Use molecular orbital theory to complete the ground state electron configuration for each of the molecules. Molecule NF NF+ NF NF bond order: Ground state electron configuration NF+ bond order: Determine the bond order of each of the molecules. Answer Bank 3 Question source: McQuarrie, Rock, And Gallogly 4e – General Chemistry

The Correct Answer and Explanation is:

To solve this problem using molecular orbital (MO) theory, we will examine the molecular orbital configurations of NF and NF⁺ and determine their bond orders.


Step 1: Determine the total number of electrons

  • N (Nitrogen) has 7 electrons
  • F (Fluorine) has 9 electrons
  • So, NF has 7 + 9 = 16 electrons
  • NF⁺ loses one electron → 15 electrons

Step 2: Use the MO energy diagram for heteronuclear diatomic molecules

NF is a heteronuclear diatomic molecule. The molecular orbital ordering resembles that of oxygen and fluorine molecules (because F dominates in electronegativity). The orbital energy order is:

scssCopyEditσ(1s), σ*(1s), σ(2s), σ*(2s), σ(2p), π(2p), π*(2p), σ*(2p)

Step 3: Fill the molecular orbitals

For NF (16 electrons):

Fill the orbitals in order:

  • σ(1s)²
  • σ*(1s)²
  • σ(2s)²
  • σ*(2s)²
  • σ(2p)²
  • π(2p)⁴
  • π*(2p)²

Bond Order = ½ × [(# of bonding electrons) − (# of antibonding electrons)]
= ½ × [(2 + 2 + 2 + 4) − (2 + 2 + 2)]
= ½ × [10 − 6]
= 2


For NF⁺ (15 electrons):

Remove one electron from the highest energy orbital (π*(2p)):

  • σ(1s)²
  • σ*(1s)²
  • σ(2s)²
  • σ*(2s)²
  • σ(2p)²
  • π(2p)⁴
  • π*(2p)¹

Bond Order = ½ × [(10) − (5)] = 2.5


Final Answers:

  • NF bond order: 2
  • NF⁺ bond order: 2.5

Ground State Electron Configurations:

NF (16e⁻):
σ(1s)² σ*(1s)² σ(2s)² σ*(2s)² σ(2p)² π(2p)⁴ π*(2p)²

NF⁺ (15e⁻):
σ(1s)² σ*(1s)² σ(2s)² σ*(2s)² σ(2p)² π(2p)⁴ π*(2p)¹


Explanation:

Molecular orbital theory combines atomic orbitals to form molecular orbitals that are spread over the entire molecule. Electrons fill lower-energy bonding orbitals before entering higher-energy antibonding orbitals. A bond order reflects the net bonding strength between atoms: the higher the bond order, the stronger the bond. In this case, NF⁺ has a higher bond order than NF, which means removing an electron (from an antibonding orbital) actually strengthens the bond. This is a good illustration of how molecular orbital theory can predict trends in bond strength based on electron configuration.

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