Groups chemical properties

With all of this work, scientific analysis progressed beyond the generation of analytical data on single specimens to, as stated by Harbottle (1982 14), establishing a group chemical property. In this major review of chemical characterization studies in archaeology, Harbottle lists a wide range of materials that have been studied analytically, but reminded practitioners that ... 

Mendeleef drew up a table of elements considering the chemical properties, notably the valencies, of the elements as exhibited in their oxides and hydrides. A part of Mendeleefs table is shown in Figure 1.2 -note that he divided the elements into vertical columns called groups and into horizontal rows called periods or series. Most of the groups were further divided into sub-groups, for example Groups... 

What are the principal differences in physical and chemical properties between any one metal from Group I and any one metal from Group IV and any one transition metal How far can you explain these differences in terms of their different atomic structures ... 

The chemical properties of the elements in a given group of the Periodic Table change with increasing atomic number. 

Ammonia is a colourless gas at room temperature and atmospheric pressure with a characteristic pungent smell. It is easily liquefied either by cooling (b.p. 240 K) or under a pressure of 8-9 atmospheres at ordinary temperature. Some of its physical and many of its chemical properties are best understood in terms of its structure. Like the other group head elements, nitrogen has no d orbitals available for bond formation and it is limited to a maximum of four single bonds. Ammonia has a basic tetrahedral arrangement with a lone pair occupying one position ... 

Separations based upon differences in the chemical properties of the components. Thus a mixture of toluene and anihne may be separated by extraction with dilute hydrochloric acid the aniline passes into the aqueous layer in the form of the salt, anihne hydrochloride, and may be recovered by neutralisation. Similarly, a mixture of phenol and toluene may be separated by treatment with dilute sodium hydroxide. The above examples are, of comse, simple apphcations of the fact that the various components fah into different solubihty groups (compare Section XI,5). Another example is the separation of a mixture of di-n-butyl ether and chlorobenzene concentrated sulphuric acid dissolves only the w-butyl other and it may be recovered from solution by dilution with water. With some classes of compounds, e.g., unsaturated compounds, concentrated sulphuric acid leads to polymerisation, sulphona-tion, etc., so that the original component cannot be recovered unchanged this solvent, therefore, possesses hmited apphcation. Phenols may be separated from acids (for example, o-cresol from benzoic acid) by a dilute solution of sodium bicarbonate the weakly acidic phenols (and also enols) are not converted into salts by this reagent and may be removed by ether extraction or by other means the acids pass into solution as the sodium salts and may be recovered after acidification. Aldehydes, e.g., benzaldehyde, may be separated from liquid hydrocarbons and other neutral, water-insoluble hquid compounds by shaking with a solution of sodium bisulphite the aldehyde forms a sohd bisulphite compound, which may be filtered off and decomposed with dilute acid or with sodium bicarbonate solution in order to recover the aldehyde. 

For many years the synthesis and chemical properties of allenes has been a major area of interest in this laboratory. In our NMR research group we studied the H and lie behaviour of these compounds. 

The most important chemical property of the carbonyl group is its tendency to undergo nucleophilic addition reactions of the type represented m the general equation... 

In the preceding chapter you learned that nucleophilic addition to the carbonyl group IS one of the fundamental reaction types of organic chemistry In addition to its own reactivity a carbonyl group can affect the chemical properties of aldehydes and ketones m other ways Aldehydes and ketones having at least one hydrogen on a carbon next to the carbonyl are m equilibrium with their enol isomers... 

Substitutive Nomenclature. The first step is to determine the kind of characteristic (functional) group for use as the principal group of the parent compound. A characteristic group is a recognized combination of atoms that confers characteristic chemical properties on the molecule in which it occurs. Carbon-to-carbon unsaturation and heteroatoms in rings are considered nonfunctional for nomenclature purposes. 

Chemical Properties and Industrial Uses. Chloroacetic acid has wide appHcations as an industrial chemical intermediate. Both the carboxyhc acid group and the cx-chlorine are very reactive. It readily forms esters and amides, and can undergo a variety of cx-chlorine substitutions. 

The thermal, electrical, acoustical, and chemical properties of all ceUular polymers are of such a similar nature that the discussions of these properties are not separated kito rigid and flexible groups. 

Formic acid exhibits many of the typical chemical properties of the aHphatic carboxyHc acids, eg, esterification and amidation, but, as is common for the first member of an homologous series, there are distinctive differences in properties between formic acid and its higher homologues. The smaller inductive effect of hydrogen in comparison to an alkyl group leads, for example, to formic acid = 3.74) being a considerably stronger acid than acetic acid... 

Chemical Properties. Trimethylpentanediol, with a primary and a secondary hydroxyl group, enters into reactions characteristic of other glycols. It reacts readily with various carboxyUc acids and diacids to form esters, diesters, and polyesters (40). Some organometaUic catalysts have proven satisfactory for these reactions, the most versatile being dibutyltin oxide. Several weak bases such as triethanolamine, potassium acetate, lithium acetate, and borax are effective as stabilizers for the glycol during synthesis (41). 

Chemical Properties. The chemistry of 1,4-cyclohexanedimethanol is characteristic of general glycol reactions however, its two primary hydroxyl groups give very rapid reaction rates, especially in polyester synthesis. 

Hafnium [7440-58-6] Hf, is in Group 4 (IVB) of the Periodic Table as are the lighter elements zirconium and titanium. Hafnium is a heavy gray-white metallic element never found free in nature. It is always found associated with the more plentiful zirconium. The two elements are almost identical in chemical behavior. This close similarity in chemical properties is related to the configuration of the valence electrons, and for zirconium and... 

Historically, the discovery of one effective herbicide has led quickly to the preparation and screening of a family of imitative chemicals (3). Herbicide developers have traditionally used combinations of experience, art-based approaches, and intuitive appHcations of classical stmcture—activity relationships to imitate, increase, or make more selective the activity of the parent compound. This trial-and-error process depends on the costs and availabiUties of appropriate starting materials, ease of synthesis of usually inactive intermediates, and alterations of parent compound chemical properties by stepwise addition of substituents that have been effective in the development of other pesticides, eg, halogens or substituted amino groups. The reason a particular imitative compound works is seldom understood, and other pesticidal appHcations are not readily predictable. Novices in this traditional, quite random, process requite several years of training and experience in order to function productively. 

Chemical Properties. Its two functional groups permit a wide variety of chemical reactions for lactic acid. The primary classes of these reactions are oxidation, reduction, condensation, and substitution at the alcohol group. 

Chemical Properties. Lignin is subject to oxidation, reduction, discoloration, hydrolysis, and other chemical and enzymatic reactions. Many ate briefly described elsewhere (51). Key to these reactions is the ability of the phenolic hydroxyl groups of lignin to participate in the formation of reactive intermediates, eg, phenoxy radical (4), quinonemethide (5), and phenoxy anion (6) ... 

Reactions. The chemical properties of malonates are highlighted by the acidity of the methylene group (p-R 13) to such an extent that a... 

Reactions. The chemical properties of cyanoacetates ate quite similar to those of the malonates. The carbonyl activity of the ester function is increased by the cyano group s tendency to withdraw electrons. Therefore, amidation with ammonia [7664-41-7] to cyanoacetamide [107-91-5] (55) or with urea to cyanoacetylurea [448-98-2] (56) proceeds very easily. An interesting reaction of cyanoacetic acid is the Knoevenagel condensation with aldehydes followed by decarboxylation which leads to substituted acrylonitriles (57) such as (29), or with ketones followed by decarboxylation with a shift of the double bond to give P,y-unsaturated nitriles (58) such as (30) when cyclohexanone [108-94-1] is used. 

The nature of the alkyl group from the esterifying alcohol, the molecular weight, and the tacticity determine the physical and chemical properties of methacrylate ester polymers. 

Nickel occurs in the first transition row in Group 10 (VIIIB) of the Periodic Table. Some physical properties are given in Table 1 (1 4). Nickel is a high melting point element having a ductile crystal stmcture. Its chemical properties allow it to be combined with other elements to form many alloys. 

Phenol s chemical properties are characterized by the influences of the hydroxyl group and the aromatic ring upon each other. Although the stmcture of phenol is similar to cyclohexanol, phenol is a much stronger acid. Its piC in aqueous solution at 25°C is 9.89 x 10 ° (8). This characteristic allows aqueous hydroxides to convert phenol into their salts. The salts, especially those of sodium and potassium, are converted back into phenol by aqueous mineral acids or carboxyhc acids. 

Chemical Properties. The chemical reactivity of nylon is a function of the amide groups and the amine and carboxyl ends. The aHphatic segment of the chain is relatively stable. 

The chemical properties and reactions of the aminophenols and their derivatives are to be found in detail in many standard chemical texts (25). The acidity of the hydroxyl function is depressed by the presence of an amino group on the benzene ring this phenomenon is most pronounced with 4-aminophenol. 

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