Understanding the Hybridization and Formation of Pi Bonds in Ammonia and Ethyne

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SUMMARY

The discussion clarifies the hybridization of nitrogen in ammonia (NH3) as sp3 due to the presence of four electron pairs, including a lone pair. In ethyne (H-C≡C-H), the formation of two pi bonds occurs through the overlap of the unhybridized 2px and 2py orbitals of carbon atoms, while the 2pz orbital remains unutilized for pi bonding. The confusion regarding energy levels of orbitals is addressed, emphasizing that hybridization alters the energy levels of the orbitals involved in bonding.

PREREQUISITES
  • Understanding of hybridization concepts in chemistry
  • Familiarity with molecular orbital theory
  • Knowledge of electron configurations, particularly for carbon and nitrogen
  • Basic grasp of sigma and pi bonds
NEXT STEPS
  • Study the concept of hybridization in greater detail, focusing on sp, sp2, and sp3 hybridizations
  • Learn about molecular orbital theory and its implications for bonding
  • Investigate the differences in energy levels of orbitals in isolated versus bonded atoms
  • Explore examples of hybridization in other molecules beyond ammonia and ethyne
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Chemistry students, educators, and professionals seeking to deepen their understanding of molecular bonding and hybridization concepts.

Clari
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In ammonia, why the N atom is sp3 hybridized and not sp2 hybridized...since there are only 3 bondings...

Also, in ethyne, that is H-C(triple bond)C-H...for the formation of 2 pi bonds, why it is the unhybridized 2px orbital and 2py orbital of each C atom overlap with each other? How about the 2pz orbital?


any help would be appreciated
 
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In NH3, there are 4 electron pairs about the N atom - you're omitting the lone pair.

The triple bond in H-C \equiv C-H is basically a sigma bond using one of the two 2s electrons (the other 2s electron is used for the sigma bond with H), and a pair of pi bonds using both of the 2p electrons. Since C has only 2 electrons in the 2p subshell, and since px and py are lower energy orbitals than pz, the pi bonds must involve an overlap of only these orbitals.
 
Gokul43201:

but in my textbook, it is said that orbitals in the same subshell is at the same energy level...I am confused now...
 
Clari said:
Gokul43201:

but in my textbook, it is said that orbitals in the same subshell is at the same energy level...I am confused now...

For isolated Carbon atoms they do:2p_{x},2p_{y} & 2p_{z} have all the same energy.But when the Carbon atom reacts with nonmetalic elements,like Hydrogen,those orbitals do not behave in the same manner.That's because 2 of them have one electron and the remaining one (2p_{z}) has none.The 2 orbitals with one electron they "hybridize" with the 2s orbital which has 2 electrons,resulting in 4 hybridized orbitals of smaller energy than the unhybridized 2p_{z}.Since it overlaps 3 hybrid orbitals (one \sigma and 2 \pi) with another C atom,it has a triple bond.Since 2 of the bonds are \pi,and another 2 are \sigma,it id hybridized sp.


Daniel.

PS.Maybe Gokul can put it in a more coherent way... :wink:
 
As Dexter mentioned, your textbook is right only when it talks about isolated atoms.

However, when a molecule is being formed, the direction along the line joining the atoms breaks the degeneracy (x, y and z are not symmetric anymore; the z direction is the internuclear direction and so, is different from x and y) between px, py and pz.
 
A "pz" pi molecular orbital would be along the same axis as the sigma, perhaps this clarifies things a bit more.
 

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