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Polar molecules definition

Electro-osmosis has been defined in the literature in many indirect ways, but the simplest definition comes from the Oxford English Dictionary, which defines it as the effect of an external electric held on a system undergoing osmosis or reverse osmosis. Electro-osmosis is not a well-understood phenomenon, and this especially apphes to polar non-ionic solutions. Recent hterature and many standard text and reference books present a rather confused picture, and some imply directly or indirectly that it cannot take place in uniform electric fields [31-35]. This assumption is perhaps based on the fact that the interaction of an external electric held on a polar molecule can produce only a net torque, but no net force. This therefore appears to be an ideal problem for molecular simulation to address, and we will describe here how molecular simulation has helped to understand this phenomenon [26]. Electro-osmosis has many important applications in both the hfe and physical sciences, including processes as diverse as water desahnation, soil purification, and drug delivery. [Pg.786]

The three polar molecules in the series are interesting because they all have anomalous directions to their dipole moments, i.e., the direction is different from that predicted by an elementary application of the idea of electronegativity, accepting the fact that there may be ambiguity in the definition of electronegativity for Ne. We will see how VB ideas interpret these anomalous dipole moments. [Pg.162]

Such a calculation had to be made in determining the problem of interaction between a diatomic polar molecule and an atom with a closed electronic shell [1,2]. The solution of this problem was of special importance in connection with the nature of the hydrogen bond. Our investigations were based on a definite hydrogen bond model that was verified by mathematical treatment and comparison with experimental results. This model is essentially different from that criticized by Dr. Burawoy. Its main point can be explained as follows [2, 3]. [Pg.391]

Poison(s). See also Insecticides, Antibiotics, Inhibitors cyanide 590 hydroxylamine 590 Polar membrane 5 Polar molecules 50 definition of 48 hydration of 50 Polarizability 590... [Pg.928]

This has been studied much less frequently and appears to be a rather more complex reaction. The first results obtained, for the butyl-lithium, styrene reaction in benzene have already been described. In a similar way the addition of butyllithium to 1,1-diphenylethylene shows identical kinetic behaviour in benzene (26). Even the proton extraction reaction with fluorene shows the typical one-sixth order in butyllithium (27). It appears therefore that in benzene solution at least, lithium alkyls react via a small equilibrium concentration of unassociated alkyl. This will of course not be true for reactions with polar molecules for reasons which will be apparent later. No definite information can be obtained on the dissociation process. It is possible that the hexamer dissociates completely on removal of one molecule or that a whole series of penta-mers, tetramers etc. exist in equilibrium. As long as equilibrium is maintained, the hexamer is the major species present and only monomeric butyllithium is reactive, the reaction order will be one-sixth. A plausible... [Pg.77]

Many substances, particularly polar molecules, cross membranes at rates greater than those predicted from solubility and permeability data. Some can cross membranes against a concentration gradient. Unexpectedly high membrane permeability is related to transport proteins. Many transport proteins have been identified, cloned, and sequenced. Current knowledge has permitted an operational definition of carrier proteins as channels, carriers, and pumps. The current state of the art in identification and characterization of these systems has been described by Wright. ... [Pg.26]

In general, less polar solutes dissolve best in solvents with low values, and the higher values favor dissolution of polar molecules. However, the involvements of specific interactions, especially hydrogen bonding, do not allow definite trends to be established which relate the extent to which a solute is dissolved to the polarity of the solute and the relative permittivity of the solvent (Snyder, 1978). [Pg.337]

Van der Waals forces represent important intermolecular interactions between nonelectrolyte substances, and can be categorized into dipole-dipole, dipole-induced-dipole, and induced-dipole-induced-dipole forces. Polar molecules, by definition, will have a permanent dipole moment, and will interact with the oppositely charged portions or other molecules having permanent dipole moments. The dipole-dipole interaction is known as the orientation effect, or as the Keesom force. [Pg.15]

For example, hydrochloric acid is produced by dissolving hydrogen chloride gas, HCl, in water. Remember from Chapter 13 that water is a polar molecule that is able to form strong hydrogen bonds with solutes that also form hydrogen bonds. When HCl dissolves in water, it produces hydronimn ions by the reaction shown below. HCl is definitely an acid it produces H3O+ when dissolved in water. [Pg.485]

On the other hand, by definition, the polarization at an instant t = 0 after a strong collision is determined by the total dipole moment of a unit volume, comprising N polar molecules ... [Pg.502]

A polar molecule in solution can polarize the surrounding medium giving rise to an electric field, the reaction field (i ) at the solute. In a definitive paper, Buckingham" has developed a theory of the effect of the reaction field on chemical shifts based on the Onsager model. ... [Pg.88]

The steady-state fluorescence anisotropy/polarization method is also simple and relies on the fact that the probe molecule will tumble rapidly in solution when free, but will have restricted motion upon binding to a macromolecule. Optical excitation of the probe by polarized light will result in preferential absorption by those molecules whose absorption transition dipole is parallel to the electric field vector direction of the light. The subsequent fluorescence will be partially polarized. The definitions of anisotropy (r) and polarization (P) are [188]... [Pg.172]


See other pages where Polar molecules definition is mentioned: [Pg.438]    [Pg.290]    [Pg.133]    [Pg.74]    [Pg.568]    [Pg.102]    [Pg.413]    [Pg.39]    [Pg.260]    [Pg.336]    [Pg.41]    [Pg.94]    [Pg.160]    [Pg.5]    [Pg.45]    [Pg.14]    [Pg.61]    [Pg.66]    [Pg.49]    [Pg.30]    [Pg.259]    [Pg.193]    [Pg.56]    [Pg.204]    [Pg.160]    [Pg.294]    [Pg.22]    [Pg.32]    [Pg.149]    [Pg.1]    [Pg.136]   
See also in sourсe #XX -- [ Pg.48 ]

See also in sourсe #XX -- [ Pg.48 ]

See also in sourсe #XX -- [ Pg.48 ]

See also in sourсe #XX -- [ Pg.48 ]




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