Why are CFC-Gases Inert Despite Their High Electronegativity?

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The discussion centers on the stability of certain halogenated compounds, particularly 1,2-dichloro-3,4-difluoromethane, and the reasons behind their lack of reactivity. The stability is attributed to the strong carbon-fluorine bonds and the polar nature of the molecule, which results from the electronegativity of the halogens. The presence of multiple electronegative atoms creates a significant positive charge on the carbon, raising questions about the potential for substitution reactions and the role of halogens as leaving groups. The conversation seeks clarification on bond enthalpies, specifically for compounds like CFC-11, to better understand the underlying chemistry of these stable gases.
Chem.Stud.
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I've been thinking about this for some time now, and I can't find anything specific on it on the interwebs.

Clearly, these gases are very stable, or else they would react. But why stable? Can it really be so beneficial for, let's say, 1,2-dichloro-3,4-difluoromethane to have so kany electronegative atoms bonded to the carbon? The molecule would be very polar with a relatively big plsitive charge on the carbon atom. I would think that one of the halogens would make a good leaving group in substitution...

I'm lost, could someone please help me out? :)
 
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I think it has to be with very strong bonds between C and the halogens. The halogens are pulling very much on the electrons, which makes the molecule very polar, and the bonds very strong.

But if someone else could confirm, and go a little more in-depth, you'd probably be better off. What's the bond enthalpies for a "normal" CFC? For CFC-11, for example?
 
Chem.Stud. said:
I've been thinking about this for some time now, and I can't find anything specific on it on the interwebs.

Clearly, these gases are very stable, or else they would react. But why stable? Can it really be so beneficial for, let's say, 1,2-dichloro-3,4-difluoromethane to have so kany electronegative atoms bonded to the carbon? The molecule would be very polar with a relatively big plsitive charge on the carbon atom. I would think that one of the halogens would make a good leaving group in substitution...

I'm lost, could someone please help me out? :)

They are characterized by strong carbon–fluorine bonds
 
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