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Hybrid forms

The O atom uses one of its sp or sp hybrids to form the CO a bond and antibond. When sp hybrids are used in conceptualizing the bonding, the other sp hybrid forms a lone pair orbital directed away from the CO bond axis one of the atomic p orbitals is involved in the CO n and 71 orbitals, while the other forms an in-plane non-bonding orbital. Alternatively, when sp hybrids are used, the two sp hybrids that do not interact with the C-atom sp2 orbital form the two non-bonding orbitals. Hence, the final picture of bonding, non-bonding, and antibonding orbitals does not depend on which hybrids one uses as intermediates. [Pg.164]

Those propylene species that the authors were using are no different than safrole or aiiyibenzene. In fact, safrole is a perfect substitute. Yowza Those recipes look awesome Now as Strike understands it, there has already been a detailed writeup of the by-the-numbers application of the above patent as written. This, Strike beiieves, can be found in Uncle Fester s Secrets of LSD Manufacture and/or Secrets of Methamphetamine Manufac-ture [18]. But our adventurous chemist Suniight came thru again and submitted a new, hybrid form of this method which she seems to have formulated after a lot of thought on the matter. So here again is Suniight ... [Pg.83]

Given the information in Exercise 3.47, plot a graph showing how the hybridization depends on the angle between two hybrids formed from an s-orbital and two p-orbitals, and confirm that it ranges from 90° when no s-orbital is included in the mixture to 120° when the hybridization is sp2. [Pg.254]

Two other, closely related, consequences flow from our central proposition. If the d orbitals are little mixed into the bonding orbitals, then, by the same token, the bond orbitals are little mixed into the d. The d electrons are to be seen as being housed in an essentially discrete - we say uncoupled - subset of d orbitals. We shall see in Chapter 4 how this correlates directly with the weakness of the spectral d-d bands. It also follows that, regardless of coordination number or geometry, the separation of the d electrons implies that the configuration is a significant property of Werner-type complexes. Contrast this emphasis on the d" configuration in transition-metal chemistry to the usual position adopted in, say, carbon chemistry where sp, sp and sp hybrids form more useful bases. Put another way, while the 2s... [Pg.25]

FACTORS AFFECTING THE TYPE OF ORGANOCLAY HYBRID FORMED... [Pg.31]

Operations Op can be seen as operators that can take on a logical integer, analytic (static or dynamic), or hybrid form. With each operation we have associated an integer-valued variable, aj t), which determines the discrete state that the operator takes on with time. [Pg.41]

Nineham1 proposed that tetrazolium salts exist as resonance hybrids forms (120) and (121) (shown for 2,3-substituted ones). However, UV-... [Pg.238]

The orbitals containing the bonding electrons are hybrids formed by the addition of the wave functions of the s-, p-, d-, and f- types (the additions are subject to the normalization and orthogonalization conditions). Formation of the hybrid orbitals occurs in selected symmetric directions and causes the hybrids to extend like arms on the otherwise spherical atoms. These arms overlap with similar arms on other atoms. The greater the overlap, the stronger the bonds (Pauling, 1963). [Pg.67]

From the sketch, we can see that two p orbitals and one s orbital are being hybridized, forming three new sp2 hybrid orbitals. See the following figure in Section 8-6. The three sp2 hybrid orbitals are arranged as so ... [Pg.118]

If the product ratios indicate the contribution of hybrid forms 5a and 5b, 62% of radicals 5 exist in the 5a form. [Pg.331]

Still another aspect of the Li and F valence orbitals is modified by ionic-bond formation. In an isolated ionic or neutral species, each NAO retains the characteristic angular shape of the pure s and p hydrogenic orbitals shown in Fig. 1.1, reflecting the full rotational symmetry of atoms. However, in the presence of another atom or ion this symmetry is broken, and the optimal valence orbitals acquire sp hybrid form (assumed for simplicity to include only valence s and p orbitals), as represented mathematically by... [Pg.52]

Sigma- and pi-type donor acceptor interactions Further details of the leading hp —hM donor-acceptor interactions are gathered in Table 2.5 and Figure 2.21. For each such interaction the table shows the hybrid form of the donor (hp)23 and acceptor (hM) orbitals, the occupancy of the acceptor, and the second-order estimate (cf. Eq. (1.35) or (2.7)) of the donor-acceptor stabilization energy. Let us now discuss some of the trends displayed in Table 2.5. [Pg.82]

We can also verify that the usual ECAO-MO description (3.2) and (3.4) leads to predicted hybridizations that are generally consistent with the donor-acceptor estimates (3.8). Suppose that each H atom is associated with a valence spin-orbital of hybridized form (3.6). According to Eq. (3.2), the optimal electronic energy of bond formation is obtained by choosing the hybridization parameter k to maximize the magnitude of the interaction element... [Pg.95]

Figure 8.10 The quaternary structure of proteins. The enzyme lactate dehydrogenase (EC 1.1.1.27) has a relative molecular mass of approximately 140 000 and occurs as a tetramer produced by the association of two different globular proteins (A and B), a characteristic that results in five different hybrid forms of the active enzyme. The A and B peptides are enzymically inactive and are often indicated by M (muscle) and H (heart). The A4 tetramer predominates in skeletal muscle while the B4 form predominates in heart muscle but all tissues show most types in varying amounts. Figure 8.10 The quaternary structure of proteins. The enzyme lactate dehydrogenase (EC 1.1.1.27) has a relative molecular mass of approximately 140 000 and occurs as a tetramer produced by the association of two different globular proteins (A and B), a characteristic that results in five different hybrid forms of the active enzyme. The A and B peptides are enzymically inactive and are often indicated by M (muscle) and H (heart). The A4 tetramer predominates in skeletal muscle while the B4 form predominates in heart muscle but all tissues show most types in varying amounts.
If a single-stranded DNA molecule is placed with a complementary single DNA sequence the two molecules will hybridize. This hybridization forms the basis of a number of very powerful techniques for detecting and quantifying specific nucleic acid sequences. The hybridization may be carried out either in solution or more commonly with the DNA immobilized on nitrocellulose filters. The complementary DNA sequence is known as a cDNA probe. Probes for a large number of important nucleic acid sequences are now available. [Pg.461]

Koshland s model also assumes two states, R and T, but of each subunit. The binding of one ligand causes only one subunit to switch completely but induces a slight change in a neighbouring subunit which can now bind another ligand molecule easily. Because each subunit changes in turn, hybrid forms of R and T conformations are possible. [Pg.61]

This process has many benefits in the context of green chemistry it involves two enzymatic steps, in a one-pot procedure, in water as solvent at ambient temperature. It has one shortcoming, however-penicillin acylase generally works well only with amines containing an aromatic moiety and poor enantioselectivities are often observed with simple aliphatic amines. Hence, for the easy-on/easy-off resolution of aliphatic amines a hybrid form was developed in which a hpase [Candida antarctica hpase B (CALB)] was used for the acylation step and peniciUin acylase for the deacylahon step [22]. The structure of the acyl donor was also optimized to combine a high enanhoselectivity in the first step with facile deacylation in the second step. It was found that pyridyl-3-acetic acid esters gave optimum results (see Scheme 6.8). [Pg.116]

Thus we have argued that the only hybrid form which is correct for the slowly-varying densities is that of Eq. (36), with a value of a between 0 and 0.2. Note that the approximation a = 1, which reproduces exact exchange, ignores the cancellation of nonlocalities between the exchange and correlation energies, and the fourth column of Table 3 shows how poor the latter approximation is. [Pg.23]

Fig. 7.17 Successive transformations of linear combinations of atomic orbitals, beginning with atomic s and p orbitals, proceeding to sp3 hybrids, forming bond orbitals and antibond orbitals, then coupling to form the valence band and conduction band respectively. (After Harrison (1980).). Fig. 7.17 Successive transformations of linear combinations of atomic orbitals, beginning with atomic s and p orbitals, proceeding to sp3 hybrids, forming bond orbitals and antibond orbitals, then coupling to form the valence band and conduction band respectively. (After Harrison (1980).).
FIGURE 8-32 DNA hybridization. Two DNA samples to be compared are completely denatured by heating. When the two solutions are mixed and slowly cooled, DNA strands of each sample associate with their normal complementary partner and anneal to form duplexes. If the two DNAs have significant sequence similarity, they also tend to form partial duplexes or hybrids with each other the greater the sequence similarity between the two DNAs, the greater the number of hybrids formed. Hybrid formation can be measured in several ways. One of the DNAs is usually labeled with a radioactive isotope to simplify the measurements... [Pg.293]

In molecules which are known to have a trigonal bipyramid structure, energy criteria make it unlikely that the first four combinations are important. In PF combination (5) is the most probable and the hybrids are labelled dsp1. In gaseous MoCl it is likely that a combination of (5) and (6) are used, since the 4d and 5p AOa of Mo are close in energy. The hybrid formed from the orbitals in (6) is labelled d sp and the most general form for in MoCl is... [Pg.229]


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Factors Affecting the Type of Organoclay Hybrid Formed

Hybrid Structures Formed by Lead 1,3-Cyclohexanedicarboxylates

Hybrid fiber forming processes

Hybrid reduced form model

Nonallelic Genes Controlling the Synthesis of Isozymes Which Form Hybrid Patterns

Quaternion form of the hybrid orbitals and hybridization tetrahedra

The mathematical form of hybrid orbitals

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