Why won't water molecules dissociate?

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Discussion Overview

The discussion revolves around the dissociation of water molecules, specifically addressing why pure water is not considered an electrolyte and the nature of the ions produced when water does dissociate. Participants explore theoretical and conceptual aspects of water ionization, solvation, and the behavior of protons in aqueous solutions.

Discussion Character

  • Exploratory
  • Technical explanation
  • Conceptual clarification
  • Debate/contested

Main Points Raised

  • Some participants assert that pure water does not dissociate into charged particles, while others clarify that it does dissociate into H+ and OH- ions, albeit at low concentrations.
  • A participant emphasizes that the dissociation should be represented by the equilibrium equation 2H2O (l) ⇔ H3O+ (aq) + OH- (aq), noting that H+ is often used for simplification.
  • Another participant discusses the solvation of protons by multiple water molecules, suggesting that H+ and H3O+ are not fully representative of the reality in solution.
  • There is a question about the size of the solvated clusters, with some suggesting that the number of water molecules (n) surrounding a proton can be significant, potentially up to 20, while others express uncertainty about what constitutes a "large" n.
  • Participants discuss the differences in bonding between protons in H3O+ and those in larger clusters, noting that the latter are bound via hydrogen bonds rather than covalent bonds.
  • One participant mentions the symmetry of small water clusters and how it may change as the size of the cluster increases.

Areas of Agreement / Disagreement

Participants do not reach a consensus on the nature of water dissociation and the representation of ions in solution. Multiple competing views remain regarding the interpretation of dissociation, solvation, and the characteristics of proton clusters.

Contextual Notes

The discussion includes assumptions about the definitions of dissociation and solvation, as well as varying interpretations of what constitutes a significant number of solvating water molecules. There are unresolved questions about the behavior of protons in solution and the implications of different bonding types.

Lim Y K
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Pure water is not an electrolyte. This is because the hydrogen atoms and oxygen atom will not dissociate into individual charged particles. Why won't they dissociate?
 
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They do dissociate, as described by a water ion product. However, concentrations of H+ and OH- thus produced are quite low, so the specific resistance of a pure water is quite high (18 MΩ).
 
Besides, that's not two atoms'( ##\text{H}## and ##\text{O}## ) dissociation, but ##\text{H}^+## and ##\text{OH}^-.##
 
tommyxu3 said:
Besides, that's not two atoms'( ##\text{H}## and ##\text{O}## ) dissociation, but ##\text{H}^+## and ##\text{OH}^-.##
Isn't the actual ionic equilibrium ##2H_2 O (l) ⇔ H_3 O^{+} (aq)+ OH^{-} (aq) ## ? If I remember correctly, H+ ions are just used instead of hydronium ion for simplification of the equation, but the actual equation is the one above.
 
Protons can be solvated by several water molecules (so there exists whole series of cations of the general formula H2n+1On+). H+ is about as good as H3O+ IMHO - works OK as a symbol, doesn't reflect the reality. Add to that fact that OH- is not isolated in the solution, but solvated as well (yielding H2n+1On+1- anions), and you should start to see the picture :wink:
 
Borek said:
Protons can be solvated by several water molecules (so there exists whole series of cations of the general formula H2n+1On+). H+ is about as good as H3O+ IMHO - works OK as a symbol, doesn't reflect the reality. Add to that fact that OH- is not isolated in the solution, but solvated as well (yielding H2n+1On+1- anions), and you should start to see the picture :wink:
Ahh, I see. But is it safe to say that n is not large? I mean after all, you'll eventually crowd up the entire area around the H+ ion so that the repulsion between the lone pair of electrons on the O atoms of water molecules solvating the ion and the lone pairs on the O atoms of 'unlinked' water molecules is greater than any attractive force the 'unlinked' water molecules might feel toward the H+ ion, preventing these 'unlinked' molecules from solvating the H+ ion as well.
P.S. I can't find a replacement word for 'unlinked' from my Chemistry verbiage memory bank right now :P
 
Borek said:
Protons can be solvated by several water molecules (so there exists whole series of cations of the general formula H2n+1On+). H+ is about as good as H3O+ IMHO - works OK as a symbol, doesn't reflect the reality. Add to that fact that OH- is not isolated in the solution, but solvated as well (yielding H2n+1On+1- anions), and you should start to see the picture :wink:

I think the difference is that in H3O+, the proton is covalently bounded to a water molecule while the additional water molecules in the larger clusters are bound via hydrogen bridges.
 
  • #10
DrDu said:
I think the difference is that in H3O+, the proton is covalently bounded to a water molecule while the additional water molecules in the larger clusters are bound via hydrogen bridges.

I would expect the change to be gradual - for small n (like 2 or 3) I would guess the cluster to be quite symmetrical, and all water molecules to be equivalent. Once the structure gets larger the outer layers will be definitely bonded differently.
 
  • #11
The only symmetric hydrogen bond I know about is the FHF-. So even in small water clusters, you can uniquely define which one is the hydronium ion.
 

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