Jump to content

Recommended Posts

Posted

Helo

 

How are you ?

 

My question is in the picture attached .

 

Please clarify the answer .

 

Please explain why the answer .

 

Thank you for forum .

1.jpg

  • 2 weeks later...
Posted

i don't know correct ans . but acc. to me its n't because of NO but due to formation of pentavalent ( sp3d hybridization ) transition state (as in your case) which acc. to Werner theory is highly unstable so complex again get its tetravalent state .:rolleyes:

Posted

Unfortunately Vedmecum, it is indeed due to the reversible 1e (bent ) NO and 3e (linear) NO interconversion. There are a number of other ligands which show similar effects eg the indenyl ligand which can flip eta-3 to eta-5. The complexes above are coordinatively unsaturated, the 1e (bent) NO configuration makes them electronically unsaturated 16e species, which then exhibit very low activation energy associative ligand substitution mechanisms

Posted

Vedmecum, The point of the question is the 1e/3e interconversion of the NO ligand. This is a rather common undegraduate organometallic chemistry exam question

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
×
×
  • Create New...

Important Information

We have placed cookies on your device to help make this website better. You can adjust your cookie settings, otherwise we'll assume you're okay to continue.