1.9 sp Hybrid Orbitals and the Structure of Acetylene
In addition to forming single and double bonds by sharing two and four electrons, respectively, carbon can also form a triple bond by sharing six electrons. To account for the triple bond in a molecule such as acetylene, H−C≡C−H, we need a third kind of hybrid orbital, an sp hybrid. Imagine that, instead of combining with two or three p orbitals, a carbon 2s orbital hybridizes with only a single p orbital. Two sp hybrid orbitals result, and two p orbitals remain unchanged. The two sp orbitals are oriented 180° apart on the right- left (x) axis, while the p orbitals are perpendicular on the up-down (y) axis and the in-out
(z) axis, as shown in Figure 1.16.

Figure 1.16 sp Hybridization. The two sp hybrid orbitals are oriented 180° away from each other, perpendicular to the two remaining p orbitals (red/blue).
When two sp-hybridized carbon atoms approach each other, sp hybrid orbitals on each carbon overlap head-on to form a strong sp–sp σ bond. At the same time, the pz orbitals from each carbon form a pz–pz π bond by sideways overlap, and the py orbitals overlap similarly to form a py–py π bond. The net effect is the sharing of six electrons and formation of a carbon–carbon triple bond. Each of the two remaining sp hybrid orbitals forms a σ bond with hydrogen to complete the acetylene molecule (Figure 1.17).

Figure 1.17 The structure of acetylene. The two carbon atoms are joined by one sp–sp σ
bond and two p–p π bonds.
As suggested by sp hybridization, acetylene is a linear molecule with H–C–C bond angles of 180°. The C–H bonds have a length of 106 pm and a strength of 558 kJ/mol (133 kcal/mol). The C–C bond length in acetylene is 120 pm, and its strength is about 965 kJ/mol (231 kcal/mol), making it the shortest and strongest of any carbon–carbon bond. A comparison of sp, sp2, and sp3 hybridization is given in Table 1.2.
Table 1.2Comparison of C−C and C−H Bonds in Methane, Ethane, Ethylene, and Acetylene
| Bond | Bond strength | Bond length (pm) | ||
| (kJ/mol) | (kcal/mol) | |||
| Methane, CH4 | (sp3) C−H | 439 | 105 | 109 | 
| Ethane, CH3CH3 | (sp3) C−C (sp3) | 377 | 90 | 153 | 
| (sp3) C−H | 421 | 101 | 109 | |
| Ethylene, H2C=CH2 | (sp2) C=C (sp2) | 728 | 174 | 134 | 
| (sp2) C−H | 464 | 111 | 109 | |
| Acetylene, HC≡CH | (sp) C≡C (sp) | 965 | 231 | 120 | 
| (sp) C−H | 558 | 133 | 106 | |
Problem 1-13
Draw a line-bond structure for propyne, CH3C≡CH. Indicate the hybridization of the orbitals on each carbon, and predict a value for each bond angle.
