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Bond dissociation energy hydrogen molecule

Resonance theory can also account for the stability of the allyl radical. For example, to form an ethylene radical from ethylene requites a bond dissociation energy of 410 kj/mol (98 kcal/mol), whereas the bond dissociation energy to form an allyl radical from propylene requites 368 kj/mol (88 kcal/mol). This difference results entirely from resonance stabilization. The electron spin resonance spectmm of the allyl radical shows three, not four, types of hydrogen signals. The infrared spectmm shows one type, not two, of carbon—carbon bonds. These data imply the existence, at least on the time scale probed, of a symmetric molecule. The two equivalent resonance stmctures for the allyl radical are as follows ... [Pg.124]

The species H2 and H3+ are important as model systems for chemical bonding theory. The hydrogen molecule ion H2+ comprises 2 protons and 1 electron and is extremely unstable even in a low-pressure gas discharge system the energy of dissociation and the intemuclear distance (with the corresponding values for H2 in parentheses) are ... [Pg.37]

FIGURE 2.18 The bond dissociation energies of the hydrogen halide molecules in kilojoules per mole of molecules. Note how the bonds weaken as the halogen atom becomes larger. [Pg.206]

Formula H2O MW 18.015 bent molecule H-O-H bond angle 104.5° H-0 bond distance 0.9575 A bond dissociation energy of 0-H bond 101.2 kcal/mol intermolecular force hydrogen bonding... [Pg.967]

During coal conversion, the coal structure influences both thermal and catalytic reactions. Thermal reactions of solid coals initiate the breakage of weak bonds at rates proportional to their bond dissociation energies. The radicals thus produced require stabilization by hydrogenation or addition of small molecules otherwise the radicals couple to produce much more thermally stable bonds, which eventually leads finally to the formation of infusible and insoluble coke. [Pg.43]

The difference between the O—11 bond-dissociation energies for H20 and Oil can be ascribed to the stabilization energy of the normal state, 3P, of the oxygen atom. When one O—H bond is broken in the water molecule there is produced, in addition to a hydrogen atom, an... [Pg.622]

Fig. 17.12 Bond dissociation energies and bond lengths of the hydrogen halides, methyl halides, and halogen molecules. Note that this figure, which is taken directly from Politzcr s work, portrays in a different way relationships that are closely rebled to Fig. 9.7. (From Politzer. P. J. Am. Chetn. See. 1969. 91.6235. Reproduced with permission.)... Fig. 17.12 Bond dissociation energies and bond lengths of the hydrogen halides, methyl halides, and halogen molecules. Note that this figure, which is taken directly from Politzcr s work, portrays in a different way relationships that are closely rebled to Fig. 9.7. (From Politzer. P. J. Am. Chetn. See. 1969. 91.6235. Reproduced with permission.)...
Once produced, a chlorine atom can remove a hydrogen atom from a methane molecule and form a methyl radical and a hydrogen chloride molecule. The bond-dissociation energies of CH4 (104 kcal) and HC1 (103.1 kcal) suggest that this reaction is endothermic by about 1 kcal ... [Pg.93]


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Bond dissociation energy

Bonding molecules

Bonds bond dissociation energies

Dissociation energy, hydrogen molecule

Dissociation hydrogen bonds

Dissociative bond energy

Hydrogen bond dissociation energies

Hydrogen bond energy

Hydrogen bonding bond energies

Hydrogen bonding energies

Hydrogen dissociation

Hydrogen dissociation energy

Hydrogen energy

Hydrogen molecul

Hydrogen molecule

Hydrogen molecule, bonding

Hydrogen molecule, dissociation

Hydrogen-bonded molecules

Hydrogenation energies

Hydrogenative dissociation

Molecules dissociation energy

Molecules energy

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