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Bond diatomic compounds

In compounds, mercury has the oxidation number +1 or +2. Its compounds with oxidation number +1 are unusual in that the mercury(I) cation is the covalently bonded diatomic ion (Hg—Hg)2+, written Hg22+. [Pg.788]

Figure 4.10 Calculated relativistic bond contractions ARte in A (circles and solid line, axis on the left-hand side) and relativistic change in the dissociation energy contractions (triangles and dashed line, axis on the right-hand side) for various diatomic compounds as a function ofthe electronegativity of the ligand. Figure 4.10 Calculated relativistic bond contractions ARte in A (circles and solid line, axis on the left-hand side) and relativistic change in the dissociation energy contractions (triangles and dashed line, axis on the right-hand side) for various diatomic compounds as a function ofthe electronegativity of the ligand.
The diatomic compounds often add to ethylenic double bonds and may react with the heavier alkali and alkaline earth metals to give polyhalide salts. [Pg.576]

The critical parameter is the bond length across which the a- o transition occurs, as Is illustrated by the simple diatomic compounds... [Pg.134]

A diatomic compound is one that is composed of two atoms joined by a covalent bond. [Pg.85]

Covalent bonds between atoms of the same elements are known as non-polar covalent bonds. You can think of them as identical twin bonds. These bonds in the same family share electrons and are found in diatomic compounds such as H2 and I2. Non-polar bonds allow atoms to be more stable together than they are by themselves. [Pg.183]

Although all covalent bonds involve the sharing of electrons, they differ widely in the degree of sharing. Homonuclear diatomics such as Hj, Nj, Oy and F2 share the electrons equally between the two atoms and are said to have nonpolar covalent bonds. Many compounds such as HCl and H2O share the electrons in the bond unequally and are said to contain polar covalent bonds. The polarity in the bond increases with increasing difference in electronegativity between the bonded atoms (Table 1.6). [Pg.42]

All six of the possible diatomic compounds between F, Cl, Br, and I are known (Table VI) and, except for BrF and IF, which are too unstable with respect to disproportionation to permit isolation at room temperature, they can be prepared by direct combination of the elements X2 and Y2. The properties of the compounds tend to be intermediate between those of the pure, parent halogens. Most add to carbon-carbon double bonds (Section IX. C), and some are useful as nonaqueous solvents. Liquid ICl, in particular, dissolves the chlorides of Group lA to give highly conducting solutions. [Pg.131]

As in the case of ions we can assign values to covalent bond lengths and covalent bond radii. Interatomic distances can be measured by, for example. X-ray and electron diffraction methods. By halving the interatomic distances obtained for diatomic elements, covalent bond radii can be obtained. Other covalent bond radii can be determined by measurements of bond lengths in other covalently bonded compounds. By this method, tables of multiple as well as single covalent bond radii can be determined. A number of single covalent bond radii in nm are at the top of the next page. [Pg.48]

A more useful quantity for comparison with experiment is the heat of formation, which is defined as the enthalpy change when one mole of a compound is formed from its constituent elements in their standard states. The heat of formation can thus be calculated by subtracting the heats of atomisation of the elements and the atomic ionisation energies from the total energy. Unfortunately, ab initio calculations that do not include electron correlation (which we will discuss in Chapter 3) provide uniformly poor estimates of heats of formation w ith errors in bond dissociation energies of 25-40 kcal/mol, even at the Hartree-Fock limit for diatomic molecules. [Pg.105]

Aii vaiues (other than those for diatomic molecules) are averages over different compounds. A bond in any given compound may have a vaiue that differs from the average by between 5 and 20 kJ/mol. [Pg.380]

Figure 4.9 Experimental bond distances for selected diatomic Croup 11 compounds (data are from Refs. [34, 159]). Figure 4.9 Experimental bond distances for selected diatomic Croup 11 compounds (data are from Refs. [34, 159]).
Figure 5.2 Correlation of the hardnesses of the Group IV elements, and the associated isoelectronic III-V compounds, with their bond moduli. Room temperature data. For the elements, the molecular volumes refer to the diatoms C-C, Si-Si, Ge-Ge, and Sn-Sn. Figure 5.2 Correlation of the hardnesses of the Group IV elements, and the associated isoelectronic III-V compounds, with their bond moduli. Room temperature data. For the elements, the molecular volumes refer to the diatoms C-C, Si-Si, Ge-Ge, and Sn-Sn.

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See also in sourсe #XX -- [ Pg.199 ]




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Diatomic compounds

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