Finding The Concentration Of An Ion

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Discussion Overview

The discussion revolves around determining the concentration of ions in a chemical reaction involving KOH and HBr, specifically focusing on the net ionic equation and the implications of stoichiometry and water autodissociation. Participants explore the relationship between the concentrations of reactants and products in a theoretical context, as well as the implications for a second-order rate reaction.

Discussion Character

  • Exploratory
  • Technical explanation
  • Debate/contested
  • Mathematical reasoning

Main Points Raised

  • One participant asks how to determine the concentration of ions from a balanced chemical reaction involving KOH and HBr.
  • Another suggests using stoichiometry and the concept of limiting reagents along with water autodissociation to find the concentration of ions.
  • A later post reiterates the need to find the limiting reagent to determine the concentration of H2O and subsequently the concentration of OH-.
  • Some participants clarify that the concentration of H2O is nearly constant and emphasize the importance of identifying any excess H+ or OH- ions.
  • One participant presents a specific experimental scenario involving equal volumes and concentrations of KOH and HBr, seeking to find the initial concentration of H+ for a rate reaction.
  • Another participant challenges the validity of the experiment, arguing that KOH and HBr in solution primarily consist of K+, OH-, H+, and Br- ions, and that the reaction occurs almost instantaneously.
  • Further clarification is sought regarding the implications of mixing KOH and HBr and the nature of the net ionic reaction.

Areas of Agreement / Disagreement

Participants express differing views on the experimental validity of determining ion concentrations from the reaction of KOH and HBr, with some emphasizing the instantaneous nature of the reaction while others focus on the stoichiometric calculations. No consensus is reached on the best approach to determine the initial concentration of H+.

Contextual Notes

There are unresolved assumptions regarding the nature of the solutions and the instantaneous reaction dynamics. The discussion also reflects varying interpretations of stoichiometric relationships and the implications of water autodissociation.

Plutonium88
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Please post this type of questions in HW section using the template.
If I have a balanced chemical reactoin, for example

KOH + HBr ==> H2O + KBr

And I am given the concentration and volume of both KOH and HBr, how is it possible to determine the concentration of one of the ions from the net ionic equation?

H + OH ==> H2O
 
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In this particular case you will need to combine stoichiometry (hint: limiting reagent) with water autodissociation (water ion product).
 
Borek said:
In this particular case you will need to combine stoichiometry (hint: limiting reagent) with water autodissociation (water ion product).

Sorry for placing this in the wrong thread.

So basically find the limiting reagent between KOH And KBR, to determine the concentration of H2O from that, and then using H2O to find the concentration of OH?

Then using the water autodissociation

Kw = 1*10^(-14)mol^2/L^2 (assuming room temperature)

where [OH][H] = Kw

[H] = Kw/[OH]
 
Plutonium88 said:
So basically find the limiting reagent between KOH And KBR, to determine the concentration of H2O from that, and then using H2O to find the concentration of OH?

No, concentration of H2O is (almost) constant. The only thing you need to check is the concentration of excess H+ or excess OH-. It may happen there is no excess of either - but then the problem is trivial.
 
I'm going to restate the question with the given information, can you tell me if I am on the right track?

In an experiment 0.5L of 0.020 mol/L of KOH is rapidly mixed with an equal volume of 0.020 mol/L of HBr. What is the initial concentration of H+.

I Specifically need the concentration of [H+] at t = 0 to solve a 2nd order rate reaction. For the rate reaction i am given the constant K and the value of the concentration [H+] at time t.

t = 1/k*(1/[H+]t - 1/[H+]0)So:

KOH + HBr = > H2O + Kbr

I am assuming that because KOH and HBr have the same concentrations and volumes that regardless of whether i use KOH or HBr to find the concentration of H2O i will get the same concentration.

[H2O] = 0.02 MOL KOH / L KOH * 1Mol H2O/1MolKOH
[H2O] = 0.02 MOL/L

From the net ionic equation

H+ + OH- = H2O

[H+] = [H2O] = 0.02 MOL/L

where this is the concentration at time t = 0
 
There is misconception here and there is no meaningful experiment for such a reaction to be done. "KOH" is merely a manner of speaking, in a solution called e is only K+ and OH-. KBr is same thing and HBr pretty nearly. Reaction of H+ with OH- that happens when you mix these solutions is orders of magnitude faster that. You con follow by ordinary means.
 
epenguin said:
There is misconception here and there is no meaningful experiment for such a reaction to be done. "KOH" is merely a manner of speaking, in a solution called e is only K+ and OH-. KBr is same thing and HBr pretty nearly. Reaction of H+ with OH- that happens when you mix these solutions is orders of magnitude faster that. You con follow by ordinary means.

I don't entirely understand what you are saying in the post. What I am taking from what you said is when you mix KOH and KBr the reaction of OH and H happens as a result, which can be shown from the net ionic equation right? What I'm trying to find though, is an initial concentration of H+ so that i can determine how long it takes for the concentration of H+ to decrease to a certain amount. And I'm presuming I have to find the initial concentration of H+ using the concentrations of KOH and KBr?
 
I am saying that when you mix these two things essentially all the chemical reaction that happens is the one you called net ionic reaction.
This is the fastest chemical reaction known, instantaneous equilibrium for ordinary purposes. So only thing limiting rate of concentration change in any part of your reaction vessel is speed of mixing.
 

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