Sigma Percentile
JEE Main 2019
LEVELJEE Advanced

Animated Solution for Chemistry - Chemical Bonding and Molecular Structure: In which of the following processes, the bond order has increased and paramagnetic character has changed to diamagnetic?

Select Answer:

Visualized Solution

Problem Analysis

  • Find the process where:
  • 1. Bond Order () increases.
  • 2. Magnetic nature changes from Paramagnetic to Diamagnetic.

Key Concepts of MOT

  • Bond Order () =
  • Paramagnetic: Has unpaired electrons.
  • Diamagnetic: All electrons are paired.

Option (a):

  • (): , Paramagnetic (2 unpaired )
  • (): , Paramagnetic (1 unpaired )
  • BO increases, but remains Paramagnetic. (Incorrect)

Option (b):

  • (): , Diamagnetic (0 unpaired )
  • (): , Paramagnetic (1 unpaired )
  • BO decreases, becomes Paramagnetic. (Incorrect)

Option (c):

  • (): , Paramagnetic
  • (): , Diamagnetic
  • Becomes Diamagnetic, but BO decreases. (Incorrect)

Option (d):

  • (): , Paramagnetic
  • (): , Diamagnetic
  • BO increases AND becomes Diamagnetic. (Correct!)

Visualizing the Transition

  • Removing an electron from the antibonding orbital:
  • 1. Decreases Increases .
  • 2. Removes the only unpaired electron Becomes Diamagnetic.

Final Conclusion

  • The correct process is

The Sigma Insight: Molecular Orbital Theory

Solution Diagram

The Quest for Stability

Imagine you are an architect of molecules. Your goal is to find a specific transformation where a molecule not only becomes more tightly bound together but also pairs up all its lonely, unpaired electrons.
In the language of chemistry, we are looking for a process where the Bond Order (BO) increases, and the magnetic nature shifts from paramagnetic to diamagnetic.
To solve this, we need our trusty blueprint: Molecular Orbital Theory (MOT).

The Master Equations

Before we dive into the options, let's recall the fundamental rules of MOT.
The strength of a bond is measured by its Bond Order, calculated as:
where is the number of bonding electrons and is the number of antibonding electrons.
Key Principle: Adding electrons to bonding orbitals or removing them from antibonding orbitals will increase the bond order.
For the magnetic nature, the rule is simple: If there is even one unpaired electron, the species is paramagnetic. If all electrons are perfectly paired, it is diamagnetic.

Decoding the Options

Let's put each option to the test.
Option (a): The oxygen molecule, , has electrons. Its MO configuration ends with two unpaired electrons in the orbitals, making it paramagnetic with a bond order of .
When it loses an electron to form , the bond order increases to . However, it still has one unpaired electron left. It remains paramagnetic. Close, but not what we need!
Option (b): Nitrogen, , is a highly stable molecule with electrons. All are paired, making it diamagnetic with a maximum bond order of .
Removing an electron to form drops the bond order to and introduces an unpaired electron. It becomes paramagnetic. This is the exact opposite of what we want!
Option (c): Starting again with paramagnetic (), we add two electrons to form the peroxide ion, .
These electrons fill the orbitals, pairing everything up. It successfully becomes diamagnetic! But wait, because we added electrons to antibonding orbitals, the bond order drops to . This option fails the first condition.

The Winning Transition

Option (d): Nitric oxide, , has electrons. Because is an odd number, it is guaranteed to be paramagnetic. Specifically, it has one unpaired electron sitting in the antibonding orbital. Its bond order is .
Now, let's remove an electron to form the nitrosonium ion, .
Where does this electron come from? It is removed from the highest energy orbital, which is that exact antibonding orbital!
By removing an antibonding electron, decreases.
The bond order increases from to !
Furthermore, the only unpaired electron is now gone. has electrons, making it isoelectronic with . All electrons are paired, so it is perfectly diamagnetic.
Both conditions are flawlessly met. The correct process is indeed .

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