Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Chemical change classes

In the first century of "organic" chemistry much attention was given to the structures of carbogens and their transformations. Reactions were classified according to the types of substrates that underwent the chemical change (for example "aromatic substitution," "carbonyl addition," "halide displacement," "ester condensation"). Chemistry was taught and learned as transformations characteristic of a structural class (e.g. phenol, aldehyde) or structural subunit... [Pg.5]

Enzyme reactions, like all chemical events, are dynamic. Information coming to us from experiments is not dynamic even though the intervals of time separating observations may be quite small. In addition, much information is denied to us because of technological limitations in the detection of chemical changes. Our models would be improved if we could observe and record all concentrations at very small intervals of time. One approach to this information lies in the creation of a model in which we know all of the concentrations at any time and know something of the structural attributes of each ingredient. A class of models based on computer simulations, such as molecular dynamics, Monte Carlo simulations, and cellular automata, offer such a possibility. [Pg.140]

Tracers have been used to label fluids in order to track fluid movement and monitor chemical changes of the injected fluid. Radioactive materials are one class of commonly used tracers. These tracers have several drawbacks. One drawback is that they require special handling because of the danger posed to personnel and the environment. Another drawback is the alteration by the radioactive materials of the natural isotope ratio indigenous to the reservoir— thereby interfering with scientific analysis of the reservoir fluid characteristics. In addition, the half life of radioactive tracers tends to be either too long or too short for practical use. [Pg.227]

Note Groups 1 to 5 were included in Chapter 5, while Groups 6 to 10 are described in this chapter. They are difficult to place strictly in classes even of chemotypes but the time and increase of appearance follows the chemical changes of the environment over at least 3 billion years. [Pg.243]

The alchemists believed that a most minute proportion of the Stone projected upon considerable quantities of heated mercury, molten lead, or other "base" metal, would transmute practically the whole into silver or gold. This claim of the alchemists, that a most minute quantity of the Stone was sufficient to transmute considerable quantities of base" metal, has been the object of much ridicule. Certainly, some of the claims of the alchemists (understood literally) are out of all reason but on the other hand, the disproportion between the quantities of Stone and transmuted metal cannot be advanced as an a priori objection to the alchemists claims, inasmuch that a class of chemical reactions (called "catalytic") is known, in which the presence of a small quantity of some appropriate form of matter — the catalyst — brings about a chemical change in an indefinite quantity of some other form or forms thus, for example, cane-sugar in aqueous solution is converted into two other sugars by the action of small quantities of acid and sulphur-dioxide and oxygen, which will not combine under ordinary conditions, do so readily in the presence of a small quantity... [Pg.31]

Chemical changes proceed toward a condition called chemical equilibrivun, which represents the lowest energy state for a reactant/product system. In seawater, an important class of reactions that achieve equilibrium are those that can be represented by Eq. 5.3,... [Pg.111]

For simplicity we will assume that only one gas takes part in the chemical change. Unretarded reactions, and reactions retarded by the presence of their products, must be considered separately, because there are important differences between the results for these two classes. [Pg.232]

The present article reviews the photochemical deactivation modes and properties of electronically excited metallotetrapyrroles. Of the wide variety of complexes possessing a tetrapyrrole ligand and their highly structured systems, the subject of this survey is mainly synthetic complexes of porphyrins, chlorins, corrins, phthalocyanines, and naphthalocyanines. All known types of photochemical reactions of excited metallotetrapyrroles are classified. As criteria for the classification, both the nature of the primary photochemical step and the net overall chemical change, are taken. Each of the classes is exemplified by several recent results, and discussed. The data on exciplex and excimer formation processes involving excited metallotetrapyrroles are included. Various branches of practical utilization of the photochemical and photophysical properties of tetrapyrrole complexes are shown. Motives for further development and perspectives in photochemistry of metallotetrapyrroles are evaluated. [Pg.135]

After classifying the chemical changes that produced the whiting compounds, explain the reason for placing each chemical change in a particular class. [Pg.124]

A system is needed to organize chemical changes after they are identified. If one knows the class for a chemical change, the outcome or products produced can be predicted. Most but not all chemical changes fit into one of the four classes. [Pg.145]

Electronic conductance is characteristic for the so called conductors of the first class, i. e. for metals (both in solid and fused state) and some metal oxydes, carbides, sulphides, phosphides and borides and it can be explained by assuming the existence of free electrons which act in solid matter as anions. Under the influence of the external electric field these easily movable electrons start an ordered motion while the atoms deprived of their electrons, which are in fact cations, take practically no part in the current conduction and, apart from their vibration within the mean equilibrium positions, remain practically immobile. The passage of the current does not manifest itself by a chemical change of the... [Pg.17]

Definitions. — An Oxide is a compound of oxygen and one other element, such as iron, zinc, or lead. Chemical action is a term applied to all classes of chemical changes, such as the addition of oxygen to iron, or the decomposition of the red powder into oxygen and mercury. The... [Pg.22]

Summarizing, it may be stated that the combination of size, shape, degree of sulfation, and distribution of sulfate groups endows heparin with a specific, anticoagulant activity of a type which may be different from that shown by synthetic, sulfated polysaccharides," and that inactivation appears to take place with relatively little chemical change in the molecule. The sulfation of heparin may well result in its conversion to the class of synthetic, sulfated mucopolysaccharides. [Pg.367]


See other pages where Chemical change classes is mentioned: [Pg.212]    [Pg.358]    [Pg.175]    [Pg.175]    [Pg.135]    [Pg.313]    [Pg.582]    [Pg.271]    [Pg.186]    [Pg.369]    [Pg.4]    [Pg.218]    [Pg.202]    [Pg.438]    [Pg.153]    [Pg.313]    [Pg.69]    [Pg.248]    [Pg.568]    [Pg.6]    [Pg.123]    [Pg.126]    [Pg.138]    [Pg.635]    [Pg.162]    [Pg.118]    [Pg.96]    [Pg.317]    [Pg.19]    [Pg.72]    [Pg.533]    [Pg.125]    [Pg.7]    [Pg.61]    [Pg.26]   
See also in sourсe #XX -- [ Pg.127 ]




SEARCH



Chemical changes

© 2024 chempedia.info