Chapter 9: Problem 37
Specify which hybrid orbitals are used by carbon atoms in the following species: (a) CO (b) \(\mathrm{CO}_{2},(\mathrm{c}) \mathrm{CN}^{-}\)
Short Answer
Step by step solution
Key Concepts
These are the key concepts you need to understand to accurately answer the question.
sp hybrid orbitals
For example, carbon, an element capable of forming covalent bonds, frequently exhibits sp hybridization when it forms multiple bonds like triple bonds. The sp hybrid orbitals participate in forming sigma (\(\sigma\)) bonds, while the unhybridized p orbitals overlap to create pi (\(\pi\)) bonds. This configuration is usually found in molecules like carbon monoxide (CO), carbon dioxide (CO2), and the cyanide ion (CN⁻). Understanding this helps explain their linear shapes and bonding properties.
carbon monoxide
The remaining two p orbitals on carbon contribute to forming two pi bonds with the p orbitals of oxygen, completing the triple bond structure. The sp hybridization results in a linear molecular geometry, reflecting the nature of the bond between carbon and oxygen.
CO is an example of sp hybridization where significant overlap between atomic orbitals creates strong bonds, contributing to its stability despite being a small molecule. This characteristic explains CO's role as an important ligand in coordination chemistry.
carbon dioxide
The linear shape of CO2 is a direct result of the 180-degree arrangement of these sp hybrid orbitals. Carbon's unhybridized p orbitals form pi bonds with the p orbitals of the oxygen atoms, completing the carbon-oxygen double bonds.
Understanding this hybridization explains how CO2 maintains a linear structure, which is vital for its role in various processes such as photosynthesis and respiration. The sp hybrid orbitals help shed light on the molecule's unique properties, including its non-polarity despite having polar bonds.
cyanide ion
Similar to carbon monoxide, the carbon in CN⁻ uses one of its sp hybrid orbitals to form a strong sigma bond with nitrogen. The remaining p orbitals create two pi bonds with the p orbitals on nitrogen, reinforcing the triple bond strength.
As a result, the cyanide ion is highly stable and linear, a testament to effective sp hybridization. This configuration also contributes to its high toxicity, as the ion can penetrate biological membranes easily. Understanding CN⁻'s structure is critical to grasping its behavior in biological contexts and chemical reactions.