,
Page 212 - A mixture of fatty acids, consisting of palmitic, stearic, cerotic, oleic and linolic acids. The alcoholic extract also contained a quantity of sugar, which yielded ^/-phenylglucosazoiie (mp '210°), and a comparatively small amount of resinous material.