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Nonpolar, definition

Recently a definitive study of several isoxazol-5-ones using infrared and ultraviolet spectroscopy (Table I) has shown that the balance between the various tautomers is a delicate one and that all three of the structural types can predominate depending upon the nature of the substituents and the conditions of the experiment. However, the hydroxy form is only found when it is stabilized by chelation (i.e., a carbonyl substituent in the 4-position). The other compounds exist in the CH form in nonpolar media increasing polarity of the solvent stabilizes increasing amounts of the more polar NH forms. [Pg.38]

Lipids are naturally occurring organic molecules that have limited solubility in water and can be isolated from organisms by extraction with nonpolar organic solvents. Fats, oils, waxes, many vitamins and hormones, and most nonprotein cell-meznbrane components are examples. Note that this definition differs from the sort used for carbohydrates and proteins in that lipids are defined by a physical property (solubility) rather than by structure. Of the many kinds of lipids, we ll be concerned in this chapter only with a few triacvlglycerols, eicosanoids, terpenoids, and steroids. [Pg.1060]

Unfortunately, relatively little work has been done on the solution thermodynamics of concentrated polymer solutions with "gathering". The definitive work on the subject Is the article of Yamamoto and White (17). The corresponding-states theory of Flory (11) does not account for gathering. We therefore restrict our consideration here to multicomponent solutions where the solvents and polymer are nonpolar. For such solutions, gathering Is unlikely to occur. [Pg.197]

Liquid solvents in this picture may be considered as islands in the northern hemisphere, because the state of molecules in a liquid solvent is quite definitely closer to the COSMO state than to the vacuum. The only exception may be alkane solvents, which are located somewhere close to the equator due to their fully nonpolar character. Solids may be considered as sunken islands and their depths below sea level may be considered as AG s. As discussed before, the methods to explore this depth are rather limited, but we can be quite sure that in general the depth below sea level will be much smaller than the distance of the islands from the North Pole or from each other. We now explore the methods to go from the sea level position of any island to the North Pole or vice versa. Given such a method we will be able to transfer a compound from any liquid or supercooled liquid state to any other such state. [Pg.293]

A comparahve analysis of coefficients and descriptors clarifies the relationship between lipophilicity and hydrophobicity (Y in Eq. 4 is the molar volume which assesses the solute s capacity to elicit nonpolar interactions (i.e. hydrophobic forces) which, as also clearly stated in the International Union of Pure and Applied Chemistry definitions [3] are not synonyms but, when only neutral species are concerned, may be considered as interchangeable. In the majority of partitioning systems, the lipophilicity is chiefly due to the hydrophobicity, as is clearly indicated by the finding that the product of numerical values of the descriptors V and of the coefficient v is larger in absolute value than the corresponding product of other couples of descriptors/coefficients [9]. This explains the very common linear rela-... [Pg.323]

Another pertinent observation is the fact that the reaction proceeded twice as fast in -butyraldehyde (polar) as in benzene (nonpolar), even though the catalyst concentration was reduced to only one-third the comparable level. A graphic illustration of this effect is given in Fig. 9. The rate of gas uptake is plotted as a function of time for a reaction conducted in benzene and again for a second reaction conducted in butyraldehyde. The rate of reaction in the polar solvent was initially fast and decreased with time. The rate in the nonpolar benzene was initially slow, became faster as the solvent became more polar with the presence of product aldehyde, and then subsequently diminished with time. When the data were replotted as the log of unreacted olefin vs. time, the polar medium reaction showed first-order dependence on olefin concentration, whereas the nonpolar solvent reaction showed no definite order, owing to the constantly changing polarity. [Pg.29]

Lipids are naturally occurring organic molecules, isolated from animal or plant cells by extraction with nonpolar organic solvents. This definition defines lipids in terms of a physical property (solubility) and differs from structural definitions used for proteins or carbohydrates. Not surprisingly, lipids are highly varied in their structure from the medicinal chemistry perspective, there are five classes of lipids ... [Pg.471]

Almost all of the reactions that the practicing inotganic chemist observes in the laboratory take place in solution. Although water is the best-known solvent, it is not the only one of importance to the chemist. The organic chemist often uses nonpolar solvents sud) as carbon tetrachloride and benzene to dissolve nonpolar compounds. These are also of interest to Ihe inoiganic chemist and, in addition, polar solvents such as liquid ammonia, sulfuric acid, glacial acetic acid, sulfur dioxide, and various nonmctal halides have been studied extensively. The study of solution chemistry is intimately connected with acid-base theory, and the separation of this material into a separate chapter is merely a matter of convenience. For example, nonaqueous solvents are often interpreted in terms of the solvent system concept, the formation of solvates involve acid-base interactions, and even redox reactions may be included within the (Jsanovich definition of acid-base reactions. [Pg.725]

The suitability of a stationary phase for a specific separation depends upon the selectivity of the phase. This is a measure of the degree to which polar compounds are retarded relative to their elution on a nonpolar phase. A systematic method for expressing the retention data is based on retention indices. For this sytem, the retention indices of the n-paraffins are by definition equal to 100 times the number of carbon atoms in the molecule. For example, the retention index for n-hexane is 600 and for n-octane 800. These values are defined and apply regardless of the column used and regardless of the temperature. [Pg.129]

The ion-selective membrane is the key component of all potentiometric ion sensors. It establishes the preference with which the sensor responds to the ion of interest in the presence of various other ionic components of the sample. By definition, the ion-selective membrane forms a nonpolarized interface with the solution. If the interface is permeable to only one ion, the potential difference at that interface is expressed by the Nernst equation (6.6). If more than one ion can permeate, the interface can be anything between the liquid junction and the mixed potential. The key distinguishing feature is the absolute magnitude of the total exchange current density. [Pg.138]

It may be expected that other, highly structured solvents with a tri-dimensional network of strong hydrogen bonds, would also permit micelle formation by surfactants, but little evidence of such occurrences has been reported. On the other hand, surfactants in non-polar solvents, aliphatic or aromatic hydrocarbons and halocarbons tend to form so-called inverted micelles, but these aggregate in a stepwise manner rather than all at once to a definite average size. In these inverted micelles, formed, e.g., by long-chain alkylammonium salts or dinonyl-naphthalene sulfonates, the hydrophilic heads are oriented towards the interior, the alkyl chains, tails, towards the exterior of the micelles (Shinoda 1978). Water and hydrophilic solutes may be solubilized in these inverted micelles in nonpolar solvents, such as hydrocarbons. [Pg.376]

Lipids. In a geochemical context, lipids are defined as organic compounds that can be extracted with nonpolar organic solvents (e.g., hexane, chloroform, ether) or solvent mixtures (e.g., benzene/methanol) (Breger, 1960). This definition accommodates a diverse group of compounds that includes saturated, unsaturated,... [Pg.113]


See other pages where Nonpolar, definition is mentioned: [Pg.19]    [Pg.127]    [Pg.36]    [Pg.103]    [Pg.203]    [Pg.745]    [Pg.368]    [Pg.133]    [Pg.267]    [Pg.17]    [Pg.125]    [Pg.584]    [Pg.373]    [Pg.399]    [Pg.371]    [Pg.234]    [Pg.83]    [Pg.167]    [Pg.276]    [Pg.391]    [Pg.217]    [Pg.386]    [Pg.336]    [Pg.59]    [Pg.790]    [Pg.2]    [Pg.211]    [Pg.52]    [Pg.191]    [Pg.99]    [Pg.126]    [Pg.95]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.18 , Pg.29 , Pg.48 , Pg.83 ]

See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.18 , Pg.29 , Pg.48 , Pg.83 ]




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