to the processes of fermentation, and the comprehensive group of alcohols, and their derivatives, the ethers and allied compounds. 'In treating these various classes of compounds, the author preferred to examine successively the different members of each homologous group, before passing to the consideration of the derivatives from the typical or leading member of each group. For instance, in the case of ordinary alcohol, instead of describing ether, aldehyd, and acetic acid in succession,—the different varieties of alcohol, such as wood spirit, fousel oil, &c., are first described ; then the series of the vinic acids, and then that of the ethers. By thus presenting the different members of the same homologous series in succession to the student (see p. 40) he is enabled to trace more readily their similarities and their differences, and to note the general method adopted in their preparation, than if his attention were distracted by passing to other bodies of totally different character and properties. This plan conduces to brevity as well as to clearness, and facilitates the description of the various series from a more general point of view, than would be readily practicable, if the arrangement followed by most writers since the appearance of Liebig's classical work on organic chemistry The most important changes in the present edition consist in the adoption of a new form of notation, and in a recurrence in the concluding volume to the system of nomenclature introduced by Berzelius. This nomenclature has been used occasionally ever since it was proposed, but it was not extensively adopted by chemical writers in this country until its merits were prominently insisted upon two or three years ago by Professor Williamson. The substitution of such terms as potassic nitrate for nitrate of potash, sodic sulphate for sulphate of soda, and zincic oxide for oxide of zinc, may, like most changes, appear at first to some extent awkward and pedantic. Yet the system possesses advantages in brevity and precision which will, there can be little doubt, lead to its gradual substitution for the older nomenclature. The change in notation will doubtless be attended with more inconvenience; though it is certain to be adopted, since in none of the recent investigations made in this country, and in very few of those on the Continent, is the old method made use of. It is remarkable that the ratios expressive of atomic weights in the symbols employed by Berzelius, at their first introduction by him nearly fifty years ago, should be, with few exceptions, those to which Cannizzaro and Wurtz with other writers of the present day have returned. In order to facilitate the use of this new notation, a table of the symbols and atomic weights adopted in the present volu me has been prefixed. In a few instances of the more common bodies of the organic kingdom, the old formula has been given by the side of that now preferred. Those symbols which, in consequence of the alteration, have become changed in value, are indicated in the new formulæ by barred letters. It is easy to transform the new values into those formerly adopted by doubling the numbers attached to each of the barred letters, leaving the others unaltered : alcohol, for example, may be represented either as 6,4,9, or as C,H,02. King's COLLEGE, LONDON, October, 1866. TABLE OF CONTENTS. . Organic Analysis_Classification of Organic Bodies—Metamorphoses–Synthesis. 1-89 1035 Difference between Organized and Organic Bodies. 1036 Ordinary Components of Organic Compounds 1037 Difference between Organic and Inorganic Compounds 1038 Frequency of Isomerism in Organic Bodies Ý I. Analysis of Organic Bodies. 1039 A. Proximate Analysis-Desiccation 1040 Fractional Crystallization, Precipitation, Distillation, Solution, 1041 B. Ultimate Analysis--Desiccation 1042 Determination of Saline Constituents 1043 General Principles of Ultimate Analysis 1044 1. Analysis of a Solid free from Nitrogen 1045 2. Analysis of a Liquid free from Nitrogen 1046 3. Analysis of a Compound containing Nitrogen Method of Varrentrapp and Will 1049 Method of Relative Volumes 1050 Determination of Sulphur and of Phosphorus 5051 Determination of Chlorine, Bromine, and Iodine 1052 Determination of the Equivalents of Organic Compounds ib. 1053 Distinction between Combining Proportion and Molecular 1054 Vapour Density-its Theoretical Value 1055 Distinction between Atomic Weight and Molecular Weight . Ø II. Classification of Organic Compounds. 1057 General Principles of Classification NO. OF . 48 . 51 1060 Theory of Compound Radicles 1061 Theory of Isolated Radicles—Atoms—Molecules 1062 Arguments for doubling the Atomic Weight of Oxygen. 1064 Theory of Polybasic Elements 1065 Application of the Theory of Multequivalent Elements . 60 1066 Mode of determining the Equivalency of an Element 1067 Bearing of the law of Multiple Proportion upon the Theory of 1068 Causes of Polybasic Character of Radicles 1069 Influence of Position of the Atoms in a Compound upon its § III. Production of Chemical Metamorphoses. 1070 1. Metamorphosis by Oxidation 1071 2. Metamorphosis by Reduction. 1072 3. Metamorphosis by Substitution 1073 Substitution of Chlorine and its Analogues for Hydrogen 78 The Saccharine, or Amylaceous Group—Different 1076 General Remarks on Sugars, Starch, &c. 1078 1. Cane Sugar, or Sucrose 1079 Action of Bases on Sugar-Metacetone 1080 Other Modes of Decomposition of Sugar 1081 Action of Heat on Sugar-Caramel 1082 Eucalyptus Sugar-Melitose, Eucalyn . 1083 2. Sugar of Milk, or Lactose 1084 3. Grape Sugar, Dextrose or Glucose-Sulpho-saccharic- Glucic-Apoglucic, and Melassic Acids 1085 Quantitative Estimation of Sugar 1086 4. Fruit Sugar, or Lævulose-Inverted Sugar Effects of the various Sugars on Polarized Light 1088. Manufacture of Raw Sugar-Maple Sugar-Beet Root 1090 Action of Nitric Acid upon Sugars—Saccharic-Mucic- Pyromucic and Paramucic Acids |