A Textbook of Organic Chemistry |
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Inhalt
PART I | 1 |
Occurrence Physical properties Chemical character Distillation | 39 |
MONOSUBSTITUTION PRODUCTS OF SATURATED | 45 |
Polyhalogen Compounds | 51 |
Synthesis Amines Amino compounds Basic character | 59 |
PHOSPHORUS AND ARSENIC COMPOUNDS | 64 |
ALKYL ISOCYANATES THIOCYANATES ISOTHIOCYANATES | 73 |
NORMAL PRIMARY ALCOHOLS SATURATED SERIES | 85 |
Isomeric xylenes Ethyl benzene Orientation ortho meta | 486 |
Durene Cymene | 493 |
Illuminating gas Distillation of coal Gaseous products Liquid | 501 |
HALOGEN SUBSTITUTION PRODUCTS OF BENZENE | 507 |
SULPHINIC ACIDS | 523 |
Nitro Benzenes | 530 |
Reduction of nitric acid Reduction of nitro benzene with alcohol | 537 |
DERIVATIVES OF AROMATIC AMINES | 545 |
Methyl AlcoholMethanolWood Alcohol | 94 |
ETHYL ALCOHOL per cent | 101 |
Isomerism Class isomerism Chemical properties | 108 |
ALDEHYDES AND KETONES | 119 |
HOMOLOGOUS SERIES SATURATED ACIDS | 131 |
DERIVATIVES OF ACIDS | 137 |
Esterification Hydrolysis Saponification Names of esters | 144 |
B SIMPLER UNSATURATED COMPOUNDS | 151 |
Homologous series Isomers Chemical properties | 158 |
MONOSUBSTITUTION PRODUCTS OF UNSATURATED | 164 |
Crotonic AldehydeAButenal | 169 |
Tiglic Acid and Angelic Acid | 178 |
Chloroform reaction Ortho formic acid Hofmanns iso nitrile | 184 |
POLYHYDROXY COMPOUNDSPOLYALCOHOLS | 195 |
MIXED POLYSUBSTITUTION PRODUCTS | 220 |
Aldehydealcohols Ketonealcohols | 229 |
Syntheses Alcohollike syntheses From halogen acids From | 241 |
Reactions Anhydrides Pyroracemic acid Stereoisomerism | 251 |
ALDEHYDE ACIDS | 252 |
Preparation of ethyl aceto acetate Tautomerism Enol and keto | 260 |
Salts Esters Acid chlorides Acid amides | 273 |
Synthesis from ethylene bromide From brom acetic acid Diacetic | 280 |
Synthesis from propane From aceto acetic ester From malonic | 287 |
HYDROXY DIBASIC ACIDS | 295 |
Dextro Tartaric Acid | 309 |
Synthesis from glycerol From aceto acetic ester Salts Neutral | 315 |
Oxidation products of polyhydroxyl alcohols Composition and constitu | 323 |
Oxidation to acids Phenyl hydrazine reaction Hydrazones | 329 |
Monosaccharoses Polysaccharoses Disaccharoses or hexobioses | 336 |
TETROSES | 337 |
Number of stereoisomers Table of stereoisomers of glucose | 345 |
Muta rótation alpha and betaMethyl glucosides alpha and beta | 351 |
Constitution of sucrose Sources Industrial processes Extrac | 358 |
General character Solubility Iodine reaction Enzyme action | 363 |
Industrial Uses of Cellulose | 369 |
Cotton and linen cloth etc Paper Wood pulp Production | 379 |
Synthesis from halogen acids From aldehydes From oximes | 386 |
Simple proteins Albumins Globulins Glutelins Prolamins | 399 |
Color reactions Millons reaction Biuret reaction Xanthoproteic | 407 |
CYANIC ACID ISOCYANIC ACID THIOCYANIC | 416 |
CARBONIC ACID UREA URIC ACID PURINE | 425 |
Carbamide Carbamic acid Urethane Biological synthesis | 437 |
Constitution Medicus formula Methyl uric acids Fischer | 446 |
CARBOCYCLIC COMPOUNDS | 460 |
B CARBOCYCLIC COMPOUNDS DERIVED | 466 |
Toluene | 479 |
Diphenyl Amine Triphenyl Amine | 554 |
ANILINO ACIDS | 561 |
Azoxy Benzene | 565 |
Amino Azo Benzene | 573 |
HYDRAZINES | 579 |
Peter Griess Diazotization | 586 |
REACTIONS OF DIAZO COMPOUNDS | 595 |
Poison and antiseptic Commercial preparation | 606 |
Cresols | 613 |
DERIVATIVES OF PHENOLS | 621 |
Quinone oxime Pseudo compounds | 629 |
Molecular rearrangement of hydroxyl amines Photographic reducing | 635 |
B AROMATIC ALCOHOLS | 641 |
AROMATIC ALDEHYDES AND KETONES | 647 |
A ALDEHYDES | 654 |
Anis aldehyde Protocatechuic aldehyde Vanillin Relation | 665 |
Character and type Methyl to carboxyl Oxidation of hydrocarbons | 680 |
Occurrence | 681 |
Toluic Acids Xyloic Acids Mesitylenic Acid | 687 |
Phthalimide Phthalyl chloride meta and paraPhthalic acids | 693 |
Malonic ester synthesis of hydrocinnamic acid Perkins reaction | 699 |
ortholodo benzoic acid | 705 |
From phthalic acid and naphthalene Hofmann reaction Phenyl | 711 |
Synthesis from sulpho benzoic acid From amino benzoic acid From | 720 |
PHENOL SIDECHAIN CARBOXY ACIDS | 726 |
Synthesis from benzene Dinitro diphenyl Benzidine Dianis | 733 |
Methane character Oxidation products Benzene character | 742 |
PHTHALEIN DYES | 750 |
Rhodamines | 756 |
CONDENSED RING COMPOUNDS | 765 |
Coal tar source Constitution Benzene character Yields ortho | 774 |
Synthesis from naphthols alphaNaphthylamine betaNaphthyl | 781 |
Congo red Benzo purpurin Naphthol blue black Fast red B | 789 |
Condensed benzene rings Synthesis from tetrabrom ethane From | 795 |
Turkey red Synthesis by Graebe and Liebermann Reduction | 806 |
Hydro benzenes Quinone and phloroglucinol | 813 |
Geraniol Citral Ionone | 816 |
OXIDATION DERIVATIVES OR CAMPHORS | 825 |
Derivatives of menthene Dihydro carveol Dihydro carvone | 831 |
Thujone Fenchone Constitution of camphor Kompas synthesis | 839 |
HETEROCYCLIC COMPOUNDS | 851 |
CONDENSED HETEROCYCLIC COMPOUNDS | 860 |
ALKALOIDS | 886 |
DIHETEROCYCLIC ALKALOIDS | 892 |
PURINE ALKALOIDS | 900 |
Urheberrecht | |
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A Textbook of Organic Chemistry (Classic Reprint) Joseph Scudder Chamberlain Keine Leseprobe verfügbar - 2018 |
Bibliografische Informationen
| Titel | A Textbook of Organic Chemistry |
| Autor/in | Joseph Scudder Chamberlain |
| Verlag | P. Blakiston's son & Company, 1921 |
| Original von | Harvard University |
| Digitalisiert | 7. März 2007 |
| Länge | 959 Seiten |
| Zitat exportieren | BiBTeX EndNote RefMan |