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Lewis structures construction

Let s construct the Lewis structure for the simplest organic molecule, the hydrocarbon methane, CH4. First, we count the valence electrons available from all the atoms in the molecule. For methane, the Lewis symbols of the atoms are... [Pg.190]

The general procedure for constructing the Lewis structure of any molecule or ion is set out in Toolbox 2.1 at the end of this section, but the following information is essential for applying those rules. [Pg.190]

Use the four-step procedure described earlier. Begin with the Lewis structure for the molecule, and then identify the appropriate hybrid orbitals. Construct a a bond framework, and complete the bonding picture by assembling the bonds from the unhybridized p orbitals. [Pg.690]

To learn how to construct Lewis structures for molecules let s examine the following rules by applying them to the CCI4 molecule ... [Pg.10]

STRATEGY Draw the Lewis structure and determine the electron arrangement about the central atom. The number of orbitals required for the electron arrangement determines the hybridization scheme used, as shown in Table 3.2. Construct the hybrid orbitals from atomic orbitals, using the same number of atomic orbitals as hybrid orbitals. Start with the s-orbital, then add p- and d-orbitals as needed. [Pg.265]

The ethylene molecule will illustrate construction of a model containing both a and 77 bonding. The Lewis structure (22) shows that each carbon should be approximately trigonal. Therefore we need sp2 hybrids on each carbon. Figure... [Pg.25]

Many binary Sn(IV) compounds are known. Sn02 has the rutile structure, and SnX2 with X = S, Se, Te the Cdl2 layer structure. SnF4 has a layer structure constructed from corner-sharing octahedra, but other tetrahalides form tetrahedral molecules. The halides are good Lewis acids, especially SnF4, which forms... [Pg.76]

Figure 1.9 illustrates the construction of a Lewis structure for a more complex example, nitromethane. In this case there are a number of reasonable (according to what we know now) constitutional isomers. Therefore, we must be told the connectivity, or which atoms are bonded to which. Once the connectivity shown in Figure 1.9 is given, the best structure that satisfies the octet rule has some formal charges. This still represents a quite stable molecule. [Pg.14]

In order to fully appreciate and understand molecular structure, you will need to be able to construct representations of various molecules. One of the easiest ways to do this is using Lewis structures. The procedure is a bit more complicated than for ionic compounds because of the increasing complexity of covalent compounds. The basic procedure for constructing Lewis diagrams of molecules consists of 4 steps ... [Pg.117]

When constructing molecular models, it helps to review the Lewis structures for the molecule. If you recall from Chapter 6, Lewis structures display two... [Pg.127]

To see how these rules are applied, we will construct the Lewis structures for a few molecules. We will first consider the water molecule and follow the rules above. [Pg.613]

The ability to construct Lewis structures is fundamental to writing or understanding organic reaction mechanisms. It is particularly important because lone pairs of electrons frequently are crucial to the mechanism but often are omitted from structures appearing in the chemical literature. [Pg.2]

This process of constructing functions for the various resonant formulae, followed by an adequate combination of them, is mathematically more complex than the mathematics of molecular orbital theory. It is therefore understandable that, after the initial preference of chemists for the v.b. bond theory which has a closer relation to Lewis structures - especially due to the contribution of Linus Pauling - m.o. theory became increasingly popular. In addition, m.o. theory leads directly, not only to fundamental states (through the occupied m.o.), but also to excited states (through vacant m.o.) of molecules. In recent years, however, a new form of valence-bond theory has been developed that is more amenable to computation (spin-coupled valence-bond theory) in which the molecular wavefunction is expressed as a linear combination of all the coupling schemes of the various electrons corresponding to the same resultant spin (ref. 97). [Pg.183]

Perhaps the most constructive contribution to solve this problem is the study of pair-densities in hydrides of elements from lithium to fluorine by Bader and Stephens 116). One major advantage is that it is not a predetermined working hypothesis, but a quantitative test of validity of Lewis structures, which may be appropriate or not. Bader and Stephens conclude that spatially localized pairs are satisfactory in LiH, BeH2, BH3 and BHT that CH4 (among all molecules) is a border-line case, and that intra-correlated pair-functions would fail to recover a major fraction of the correlation energy in NH3, H20 and HF. It is also true for the neon atom and for N2 and F2 that most of the correlation energy comes from correlation between even the best optimized electron-pairs. There is no physical basis for the view that there are two separately localized pairs of non-bonded electrons in HzO. [Pg.26]

Fig. 1 Lewis structure of the [C2mim]+ cation in order to illustrate the applied labeling of the imi-dazolium ring. The H2 hydrogen atom is bonded to the C2 carbon atom of the ring. Note that this structure is constructed after the suggestion for the [C4mim]+ cation of Hunt et al. [30]... Fig. 1 Lewis structure of the [C2mim]+ cation in order to illustrate the applied labeling of the imi-dazolium ring. The H2 hydrogen atom is bonded to the C2 carbon atom of the ring. Note that this structure is constructed after the suggestion for the [C4mim]+ cation of Hunt et al. [30]...
Magnus, P., Lewis, R., and Bennett, E, Synthetic and mechanistic studies on the antitumor antibiotics esperamicin A and caUcheamicin Oxidative functionalization of the 13-ketobicy-clo[7.3.1]tridecenediyne core structure. Construction of the aHylic trisulfide trigger, 7. Am. Chem. Soc., 114, 2560, 1992. [Pg.323]

This text describes two ways to construct Lewis structures from chemical formulas. In this chapter, you will find that Lewis structures for many common substances can be drawn by giving each type of atom its most common number of covalent bonds and lone pairs. You will learn a more widely applicable procedure for drawing Lewis structures in Chapter 12. [Pg.83]

Total the valence electrons and construct the Lewis structures for (a) NH3 and (b) F2CO. Answer ... [Pg.277]


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See also in sourсe #XX -- [ Pg.14 , Pg.16 , Pg.17 , Pg.18 , Pg.19 , Pg.20 , Pg.21 ]




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