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Polarity, of molecules

Covalent bonds and molecules held together by such bonds may be— [Pg.182]

The two electrons in the H2 molecule are shared equally by the two nuclei. Stated another way, a bonding electron is as likely to be found in the vicinity of one nucleus as another. Bonds of this type are described as nonpolar. Nonpolar bonds are formed whenever the two atoms joined are identical, as in H2 and F2. [Pg.182]

The extent of polarity of a covalent bond is related to the difference in electronegativities of the bonded atoms. If this difference is large, as in HF (AEN = 1.8), the bond is strongly polar. Where the difference is small, as in H—C (AEN = 0.3), the bond is only slightly polar. [Pg.183]

The extent to which molecules tend to orient themselves in an electrical field is a measure of their dipole moment. A polar molecule such as HF has a dipole moment a nonpolar molecule such as H2 or F2 has a dipole moment of zero. [Pg.183]

If a molecule is diatomic, it is easy to decide whether it is polar or nonpolar. A diatomic molecule has only one kind of bond hence the polarity of the molecule is the same as the polarity of the bond. Hydrogen and fluorine (H2, F2) are nonpolar because the bonded atoms are identical and the bond is nonpolar. Hydrogen fluoride, HF, on the other hand, has a polar bond, so the molecule is polar. The bonding electrons spend more time near the fluorine atom so that there is a negative pole at that end and a positive pole at the hydrogen end. This is sometimes indicated by writing [Pg.183]

In the HF molecule, the distribution of the bonding electrons is somewhat different from that in H2 or F2. Here the density of the electron cloud is greater about the fluorine atom. The bonding electrons, on the average, are shifted toward fluorine and away from the hydrogen (atom Y in Figme 7.12). Bonds in which the electron density is unsymmetrical are referred to as polar bonds. [Pg.209]

All molecules, except those of elements, have polar bonds.. [Pg.209]

FIGURE 6.23 (a) A representation of the asymmetrical water molecule, (b) A representation of a symmetrical methane molecule. (From Kenkel, J., Kelter, P., and Hage, D., Chemistry An Industry-Based Introduction with CD-ROM, CRC Press, Boca Raton, FL, 2001. With Permission.) [Pg.159]

5 Given or having determined the Lewis diagram of a molecule, predict whether the molecule is polar or nonpolar. [Pg.378]

A polar covalent bond is defined in Section 12.4 as a bond in which bonding electrons are shared unequally. The charge density of the bonding electrons is shifted toward the more electronegative atom. [Pg.378]

When a molecule has more than two atoms, we must know something about the bond angles in order to decide whether the molecule is polar or nonpolar. Consider, for example, the two triatomic molecules CO2 and H2O. Despite the presence of two [Pg.378]

In contrast, the bent water molecule is polar the two polar bonds do not cancel each other because the molecule is not symmetrical around a horizontal axis (Active Fig. 13.10[b]). The bonding electrons spend more time near the more electronegative oxygen atom, which is the negative pole. The positive pole is midway between the two hydrogen atoms. The molecule is said to be a net dipole. [Pg.379]

From these observations we can state an easy way to decide whether a simple molecule is polar or nonpolar. If the central atom has no lone pairs and all atoms bonded to it are identical, the molecule is nonpolar. If these conditions are not met, the molecule is polar. [Pg.379]

Thus far, we have been concerned with the polarity of one bond. To determine whether a molecule has [Pg.44]

The two molecules HjO and CO2 illustrate different outcomes of this process. In H2O, each 0 -H bond is polar because the electronegativity difference between O (3.4) and H (2.2) is large. Since Fl20 is a bent molecule, the two dipoles reinforce (both point up). Thus, H2O has a net dipole, making it a polar molecule. CO2 also has polar C-O bonds because the electronegativity difference between O (3.4) and C (2.5) is large. However, CO2 is a linear molecule, so the two dipoles, which are equal and opposite in direction, cancel. Thus, CO2 is a nonpolar molecule with no net dipole. [Pg.44]

The net dipole bisects the H—O—H bond angle. The two individual dipoles reinforce. [Pg.44]

Indicate which of the following molecules Is polar because it possesses a net dipole. Show the direction of the net dipole if one exists. [Pg.44]

Besides the properties already deseribed, certain covalent bonds have another property polarity. Two atoms joined by a covalent bond share electrons their nuclei are held by the same electron cloud. But in most cases the two nuclei do not share the electrons equally the electron cloud is denser about one atom than the other. One end of the bond is thus relatively negative and the other end is relatively positive that is, there is a negative pole and a positive pole. Such a bond is said to be a polar bond, or to possess polarity. [Pg.23]

We can indicate polarity by using the symbols 6 + and d, which indicate partial I and — charges. (We say delta plus and delta minus .) For example  [Pg.23]

We can expect a covalent bond to be polar if it joins atoms that differ in their tendency to attract electrons, that is, atoms that differ in electronegativity. Furthermore, the greater the difference in electronegativity, the more polar the bond will be. [Pg.23]

Bond polarities are intimately concerned with both physical and chemical properties. The polarity of bonds can lead to polarity of molecules, and thus profoundly affect melting point, boiling point, and solubility. The polarity of a bond determines the kind of reaction that can take place at that bond, and even affects reactivity at nearby bonds. [Pg.23]

In a wa that cannot be gone into here, it is possible to measure the dipole moments of molecules some of the values obtained are listed in Table 1.4. We shall be interested in the values of dipole moments as indications of the relative polarities of different molecules. [Pg.24]

Whenever C or H is bonded to N, O, and all halogens, the bond is polar. Thus, the C—I bond is considered polar even though the electronegativity difference between C and I is small. Remember, electronegativity is just an approximation. [Pg.46]


The dielectric constant is a property of a bulk material, not an individual molecule. It arises from the polarity of molecules (static dipole moment), and the polarizability and orientation of molecules in the bulk medium. Often, it is the relative permitivity 8, that is computed rather than the dielectric constant k, which is the constant of proportionality between the vacuum permitivity so and the relative permitivity. [Pg.112]

The dielectric permittivity as a function of frequency may show resonance behavior in the case of gas molecules as studied in microwave spectroscopy (25) or more likely relaxation phenomena in soUds associated with the dissipative processes of polarization of molecules, be they nonpolar, dipolar, etc. There are exceptional circumstances of ferromagnetic resonance, electron magnetic resonance, or nmr. In most microwave treatments, the power dissipation or absorption process is described phenomenologically by equation 5, whatever the detailed molecular processes. [Pg.338]

Polarity of bonds can lead to polarity of molecules, as shown in the case of the water molecule ... [Pg.298]

Polarity of molecules. All bonds in these molecules are polar, as shown by ihe - — symbol, in which ihe arrow points to the more negative end of the bond and the + indicates... [Pg.184]

One important stracture in molecules are polar bonds and, as a result, polar molecules. The polarity of molecules had been first formulated by the Dutch physicist Peter Debye (1884-1966) in 1912, as he tried to build a microphysical model to explain dielectricity (the behaviour of an electric field in a substance). Later, he related the polarity of molecules to the interaction between molecules and ions. Together with Erich Hiickel he succeeded in formulating a complete theory about the behaviour of electrolytes (Hofimann, 2006). The discovery of the dipole moment caused high efforts in the research on physical chemistry. On the one hand, methods for determining the dipole momerrt were developed. On the other hand, the correlation between the shape of the molectrle and its dipole moment was investigated (Estermanrr, 1929 Errera Sherrill, 1929). [Pg.233]

Keesom (1879-1956) used the polarity of molecules to explain the viseosity of substanees. [Pg.245]

In typical QM-MM simulations, no dielectric constant is included. Orientational dielectric effects come naturally from reorienting and translation of the elements of the system, providing the system comes to equilibrium. What is left out of the model is electronic polarization of molecules, which makes a minor contribution. [Pg.316]

Gopakumar TG, Meiss J, Pouladsaz D, Hietschold M (2008) HOMO-LUMO gap shrinking reveals tip-induced polarization of molecules in ultrathin layers tip-sample distance-depen-dent scanning tunneling spectroscopy on d8 (Ni, Pd, and Pt) phthalocyanines. J Phys Chem C 112 2529-2537... [Pg.214]

Orbitals used in bond formation Nonbonding electron pairs General formula Molecular geometry Molecular shape Bond angle Polarity of molecule Example The name of example compounds... [Pg.37]

The main goal of this chapter is to help you master electron and molecular geometry and hybridization. This will lead to information on the polarity of molecules. You might want to review Section 7-5 on electron configuration. Section 9-7 on writing Lewis structures is also important. Don t Forget —Practice, Practice, Practice. [Pg.146]

In this chapter, we will concentrate on the solid and liquid states. It may be useful to review the section in Chapter 10 that deals with the polarity of molecules. And again, Practice, Practice, Practice. [Pg.158]

Figure 1.10 Polarization of molecules in an electric field. In the absence of an applied electrical field (a), molecules are aligned randomly, with no net dipole. When the field is applied (b), the solvent molecules are polarized and align themselves to reduce the strength of the field... Figure 1.10 Polarization of molecules in an electric field. In the absence of an applied electrical field (a), molecules are aligned randomly, with no net dipole. When the field is applied (b), the solvent molecules are polarized and align themselves to reduce the strength of the field...
Polarization of molecule A in the field of molecule B, or vice versa. These two contributions are summed up as the polarization energy AEpol-... [Pg.20]

In this section, you have pieced together the main components that determine the structure and polarity of molecules. Why is the polarity of a molecule important Polar molecules attract one another more than nonpolar molecules do. Because of this attraction, many physical properties of substances are affected hy the polarity of their molecules. In the next section, you will consider some of these physical properties for liquid and solid substances, and learn about other forces that have a significant effect on the interactions within and among molecules. [Pg.189]

O O Identify and explain the factors that determine the structure and polarity of molecules. [Pg.189]

Strength of the dispersion force(s) depends on how readily electrons can be polarized. 1 point for mentioning the concept of polarization of molecules and its effect on BP. [Pg.67]

The solubility of molecules can be explained on the basis of the polarity of molecules. Polar, e.g. water, and nonpolar, e.g. benzene, solvents do not mix. In general, like dissolves like i.e., materials with similar polarity are soluble in each other. A polar solvent, e.g. water, has partial charges that can interact with the partial charges on a polar compound, e.g. sodium chloride (NaCl). As nonpolar compounds have no net charge, polar solvents are not attracted to them. Alkanes are nonpolar molecules, and are insoluble in polar solvent, e.g. water, and soluble in nonpolar solvent, e.g. petroleum ether. The hydrogen bonding and other nonbonding interactions between molecules are described in Chapter 2. [Pg.5]

R. Schinke Photodissociation Dynamics 2. L. Frommhold Collision-Induced Absorption in Gases 3. T. F. Gallacher Rydberg Atoms 4. M. Auzinsh and R. Ferber Optical Polarization of Molecules 5.1. E. McCarthy and E. Weigold Electron-Atom Collisions 6. V. Schmidt Electron Spectrometry of Atoms using Synchrotron Radiation 7. Z. Rudzikas Theoretical Atomic Spectroscopy... [Pg.428]

Y1U Carlos Furio and Ma. Luisa vJ Calatayud, "Difficulties with the Geometry and Polarity of Molecules Beyond Misconceptions," /. Chem. Educ., Vol. 73,1996,36-41. [Pg.383]

In this paper it has been attempted to provide an introductory overview of some of the various nonlinear optical characterization techniques that chemists are likely to encounter in studies of bulk materials and molecular structure-property relationships. It has also been attempted to provide a relatively more detailed coverage on one topic to provide some insight into the connection between the macroscopic quantities measured and the nonlinear polarization of molecules. It is hoped that chemists will find this tutorial useful in their efforts to conduct fruitful research on nonlinear optical materials. [Pg.93]

The formation of a 1 1 complex between open form of 16a-c and Mg21 leads to an increase in the rate constant for the dark ring-closure reaction of 16a-c (Scheme 20, Table 3). The Mg2+ ion binds with carbonyl oxygen atom what leads to the increase of the polarity of molecule (Scheme 20). In the polar form the dark ring-closure reaction occurs more easily. [Pg.248]

Owing to the coincidence between a number of coefficients, the symmetry of the equations obtained is considerably higher, as compared to (5.22) and (5.23). In addition, the terms responsible for the dynamic Stark effect disappear, which agrees perfectly with the analysis performed in the preceding section concerning the influence of the dynamic Stark effect on optical polarization of molecules. [Pg.196]

Thus, the polarization aspects of such a wide class of photoprocesses, as discussed in the present section, namely photodissociation and photoionization, make it possible to obtain information both on the stereodynamics of the process and on the properties (for instance, symmetry types) of the states through which the transition takes place. It ought to be mentioned that photodissociation can be considered not only as a reaction of a photon with a molecule, but as a halfcollision , in which only the second stage of a collision is present, namely the departure of the products without their previous approach. In the following section we will dwell on the polarization of molecules in full collision, both reactive and non-reactive. [Pg.221]

So far we have considered various radiational and collisional mechanisms of polarization of molecules. There exist earlier methods applying the action of an external stationary magnetic, later of an external electrostatic, field to beam molecules for producing anisotropic distribution of the angular momentum J and of the molecular axis. [Pg.231]

Optical polarization of molecules / Marcis Auzinsh, Ruvin Ferber. [Pg.312]

We are especially grateful to R.N. Zare, the author of pioneer ideas and research in polarization of molecules for his valuable comments and suggestions. [Pg.321]


See other pages where Polarity, of molecules is mentioned: [Pg.423]    [Pg.164]    [Pg.182]    [Pg.183]    [Pg.234]    [Pg.863]    [Pg.51]    [Pg.447]    [Pg.166]    [Pg.476]    [Pg.17]    [Pg.114]    [Pg.173]    [Pg.178]    [Pg.101]    [Pg.457]    [Pg.397]    [Pg.435]    [Pg.422]    [Pg.88]    [Pg.309]    [Pg.310]    [Pg.311]   
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See also in sourсe #XX -- [ Pg.22 , Pg.23 , Pg.24 ]

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