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Distribution of bond

Some systematic studies on the different reaction schemes and how they are realized in organic reactions were performed some time ago [18]. Reactions used in organic synthesis were analyzed thoroughly in order to identify which reaction schemes occur. The analysis was restricted to reactions that shift electrons in pairs, as either a bonding or a free electron pair. Thus, only polar or heteiolytic and concerted reactions were considered. However, it must be emphasized that the reaction schemes list only the overall change in the distribution of bonds and ftee electron pairs, and make no specific statements on a reaction mechanism. Thus, reactions that proceed mechanistically through homolysis might be included in the overall reaction scheme. [Pg.188]

This study of thermochemical data for a very large number of substances has shown that in every case for which the data are reliable the observed energy of the molecule is equal to that calculated for an assumed distribution of bonds or differs from it in the direction corresponding to greater stability, in accord with the quantum-... [Pg.141]

In this section, we develop a process for making schematic drawings of molecules called Lewis structures. A Lewis structure shows how the atoms in a molecule are bonded together. A Lewis structure also reveals the distribution of bonding and nonbonding valence electrons in a molecule. In a sense, a Lewis structure is a molecular blueprint that... [Pg.582]

Fig. 7.4 Distributions of bond lengths found in the CSD for all single Csp -Csp bonds (closed line), for the methylene analogs RCH2-CH2R (dashed line) and for single bonds between quaternary carbons R3C-CR3 (dotted line). Fig. 7.4 Distributions of bond lengths found in the CSD for all single Csp -Csp bonds (closed line), for the methylene analogs RCH2-CH2R (dashed line) and for single bonds between quaternary carbons R3C-CR3 (dotted line).
All are tertiary halides so that attack by the S mode would not be expected to occur on (16) or (17) any more than it did on (8) (cf. p. 82). Sn2 attack from the back on the carbon atom carrying Br would in any case be prevented in (16) and (17) both sterically by their cagelike structure, and also by the impossibility of forcing their fairly rigid framework through transition states with the required planar distribution of bonds to the bridgehead carbon atom (cf. p. 84). Solvolysis via rate-limiting formation of the ion pair (SN1), as happens with (8) is... [Pg.86]

Fig. 29. Schematic diagram of the influence of hydrogen on the distribution of Si—Si and Si—H bonds during film growth, (a) shows the hydrogen chemical potential intersecting a possible distribution of bonds while (b) illustrates the expected result due to lattice relaxation (Street et al., 1988). Fig. 29. Schematic diagram of the influence of hydrogen on the distribution of Si—Si and Si—H bonds during film growth, (a) shows the hydrogen chemical potential intersecting a possible distribution of bonds while (b) illustrates the expected result due to lattice relaxation (Street et al., 1988).
Homoconjugational interactions and nonbonding intramolecular contacts of the four ji-systems are responsible for the observed distribution of bond angles at the central atom, which are also significantly inequivalent [105.1(1)° to 111.8(1)°]. [Pg.31]

It is well known that one can obtain valuable structural and stereochemical information from ( N-1 ) and study the distribution of bonding electrons. The theory of spin-spin coupling is covered satisfactorily in many books79,80. [Pg.318]

Whereas the majority of reactions of acetic anhydride with wood are thermally assisted, there has been some interest in using other methods for delivering energy. Larsson Brelid (2002), Larsson Brelid and Simonson (1999) and Larsson Brelid etal. (1999) studied the use of microwave heating to acetylate wood in order to reduce reaction times, improve the distribution of bonded reagent within the wood and achieve more efficient removal of process chemicals and by-products. [Pg.50]

Pore-size-dependent conductances are assigned to individual pores and channels. Three possible types of bonds befween pores exist. The corresponding bond conductances—(T), and o X)—can be established straightforwardly. The model was extended toward calculation of the complex impedance of the membrane by assigning capacitances in parallel to conductances to individual pores. The probability distribution of bonds to have conductivify cr b, <7br/ or O, is... [Pg.392]

Although no crystal structures of cyclotriphosph(III)azanes have yet been reported, it is reasonable to assume that the ring will adopt a chair conformation and that the nitrogen atoms will have a planar or near-planar distribution of bonds. This is consistent with the structures of the six-membered ring fragments found in the cage... [Pg.103]

The distribution of bond orientations is most conveniently characterized by a probabibty distribution 4)(u), defined such that... [Pg.81]


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Bond Distribution

Distribution of Atom Types H-bond Donors and Acceptors

Distribution of bond strength

Distributions of formation energies - the weak bond model

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