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Lewis structures valence electrons

The Lewis structures for polyatomic ions are developed in the same way as in the illustrated problems. However, in the case of a positive ion like NH4, there is one less than the total number of valence electrons, and in the case of a negative ion like CO/, there are two more than the total number of valence electrons. Lewis structures of typical polyatomic ions are illustrated by the... [Pg.66]

Lewis structures are drawn to represent molecules and polyatomic ions, showing the arrangement of atoms and the positions of all valence electrons. Lewis structures represent the shared pairs of valence electrons either as two dots, , or as a single dash, —. Any unshared electrons are represented as dots. [Pg.305]

When the distribution of valence electrons in a molecule cannot be represented adequately by a single Lewis structure, the structure can be approximated by a combination of Lewis structures that differ only in the placement of electrons. Lewis structures that differ only in the placement of electrons are called resonance structures. We use resonance structures to show the delocalization of electrons and to help predict the most likely electron distribution in a molecule. [Pg.18]

Both ionic and covalent bonds involve valence electrons, the electrons in the outermost energy level of an atom. In 1920, G. N. Lewis, the American chemist shown in Figure 9, came up with a system to represent the valence electrons of an atom. This system—known as electron-dot diagrams or Lewis structures —uses dots to represent valence electrons. Lewis s system is a valuable model for covalent bonding. However, these diagrams do not show the actual locations of the valence electrons. They are models that help you to keep track of valence electrons. [Pg.217]

The atom is composed of the kernel and the outer atom or shell, which in the case of the neutral atom, contains negative electrons in equal numbers to the excess of positive charges of the kernel. Today we refer to the electrons in the outer shell as valence electrons. Lewis suggested the use of the atomic symbol in boldface to represent the kernel of the atom and that valence electrons should be indicated by dots. Figure 7.1 shows the electronic structures of the second-period elements from Li to F as suggested by Lewis. [Pg.100]

If we use the expanded valence-shell Lewis-structure (33) to represent the electronic structure of FSN, we cannot account for the observed lengthening of the S-F bond relative to that of a single bond. By contrast, the S-F bond-length of 1.55 A for F3SN is essentially that of a single bond, and the expanded valence-shell Lewis structure (27) is in accord with this observation. This structure for F3SN is also able to account for the observed shortening of the S-N bond (1.42 A) relative to those of free SN (1.50 A) and FSN (1.45 A), whose electronic structures are to be described by (28) and resonance between (32) and (33) respectively. [Pg.225]

The presence of unpaired electrons causes odd-electron species to be paramagnetic. NO is paramagnetic. Molecules with an even number of electrons are expected to have all electrons paired and to be diamagnetic. An important exception is seen in the case of O2, which is paramagnetic despite having 12 valence electrons. Lewis theory does not provide a good electronic structure for O2, but the molecular orbital theory that we will consider in the next chapter is much more successful. [Pg.434]

Trivalent ( classical carbenium ions contain an sp -hybridized electron-deficient carbon atom, which tends to be planar in the absence of constraining skeletal rigidity or steric interference. The carbenium carbon contains six valence electrons thus it is highly electron deficient. The structure of trivalent carbocations can always be adequately described by using only two-electron two-center bonds (Lewis valence bond structures). CH3 is the parent for trivalent ions. [Pg.147]

The structure shown is the best (most stable) Lewis structure for methyl nitrite All atoms except hydro gen have eight electrons (shared + unshared) in their valence shell... [Pg.20]

When writing a Lewis structure we restrict a molecule s electrons to certain well defined locations either linking two atoms by a covalent bond or as unshared electrons on a sm gle atom Sometimes more than one Lewis structure can be written for a molecule espe cially those that contain multiple bonds An example often cited m introductory chem istry courses is ozone (O3) Ozone occurs naturally m large quantities m the upper atmosphere where it screens the surface of the earth from much of the sun s ultraviolet rays Were it not for this ozone layer most forms of surface life on earth would be dam aged or even destroyed by the rays of the sun The following Lewis structure for ozone satisfies fhe ocfef rule all fhree oxygens have eighf elecfrons m fheir valence shell... [Pg.24]

Lewis structures in which second row elements own or share more than eight valence electrons are especially unstable and make no contribution to the true structure (The octet rule may be ex ceeded for elements beyond the second row)... [Pg.26]

Section 1 3 The most common kind of bonding involving carbon is covalent bond ing A covalent bond is the sharing of a pair of electrons between two atoms Lewis structures are written on the basis of the octet rule, which limits second row elements to no more than eight electrons m their valence shells In most of its compounds carbon has four bonds... [Pg.47]

Based on its structure and valence electron count, draw a Lewis structure or series of Lewis structures for diborane Examine the bond density surface. Does it substantiate 01 refute your speculation ... [Pg.44]

Examine electrostatic potential maps for potassium hydride and hydrogen chloride. How are they similar and how are they different (Focus on whether the molecules are polar or nonpolar (compare dipole moments), and on the electronic character of hydrogen.) Draw the ionic Lewis structure that is most consistent with each electrostatic potential map. Does each atom have a filled valence shell ... [Pg.123]

Lewis structure (Section 1.5) A representation of a molecule showing valence electrons as dots. [Pg.1245]

These structures (without the circles) are referred to as Lewis structures. In writing Lewis structures, only the valence electrons written above are shown, because they are the ones that participate in covalent bonding. For the main-group elements, the only ones dealt with here, the number of valence electrons is equal to the last digit of the group number in the periodic table (Table 7.1). Notice that elements in a given main group all have the same number of valence electrons. This explains why such elements behave similarly when they react to form covalently bonded species. [Pg.167]

In the Lewis structure of a molecule or polyatomic ion, valence electrons ordinarily occur in pairs. There are two kinds of electron pairs. [Pg.167]

There are several ways to choose the more plausible of two structures differing in their arrangement of atoms. As pointed out in Example 7.1, the fact that carbon almost always forms four bonds leads to the correct structure for ethane. Another approach involves a concept called formal charge, which can be applied to any atom within a Lewis structure. The formal charge is the difference between the number of valence electrons in the free atom and the number assigned to that atom in the Lewis structure. The assigned electrons include—... [Pg.171]

The largest class of molecules to violate the octet rule consists of species in which the central atom is surrounded by more than four pairs of valence electrons. Typical molecules of this type are phosphorus pentachloride, PC15, and sulfur hexafluoride, SF6. The Lewis structures of these molecules are... [Pg.173]

In 1923. Lewis published a classic book (later reprinted by Dover Publications) titled Valence and the Structure of Atoms and Molecules. Here, in Lewis s characteristically lucid style, we find many of the basic principles of covalent bonding discussed in this chapter. Included are electron-dot structures, the octet rule, and the concept of electronegativity. Here too is the Lewis definition of acids and bases (Chapter 15). That same year, Lewis published with Merle Randall a text called Thermodynamics and the Free Energy of Chemical Substances. Today, a revised edition of that text is still used in graduate courses in chemistry. [Pg.174]

Consider the dichromate ion. It has no metal-metal nor oxygen-oxygen bonds. Write a Lewis structure for die dichromate ion. Consider chromium to have six valence electrons. [Pg.194]

In Chapter 7, we used valence bond theory to explain bonding in molecules. It accounts, at least qualitatively, for the stability of the covalent bond in terms of the overlap of atomic orbitals. By invoking hybridization, valence bond theory can account for the molecular geometries predicted by electron-pair repulsion. Where Lewis structures are inadequate, as in S02, the concept of resonance allows us to explain the observed properties. [Pg.650]

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]

To check on the validity of a Lewis structure, verify that each atom has an octet or a duplet. As we shall see in Section 2.10, a common exception to this rule arises when the central atom is an atom of an element in Period 3 or higher. Such an atom can accommodate more than eight electrons in its valence shell. Consequently, the most stable Lewis structure may be one in which the central atom has more than eight electrons. [Pg.191]

The Lewis structure of a polyatomic species is obtained by using all the valence electrons to complete the octets (or duplets) of the atoms present by forming single or multiple bonds and leaving some electrons as lone pairs. [Pg.193]

Different Lewis structures do not in general make the same contribution to a resonance structure. It is possible to decide which structures are likely to make the major contribution by comparing the number of valence electrons distributed around each atom in a structure with the number of valence electrons on each of the free atoms. The smaller these differences for a structure, the greater is its contribution to a resonance hybrid. [Pg.195]

To assign a formal charge, we establish the ownership of the valence electrons of an atom in a molecule and compare that ownership with the free atom. An atom owns one electron of each bonding pair attached to it and owns its lone pairs completely. The most plausible Lewis structure will be the one in which the formal charges of the atoms are closest to zero. [Pg.196]


See other pages where Lewis structures valence electrons is mentioned: [Pg.40]    [Pg.233]    [Pg.40]    [Pg.233]    [Pg.11]    [Pg.155]    [Pg.18]    [Pg.19]    [Pg.9]    [Pg.18]    [Pg.19]    [Pg.24]    [Pg.1170]    [Pg.42]    [Pg.9]    [Pg.165]    [Pg.190]    [Pg.191]    [Pg.195]    [Pg.199]   
See also in sourсe #XX -- [ Pg.611 , Pg.612 , Pg.613 , Pg.614 ]




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