Titration of HBrO: Calculating pH of KOH Volumes

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SUMMARY

The discussion focuses on the titration of 20.0 mL of 0.100 M HBrO with 0.200 M KOH, calculating pH at various volumes of KOH. The calculated pH values are 4.80 for 0.00 mL, 8.50 for 5.00 mL, 10.72 for 10.00 mL, and 12.90 for 30.00 mL after correcting for excess hydroxide concentration. The participant initially miscalculated the pH for the final volume due to misunderstanding the influence of excess hydroxide ions beyond the equivalence point. The correct approach involves calculating the concentration of excess OH- to determine the final pH accurately.

PREREQUISITES
  • Understanding of weak acids and their dissociation constants (Ka) such as HBrO (Ka=2.5x10-9)
  • Knowledge of titration concepts and equivalence points in acid-base reactions
  • Familiarity with the Henderson-Hasselbalch equation for pH calculations
  • Basic skills in stoichiometry and ICE (Initial, Change, Equilibrium) tables
NEXT STEPS
  • Learn about the Henderson-Hasselbalch equation for buffer solutions
  • Study the calculation of pH at equivalence points in titrations
  • Explore the concept of titration curves and their significance in acid-base chemistry
  • Investigate the effects of concentration changes on pH in titration scenarios
USEFUL FOR

Chemistry students, educators, and anyone involved in laboratory work related to acid-base titrations and pH calculations.

osker246
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Homework Statement


Consider the titration of 20.0mL of a 0.100 M solution of HBrO, a weak acid (Ka=2.5x10-9) with 0.200 M KOH. Calculate the pH of the following volumes of KOH.

a. 0.00mL
b. 5.00mL
c. 10.00mL
d. 30.00mL



Homework Equations


pH=pKa +log [base]/[acid]


The Attempt at a Solution



Im having trouble with C when the pH is at its equivalance point.

so,

10.00mL (.200 mmol KOH/mL) = 2.00 mmol OH-

So stoichiometricaly my OH- and HBrO are used to completely to give me a conjugate base of 2.00 mmol BrO-

[BrO-]=2.00mmol/30.00ml=.0667 M

I set up my ice chart:

BrO-<=====>OH-+HBrO
I .0667 0 0
C -x +x +x
E .0667-x x x


Where

Kb=[OH-][HBrO]/[BrO-]=x2/.0667-x=4.0x10-6

Assume x is small to find x=[OH-]=5.2x10-4

pOH=3.28
pH= 14-pOH=10.72

What doesn't make sense to me is in Part A pH=4.80, part B pH=8.5, Part C=10.72 and part D pH=8.20.

Now shouldn't the pH in part D be greater than part C since I have excess OH-?

I'll type of my work for Part D in a bit. I have to leave right now. But if somebody can help my checking my answers I'd appreciate it. Thanks.
 
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When your solution is far past the endpoint, the pH only depends on the excess hydroxide. How much or what is the concentration of the excess hydroxide? This helps to give you your pH calculation. pH + pOH = 14.
 
Ohhhhhhhh!

I see what I forgot to do. I knew that once past the end point the only thing affecting pH was excess hydroxides. I just forgot to properly calculate the concentration. I tried using the henderson-hassalbach(sp?) equation instead. So since I have an excess of 4.00 mmol of hydroxide and a total volume of 50.00mL, [OH-]=.0800 M. So leaving me with a final pH of 12.903 for part D. Thank you very much!
 

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