Hybridisation of Chromate Ion Explained

In summary: So how do we identify the complex?Chromate ion is a complex, and the simplest way to identify it is to look at the molecular formula.
  • #1
Karan Punjabi
127
3
Can some one explain the structure of chromate ion on the basis of hybridisation cause I'm a bit confused I googled about it and there are posts like explaining it as sp3 hybridised ion. Explain please.
 
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  • #2
Karan Punjabi said:
Can some one explain the structure of chromate ion on the basis of hybridisation cause I'm a bit confused I googled about it and there are posts like explaining it as sp3 hybridised ion. Explain please.
Guys please help me.
 
  • #3
If you really want to describe transition metal compounds in terms of hybrids, I would rather go for ##d^3s## than ##sp^3##, as the p orbitals in a highly charged ion like chromium VI are energetically much higher than the d orbitals. The d3s hybrids are directed along the diagonals of a cube. If you allow for a small substitution of d for p, the two directions along the diagonal become unequal and you will get a more tetrahedral shape.
 
  • #4
DrDu said:
If you really want to describe transition metal compounds in terms of hybrids, I would rather go for ##d^3s## than ##sp^3##, as the p orbitals in a highly charged ion like chromium VI are energetically much higher than the d orbitals. The d3s hybrids are directed along the diagonals of a cube. If you allow for a small substitution of d for p, the two directions along the diagonal become unequal and you will get a more tetrahedral shape.
The inner s orbital ie 3s would be affected by hybridisation or not? And how we are considering hybridisation between 2 orbitals of different shells?
 
  • #5
The inner 3s orbital is way too low in energy and completely filled. Hence it won't participate in bonding. There is no prinicpal difficulty with hybridizing orbitals of different sub-shells as long as they are of comparable energy and size.
 
  • #6
DrDu said:
The inner 3s orbital is way too low in energy and completely filled. Hence it won't participate in bonding. There is no prinicpal difficulty with hybridizing orbitals of different sub-shells as long as they are of comparable energy and size.
Got it. One more thing chromate ion is a complex right?
 

FAQ: Hybridisation of Chromate Ion Explained

What is hybridisation of chromate ion?

The hybridisation of chromate ion is a chemical process in which the electrons of the chromate ion are rearranged to form new molecular orbitals with different energies and shapes. This process allows the chromate ion to bond with other atoms and molecules, creating new compounds.

What is the structure of chromate ion?

The chromate ion has a tetrahedral structure, with four oxygen atoms bonded to a central chromium atom. The four oxygen atoms are arranged at the corners of a tetrahedron, with the chromium atom at the center.

Why does chromate ion undergo hybridisation?

Chromate ion undergoes hybridisation in order to achieve a more stable electronic configuration. By rearranging its electrons, the chromate ion can achieve a lower energy state, making it more stable and less reactive.

What are the types of hybridisation in chromate ion?

There are two types of hybridisation that can occur in chromate ion: sp3 and sp2. In sp3 hybridisation, the four oxygen atoms are arranged at equal distances from the central chromium atom, forming a tetrahedral shape. In sp2 hybridisation, three of the oxygen atoms are arranged in a plane, with the fourth oxygen atom perpendicular to the plane.

How does hybridisation affect the properties of chromate ion?

The type of hybridisation in chromate ion can affect its properties, such as its chemical reactivity and bond angles. For example, sp3 hybridisation results in a more stable and less reactive chromate ion, while sp2 hybridisation results in a more reactive and less stable ion. Additionally, the bond angles in sp3 hybridised chromate ion are closer to 109.5 degrees, while those in sp2 hybridised chromate ion are closer to 120 degrees.

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