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Lobes, atomic orbital

Since these new orbitals are a mixture of the two original orbitals, they are called hybrid orbitals. Each is called an sp orbital, since a merger of an s and a p orbital was required to form it. The sp orbitals, each of which consists of a large lobe and a very small one, are atomic orbitals, although they arise only in the bonding process and... [Pg.6]

There are two simple atomic orbitals i and p orbitals (we don t really deal with d and/orbitals in organic chemistry), i orbitals are spherical and p orbitals have two lobes (one front lobe and one back lobe) ... [Pg.75]

Figure 10.4 Shapes of the s, p, and d atomic orbitals. The s orbital (a) is spherically symmetrical about the nucleus. The three p orbitals (b) are figure-of-eight lobes orientated along the three orthogonal axes (only z axis shown). The five d orbitals (c, d, and e) are four quatrefoil lobes, one orientated along the x-y axes, three between the axes, and the fifth (e) a figure-of-eight along the z axis with an additional donut around the nucleus. The orbitals are not drawn to the same scale. Figure 10.4 Shapes of the s, p, and d atomic orbitals. The s orbital (a) is spherically symmetrical about the nucleus. The three p orbitals (b) are figure-of-eight lobes orientated along the three orthogonal axes (only z axis shown). The five d orbitals (c, d, and e) are four quatrefoil lobes, one orientated along the x-y axes, three between the axes, and the fifth (e) a figure-of-eight along the z axis with an additional donut around the nucleus. The orbitals are not drawn to the same scale.
It is to be noted that o orbitals are formed not only by the overlap of two 5 orbitals but by the overlap of any of the atomic orbitals (s, p. d or f) whether same or different, but the two lobes must have the same sign. A + s orbital can form a bond only by overlapping with another positive 5 orbital or with a + lobe of a p, d or / orbital. [Pg.25]

The orbital angular-momentum quantum number, , defines the shape of the atomic orbital (for example, s-orbitals have a spherical boundary surface, while p-orbitals are represented by a two-lobed shaped boundary surface). can have integral values from 0 to (n - 1) for each value of n. The value of for a particular orbital is designated by the letters s, p, d and f, corresponding to values of 0, 1, 2 and 3 respectively (Table 1.2). [Pg.7]

The principal quantum number n is the most important determinant of the radius and energy of the electron atomic orbital. The orbital shape quantum number I determines the shape of the atomic orbital. When / = 1, the atomic orbital is called an s orbital there are two s orbitals for each value of n, and they are spherically symmetric in space around the nucleus. When I = 2, the orbitals are called the p orbitals there are six p orbitals, and they have a dumbbell shape of two lobes that are diametrically opposed. When I = 3 and 4, we have 10 d orbitals and 14 f orbitals. The orbital orientation quantum number m controls the orientation of the orbitals. For the simplest system of a single electron in a hydrogen atom, the most stable wave function Is has the following form ... [Pg.74]

The trick is to make two equivalent orbitals in Be out of the atomic orbitals so that each hydrogen will see essentially the same electronic environment. We can accomplish this by mixing the 2s orbital and one of the empty 2p orbitals (say, the 2p ) to form two equivalent orbitals we call sp" hybrids, since they have both s and p characteristics. As with molecular orbital theory, we have to end up with the same number of orbitals we started with. The bonding lobes on the new spa and spb orbitals on Be are 180° apart, just as we need to form BeH2. In this manner, we can mix any type of orbitals we wish to come up with specific bond angles and numbers of equivalent orbitals. The most common combinations are sp, sp, and sp hybrids. In sp hybrids, one and one p orbital are mixed to get two sp orbitals, both of which... [Pg.24]

Problem 8.55 (a) Apply the MO theory to the C==C—C=C—C carbocation, considering the signs of the upper lobes of adjacent p atomic orbitals (f>) Indicate the relative energies of the molecular orbitals and state if they are bonding, nonbonding, or antibonding, (c) Show the distribution of the n electrons. ... [Pg.165]

The Schrodinger equation is a differential equation, which means that solutions of it are themselves equations. The solutions, however, are not differential equations, but simple equations for which graphs can be drawn. Such graphs, which are three-dimensional pictures that show the electron density, are called orbitals or electron clouds. Most students are familiar with the shapes of the s and p atomic orbitals (Figure 1.1). Note that each p orbital has a node—a region in space where the probability of finding the electron is extremely small.2 Also note that in Figure 1.1 some lobes of the orbitals are labeled + and others -. ... [Pg.2]

An atomic orbital represents an energy level for an electron. Because there are many different energy levels for an electron, we find there are many different atomic orbitals. As Table 5-1 shows, atomic orbitals come in a variety of shapes, some quite exquisite. We categorize these orbitals by their complexity using the letters s, p, d, and f. The simplest is the spherical s orbital. The p orbital consists of two lobes and resembles an hourglass. There are three kinds ofp orbitals, and they differ from one another only by their orientation in three-dimensional space. The more complex d orbitals have five possible shapes, and the/orbitals have seven. Please do not memorize all the orbital... [Pg.158]

Another factor which affects the most stable arrangement of the atom in a molecule is the variation of bond energy with hybridization. The directed lobes of s-p hybrid orbitals overlap more effectively than the undirected s orbitals, the two-lobed p orbitals, or the diffuse if orbitals. The increased overlap results in stronger bonds... [Pg.125]


See other pages where Lobes, atomic orbital is mentioned: [Pg.22]    [Pg.807]    [Pg.941]    [Pg.3]    [Pg.4]    [Pg.7]    [Pg.1430]    [Pg.222]    [Pg.663]    [Pg.9]    [Pg.343]    [Pg.212]    [Pg.9]    [Pg.343]    [Pg.22]    [Pg.3]    [Pg.125]    [Pg.751]    [Pg.761]    [Pg.219]    [Pg.386]    [Pg.291]    [Pg.5]    [Pg.76]    [Pg.265]    [Pg.4]    [Pg.5]    [Pg.7]    [Pg.1114]    [Pg.222]    [Pg.389]    [Pg.636]    [Pg.265]    [Pg.288]    [Pg.1024]    [Pg.1024]    [Pg.579]   
See also in sourсe #XX -- [ Pg.13 , Pg.14 ]

See also in sourсe #XX -- [ Pg.14 ]

See also in sourсe #XX -- [ Pg.13 ]




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