Solving Stoichiometry Problem on Oxalate Mass Percent

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Discussion Overview

The discussion revolves around a stoichiometry problem related to determining the mass percent of oxalate in synthesized crystals through a redox titration involving permanganate ions. Participants explore the relationship between the moles of reactants at the equivalence point and the application of stoichiometry in the context of the balanced chemical equation.

Discussion Character

  • Debate/contested
  • Technical explanation
  • Conceptual clarification

Main Points Raised

  • One participant questions the necessity of using stoichiometry to convert moles of MnO4- to moles of oxalate, asserting that moles should be equal at the equivalence point in titrations.
  • Another participant challenges this view, stating that the concept of equal moles at the equivalence point is incorrect and emphasizes the need to consider the coefficients in the balanced chemical equation.
  • A later reply clarifies that the correct statement is that the number of equivalents of different species are equal at the equivalence point, highlighting the importance of the balanced equation.
  • Some participants note that previous experiences with simpler, 1:1 stoichiometry may have contributed to misunderstandings regarding more complex reactions.
  • There is a distinction made between acid/base titrations and redox titrations, with participants discussing the implications of this difference on the stoichiometric relationships.
  • One participant points out that the relationship between moles of acid and base is only valid for strong, monoprotic acids reacting with strong bases, and mentions the complexity introduced by polyprotic acids.

Areas of Agreement / Disagreement

Participants express disagreement regarding the interpretation of equivalence point relationships in titrations. There is no consensus on the application of the concept of equal moles, with some asserting it is incorrect in the context of the given redox reaction.

Contextual Notes

The discussion highlights the limitations of applying simple stoichiometric relationships without considering the specific balanced equation and the nature of the titration (redox vs. acid/base). Participants also acknowledge that prior learning experiences may have shaped their understanding of these concepts.

babbagee
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I am taking chemistry 1A again just to refresh my skills. The teacher was telling us how to figure out the mass composition of oxalate in some crystals that we had just synthesized. The equation is written below

2MnO4- + 5C2O42- + 16H+ ----> 2Mn2+ + 10CO2 + 8H2O

The question is to find the Mass percent of oxalate in the green crystals. The molarity of MnO4- that was used was .0432M, and the amount that was used was 11.57ml. The mass of the green crystals was .225g.

The teacher converted the Molarity to moles by multiplying it by .01157L. He then converted the moles of MnO4- to the moles of oxalate using the formula mentioned aboce.

My question is since this is a titration don't the moles of the MnO4- added equal the moles of oxalate at the equivalce point. I don't understand why he used stoichometry to get the moles of oxalate. This is what i had learned in my previos class that the moles of acid or base added equals the moles of base being titrated at the equvialnce point. Isnt the fundamental concept of titration that the moles are equal at equivalance point. I may be missing something here so can some one explain it to me. And if my point of view is worng can some one tell me when that concept of "moles are equal at equivalnce point" is used.

Thanks
 
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Rajvirnijjar said:
I am taking chemistry 1A again just to refresh my skills. The teacher was telling us how to figure out the mass composition of oxalate in some crystals that we had just synthesized. The equation is written below

2MnO4- + 5C2O42- + 16H+ ----> 2Mn2+ + 10CO2 + 8H2O

The question is to find the Mass percent of oxalate in the green crystals. The molarity of MnO4- that was used was .0432M, and the amount that was used was 11.57ml. The mass of the green crystals was .225g.

The teacher converted the Molarity to moles by multiplying it by .01157L. He then converted the moles of MnO4- to the moles of oxalate using the formula mentioned aboce.

My question is since this is a titration don't the moles of the MnO4- added equal the moles of oxalate at the equivalce point. I don't understand why he used stoichometry to get the moles of oxalate. This is what i had learned in my previos class that the moles of acid or base added equals the moles of base being titrated at the equvialnce point.

If this is what they taught you before, they were wrong. However, I seriously doubt that any decent Chem teacher would teach the above wrong idea. I strongly suggest you revise the mole concept and understand the theory behind titrations before proceeding.

Isnt the fundamental concept of titration that the moles are equal at equivalance point.

Again, NO !

I may be missing something here so can some one explain it to me. And if my point of view is worng can some one tell me when that concept of "moles are equal at equivalnce point" is used.

This concept is never used .The correct statement is "the number of equivalents of the different species are equal at the equivalence point." In the above example, an equivalent of MnO4- has 2 moles and an equivalent of C2O42- has 5 moles.

You can NOT relate the number of moles of different species WITHOUT using the balanced chemical equation !
 
I think that was my problem, in the past i never had equations with different coefficients. Usually the equations were already balanced with every thing having a 1 to 1 ratio. I guess that is what messed me up. What you said at is what I meant to say.

Thanks
 
Would this be correct then, for example if you were doing a acid base titration

nbase added = nacid initially
[acid]Vacid=[base]Vbase


correct or no
What is the difference between this statement and the statement i made above.

Thanks
 
Last edited:
It is the same as the previous statement, and hence, is incorrect for the same reason.
 
This is not an acid/base titration. It is a redox titration.
 
Last edited:
shrumeo said:
This is not an acid/base titration. It is a redox titration.

So it is only true for acid and base reactions.
 
what is only true for acid/base titrations?
the relation you gave above?
that would only be true for strong, monoprotic acids (HCl, HNO3) reacting with a strong base (NaOH)
if the acid were di or triprotic (H3PO4, H2SO4) then there would be 2-3 inflection points in your titration curve
the pic at the bottom is an example
http://www.dartmouth.edu/~chemlab/techniques/titration.html
 

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