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Single bond, energies

Stereochemistry. Cyclohexane can exist ia two molecular conformations the chair and boat forms. Conversion from one conformation to the other iavolves rotations about carbon—carbon single bonds. Energy barriers associated with this type of rotation are low and transition from one form to the other is rapid. The predominant stereochemistry of cyclohexane has no influence ia its use as a raw material for nylon manufacture or as a solvent. [Pg.407]

C06-0059. Consult Table to find the single-bond energies for bonds between identical row 3 elements (for example, P—P). Is there a trend If so, use the trend to predict the bond energy of an A1—A1 bond. [Pg.422]

Calculated values are derived from data at 298 K. The experimental values are DJ figures. F indicates use of the fully weakened covalent single bond energy, F " the unweakened bond energy. [Pg.34]

The mean bond energy Z (S—F) for SF6 can be regarded as a single bond energy and its transferability to ternary compounds can be examined in S—N—F compounds (see Table XX). [Pg.49]

In the light of several allotropic modifications known for phosphorus, the relatively high single bond energies and the tendency of phosphorus to catenate it remains mysterious, and that apart from P4 and As4 only very scarce information on isolated E cluster molecules is available from hard experimental data. In contrast, a vast amount of solid theoretical work has been performed [11],... [Pg.211]

Table 2.1 lists a few typical single-bond energies for homoatomic (A—A or B—B) and heteroatomic (A—B) bonds. [Pg.31]

What do the following mean single bond energies tell us about the susceptibility of fluorocarbons to hydrolysis ... [Pg.234]

Values for single-bond energies, defined in this way, for many bonds can be found by this process—for the S—S bond from the Sg molecule (an eight-membered ring containing eight S—S bonds), for N—H, P—H, S—H, and so forth from NH, PHS, H S, and so forth. These values are given m Table 3-4. [Pg.84]

Figl 3-6.—The values of single-bond energies of elements. [Pg.88]

TABLE 9 HOMQATOM1C SINGLE BOND ENERGIES (KCAL/MOLE)... [Pg.343]

TABLE 10 REPRESENTATIVE SINGLE-BOND ENERGIES (In kcal/mole)... [Pg.343]

According to the theoretical analysis of this model24,25), even with the single bond energy which only little exceeds that of the thermal motion, in practice an oligomer exists in equilibrium only in two states — free and completely bound, i.e., the interaction scheme being... [Pg.145]

The 1Pi mercury atoms which possess nearly 155 kcal.mole-1 of energy are capable of initiating many chemical reactions. Nearly all single bond energies... [Pg.7]

For the purposes of an engineering design at an early stage, the reaction enthalpy may be needed to an accuracy of only, say, 8 kcal/mol. Without resorting to a single bond energy table, one can predict that this reaction will be close to thermoneutral because the bonds broken and formed are so similar ... [Pg.191]


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See also in sourсe #XX -- [ Pg.83 ]




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