Assumptions Built in to Solving Titration Equilibria?

AI Thread Summary
The discussion focuses on understanding the assumptions made when calculating equilibrium concentrations in acid-base reactions, specifically using the example of mixing equal concentrations of NH3 and HCl. It highlights the assumption that HCl, a strong acid, fully ionizes, leading to the formation of NH4+ from NH3 and H3O+. The participant questions whether this assumption is valid, considering that some hydrogen ions might remain as H3O+, potentially affecting the concentration of NH4+. Additionally, the discussion raises concerns about the oversimplification of scenarios in equilibrium problems, suggesting that while the results are often close to reality, the underlying assumptions may not always hold true. A recommendation is made to explore resources that detail the general case of acid/base equilibrium without simplifications, emphasizing the importance of understanding when and why these assumptions are applicable.
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I'm trying to reach a more thorough understanding of what's going on when we calculate equilibrium concentrations and was wanting to understand more what assumptions we make in order to follow through with the calculations.

Let me ask off of an example:
Consider mixing equal amounts of NH3 and HCl, each having the concentration of α upon mixing.

The general way I've seen taught is to assume via being a strong acid that the HCl fully ionizes and causes the following equation to occur:
NH3 + H30+ → NH4+ + H2O
Then to recognize that NH4+ is a weak acid, so we'll need to set up the reverse equation as an equilibrium to run an ICE problem off of:
NH4+ + H2O ←→ NH3 + H30+
Wherein we take the initial concentration of NH4+ to be α, and can use it's Ka to find the final hydrogen ion concentration of the entire solution.

Here then are my questions directly:
1) In the first equation, we seem to assume that all the hydrogen ions from HCl jump onto our NH3, thus allowing us to use our initial α concentration also as the initial concentration of NH4+. How so? Could it not be that some hydrogen ions tend to stick around as H30+, thereby reducing the actual concentration of NH4+ to slightly less than α? What knowledge/assumptions do we use to reduce this complexity from our calculations?
2) Are there any other important assumptions we make when working similar equilibrium problems? As I work them myself, I constantly feel like the scenarios are a bit oversimplified (even if I acknowledge they give us answers very proximal to reality).

Thanks much!
 
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I strongly suggest you go through the http://www.chembuddy.com/?left=pH-calculation&right=toc

Not only it shows how to solve the general case of acid/base equilibrium without any simplifying assumptions, but it also shows what the simplifications are in practical working of many cases. Once you know what the general approach is you should be able to understand why and when simplifying assumptions work (and when and why they don't).
 
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