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By the end of this section, you will be able to:
  • Describe multiple covalent bonding in terms of atomic orbital overlap
  • Relate the concept of resonance to π-bonding and electron delocalization

The hybrid orbital model appears to account well for the geometry of molecules involving single covalent bonds. Is it also capable of describing molecules containing double and triple bonds? We have already discussed that multiple bonds consist of σ and π bonds. Next we can consider how we visualize these components and how they relate to hybrid orbitals. The Lewis structure of ethene, C 2 H 4 , shows us that each carbon atom is surrounded by one other carbon atom and two hydrogen atoms.

A Lewis structure is shown in which two carbon atoms are bonded together by a double bond. Each carbon atom is bonded to two hydrogen atoms by a single bond.

The three bonding regions form a trigonal planar electron-pair geometry. Thus we expect the σ bonds from each carbon atom are formed using a set of sp 2 hybrid orbitals that result from hybridization of two of the 2 p orbitals and the 2 s orbital ( [link] ). These orbitals form the C–H single bonds and the σ bond in the C = C double bond ( [link] ) . The π bond in the C = C double bond results from the overlap of the third (remaining) 2 p orbital on each carbon atom that is not involved in hybridization. This unhybridized p orbital (lobes shown in red and blue in [link] ) is perpendicular to the plane of the sp 2 hybrid orbitals. Thus the unhybridized 2 p orbitals overlap in a side-by-side fashion, above and below the internuclear axis ( [link] ) and form a π bond .

A diagram is shown in two parts, connected by a right facing arrow labeled, “Hybridization.” The left diagram shows an up-facing arrow labeled, “E.” To the lower right of the arrow is a short, horizontal line labeled, “2 s,” that has two vertical half-arrows facing up and down on it. To the upper right of the arrow are a series of three short, horizontal lines labeled, “2 p.” Above both sets of lines is the phrase, “Orbitals in an isolated C atom.” Two of the lines have vertical, up-facing arrows drawn on them. The right side of the diagram shows three short, horizontal lines placed halfway up the space and each labeled, “s p superscript 2.” An upward-facing half arrow is drawn vertically on each line. Above these lines is one other short, horizontal line, labeled, “p.” Above both sets of lines is the phrase, “Orbitals in the s p superscript 2 hybridized C atom in C subscript 2 H subscript 4.”
In ethene, each carbon atom is sp 2 hybridized, and the sp 2 orbitals and the p orbital are singly occupied. The hybrid orbitals overlap to form σ bonds, while the p orbitals on each carbon atom overlap to form a π bond.
Two diagrams are shown labeled, “a” and “b.” Diagram a shows two carbon atoms with three purple balloon-like orbitals arranged in a plane around them and two red balloon-like orbitals arranged vertically and perpendicularly to the plane. There is an overlap of two of the purple orbitals in between the two carbon atoms, and the other four purple orbitals that face the outside of the molecule are shown interacting with spherical blue orbitals from four hydrogen atoms. Diagram b depicts a similar image to diagram a, but the red, vertical orbitals are interacting above and below the plane of the molecule to form two areas labeled, “One pi bond.”
In the ethene molecule, C 2 H 4, there are (a) five σ bonds. One C–C σ bond results from overlap of sp 2 hybrid orbitals on the carbon atom with one sp 2 hybrid orbital on the other carbon atom. Four C–H bonds result from the overlap between the C atoms' sp 2 orbitals with s orbitals on the hydrogen atoms. (b) The π bond is formed by the side-by-side overlap of the two unhybridized p orbitals in the two carbon atoms. The two lobes of the π bond are above and below the plane of the σ system.

In an ethene molecule, the four hydrogen atoms and the two carbon atoms are all in the same plane. If the two planes of sp 2 hybrid orbitals tilted relative to each other, the p orbitals would not be oriented to overlap efficiently to create the π bond. The planar configuration for the ethene molecule occurs because it is the most stable bonding arrangement. This is a significant difference between σ and π bonds; rotation around single (σ) bonds occurs easily because the end-to-end orbital overlap does not depend on the relative orientation of the orbitals on each atom in the bond. In other words, rotation around the internuclear axis does not change the extent to which the σ bonding orbitals overlap because the bonding electron density is symmetric about the axis. Rotation about the internuclear axis is much more difficult for multiple bonds; however, this would drastically alter the off-axis overlap of the π bonding orbitals, essentially breaking the π bond.

Questions & Answers

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Source:  OpenStax, Chemistry. OpenStax CNX. May 20, 2015 Download for free at http://legacy.cnx.org/content/col11760/1.9
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