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Hydrogen molecule covalent bond

Key words Covalent bond - Hydrogen molecule -Helium atom - Noncrossing rule... [Pg.19]

Hydrogen-bonding has a huge influence on the physical properties of molecules. Boiling is the conversion of a liquid (where the molecules are free to move, but linked by intermolecular bonds) to a gas, where (in an ideal gas) the molecules are so distant from each other that they do not interact. Boiling, therefore, does not break the strong covalent bonds within molecules, but rather the weaker intermolecular bonds between them. [Pg.259]

The selection of the solvent is based on the retention mechanism. The retention of analytes on stationary phase material is based on the physicochemical interactions. The molecular interactions in thin-layer chromatography have been extensively discussed, and are related to the solubility of solutes in the solvent. The solubility is explained as the sum of the London dispersion (van der Waals force for non-polar molecules), repulsion, Coulombic forces (compounds form a complex by ion-ion interaction, e.g. ionic crystals dissolve in solvents with a strong conductivity), dipole-dipole interactions, inductive effects, charge-transfer interactions, covalent bonding, hydrogen bonding, and ion-dipole interactions. The steric effect should be included in the above interactions in liquid chromatographic separation. [Pg.89]

Most toxicity is due to the interaction between the ultimate toxicant and a target molecule via covalent bonding non-covalent bonding, hydrogen abstraction, electron transfer, or an enzyme reaction. [Pg.283]

Table 11.1.2. Molecules containing covalently bonded hydrogen... Table 11.1.2. Molecules containing covalently bonded hydrogen...
Hydrogen bonds" are not due to a separate potential they involve the attraction between an H atom that is covalently bonded to molecule 1 and electronegative atoms (O, N, etc.) in molecule 2 that are between 0.15 nm and 0.25 nm from the H atom. This hydrogen bond interaction is a combination of Keesom, Debye, and London interactions. [Pg.196]

Polar covalent bonds are the source of dipoles. Dipole-dipole attractions, including those resulting from hydrogen bonds, hold together liquids composed of polar covalent molecules. But what about molecules with pure covalent bonds Such molecules have no permanent dipoles. So, what intermolecular force holds them together ... [Pg.97]

Formation of a covalent bond Hydrogen (H2), nitrogen (N2), oxygen (O2), fluorine (F2), chlorine (Cy, bromine (Br2), and iodine (I2) occur in nature as diatomic molecules, not as single atoms because the molecules formed are more stable than the indiviual atoms. How do two atoms that do not give up electrons bond with each other ... [Pg.242]

The Lewis model for covalent bonding starts with the recognition that electrons are not transferred from one atom to another in a nonionic compound, but rather are shared between atoms to form covalent bonds. Hydrogen and chlorine combine, for example, to form the covalent compound hydrogen chloride. This result can be indicated with a Lewis diagram for the molecule of the product, in which the valence electrons from each atom are redistributed so that one electron from the hydrogen atom and one from the chlorine atom are now shared by the two atoms. The two dots that represent this electron pair are placed between the symbols for the two elements ... [Pg.85]

Intermolecular forces Attractive forces fhat act between molecules weaker than covalent bonds Hydrogen bonding Attraction between a hydrogen atom bonded to a highly electronegative atom (0. N, F) and the lone pair on an electronegative atom in another or the same molecule... [Pg.113]

Hydrocarbons are compounds composed entirely of carbon and hydrogen atoms bonded to each other by covalent bonds. These molecules are further classified as saturated or unsaturated. Saturated hydrocarbons have only single bonds between carbon atoms. These hydrocarbons are classified as alkanes. Unsaturated hydrocarbons contain a double or triple bond between two carbon atoms and include alkenes, alkynes, and aromatic compounds. These classifications are summarized in Figure 19.3. [Pg.469]


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See also in sourсe #XX -- [ Pg.65 , Pg.66 , Pg.73 , Pg.74 , Pg.75 ]

See also in sourсe #XX -- [ Pg.5 ]




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