In which of the following molecules would you expect to find delocalized molecular orbitals: (a) \(\mathrm{C}_{2} \mathrm{H}_{4}\) (b) \(\mathrm{SO}_{2} ;\) (c) \(\mathrm{H}_{2} \mathrm{CO}\) ? Explain.

Short Answer

Expert verified
Delocalized molecular orbitals are present in Ethene (\(\mathrm{C}_{2} \mathrm{H}_{4}\)) and Sulfur Dioxide (\(\mathrm{SO}_{2}\)) but not in Formaldehyde (\(\mathrm{H}_{2} \mathrm{CO}\)).

Step by step solution

01

Understanding Delocalized Orbitals

Delocalized molecular orbitals extend over three or more atoms. They contribute to the stability of molecules and are usually present in molecules that exhibit resonance.
02

Analyzing Ethene \(\mathrm{C}_{2} \mathrm{H}_{4}\)

In ethene, which is a planar and symmetrical molecule, the six electrons from the carbon atoms are localized in three sigma bonds, two with hydrogen and one with the carbon atom. The remaining electron in each carbon forms a pi bond, which is a delocalized molecular orbital
03

Analyzing Sulfur Dioxide \(\mathrm{SO}_{2}\)

In sulfur dioxide, sulfur forms one sigma bond with each oxygen atom, and one of the oxygen atoms forms a pi bond with sulfur. However, the molecule has resonance structures, which means that the pi bond electrons are spread over three atoms making them delocalized.
04

Analyzing Formaldehyde \(\mathrm{H}_{2} \mathrm{CO}\)

In formaldehyde, carbon forms sigma bonds with hydrogen and oxygen, and forms a pi bond with oxygen. The pi bond is localized between carbon and oxygen, and there are no resonating structures. Therefore, there are no delocalized electrons in formaldehyde.

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