Sp3 hybridized

An answer was provided in 1931 by Linus Pauling, who showed how an s orbital and three p orbitals on an atom can combine mathematically, or hybridize, to form four equivalent atomic orbitals with tetrahedral orientation. Shown in Figure 1.10, these tetrahedrally oriented orbitals are called sp3 hybrids. Note that the superscript 3 in the name sp3 tells how many of each type of atomic orbital combine to form the hybrid, not how many electrons occupy it. 

The concept of hybridization explains how carbon forms four equivalent tetrahedral bonds but not why it does so. The shape of the hybrid orbital suggests the answer. When an 5 orbital hybridizes rvith three p orbitals, the resultant sp3 hybrid orbitals are unsyimmetrical about the nucleus. One of the two... 

Although sp3 hybridization is the most common electronic state of carbon, it s not the only possibility. Look at ethylene, C2H4, for example. It was recognized more than 100 years ago that ethylene carbons can be tetravalent only if they share four electrons and are linked by a double bond. Furthermore, ethylene is planar (flat) and has bond angles of approximately 120° rather than 109.5°. 

When we discussed sp3 hybrid orbitals in Section 1.6, we said that the four valence-shell atomic orbitals of carbon combine to form four equivalent sp3 hybrids. Imagine instead that the 2s orbital combines with only two of the three available 2p orbitals. Three sp2 hybrid orbitals result, and one 2p orbital remains unchanged- The three sp2 orbitals lie in a plane at angles of 120° to one another, with the remaining p orbital perpendicular to the sp2 plane, as shown in Figure 1.13. 

Like the carbon atom in methane and the nitrogen atom in methylamine, the oxygen atom in methanol (methyl alcohol) and many other organic molecules can also be described as sp3-hybridized. The C-O-H bond angle in methanol is 108.5°, very close to the 109.5° tetrahedral angle. Two of the four sp3 hybrid... 

Sulfur is most commonly encountered in biological molecules either in compounds called thiols, which have a sulfur atom bonded to one hydrogen and one carbon, or in sulfides, which have a sulfur atom bonded to two carbons. Produced by some bacteria, methanethiol (CH3SH) is the simplest example of a thiol, and dimethyl sulfide [(ChP S l is the simplest example of a sulfide. Both can be described by approximate sp3 hybridization around sulfur, although both have significant deviation from the 109.5° tetrahedral angle. 

In addition to compounds with planar, sp2-hybridized carbons, compounds with tetrahedral, sp3-hybridized atoms can also be prochiral. An vp3-hybridizec) atom is said to be a prochirality center if, by changing one of its attached groups, it becomes a chirality center. The —GH2OH carbon atom of ethanol, for instance, is a prochirality center because changing one of its attached -H atoms converts it into a chirality center. 

A molecule is prochiral if can be converted from achiral to chiral in a single chemical step. A prochiral sp2-hybridized atom has two faces, described as either Re or Si. An sp3-hybridized atom is a prochirality center if, by changing one of its attached atoms, a chirality center results. The atom whose replacement leads to an R chirality center is pro-R, and the atom whose replacement leads to an S chirality center is pro-S. 

Alkyl halides contain a halogen bonded to a saturated, sp3-hybridized carbon atom. The C-X bond is polar, and alkyl halides can therefore behave as electrophiles. 

Another trend is that sp3-hybridized carbons generally absorb from 0 to 90 8, while sp2 carbons absorb from 110 to 220 8. Carbonyl carbons (C=0) are... 

Table 13.3 shows the correlation of H chemical shift with electronic environment in more detail. In general, protons bonded to saturated, sp3-hybridized carbons absorb at higher fields, whereas protons bonded to s/ 2-hybridized carbons absorb at lower fields. Protons on carbons that are bonded to electronegative atoms, such as N, O, or halogen, also absorb at lower fields. 

Alcohols and phenols have nearly the same geometry around the oxygen atom as water. The R-O—H bond angle has an approximately tetrahedral value (109° in methanol, for example), and the oxygen atom is sp3-hybridized. 

Like a carbonyl group, a nitrile group is strongly polarized and has an electrophilic carbon atom. Nitriles therefore react with nucleophiles to yield 5p2-hybridized imine anions in a reaction analogous to the formation of an sp3-hybridized alkoxide ion by nucleophilic addition to a carbonyl group. 

Humulene. structure of, 202 Hund s rule, 6 sp Hybrid orbitals. 17-18 sp2 Hybrid orbitals, 15. sp3 Hybrid orbitals, 12-14 Hydrate, 701... 

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