Correlating pka and pH with ionic forms (exercises)

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SUMMARY

The discussion centers on the molecule benzotriazole, which has a pKa of 8.2, not 12 as initially stated by a teacher. At a pH of 6, the prevailing form of benzotriazole is neutral, as the pH is below the pKa. The confusion arises from the misinterpretation of pKa values, particularly regarding the distinction between the neutral molecule and its conjugate acid. Ultimately, the correct answer to the exercise is d) none of the above, as the provided pKa of 12 is hypothetical and does not apply to benzotriazole.

PREREQUISITES
  • Understanding of pKa and its implications for acid-base chemistry
  • Familiarity with the structure and behavior of benzotriazole
  • Knowledge of Bronsted acid-base theory
  • Ability to interpret pH and its relationship to pKa
NEXT STEPS
  • Research the structural characteristics of benzotriazole and its protonation states
  • Learn about the implications of pKa values in acid-base equilibria
  • Study the differences between neutral molecules and their conjugate acids
  • Explore the concept of weak acids and bases in organic chemistry
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Chemistry students, educators, and professionals interested in organic chemistry, particularly those studying acid-base behavior and molecular structure.

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Please post this type of questions in the homework section, filling the template.
I have the following molecule: benzotriazole. It has pka=12. At pH=6 which form prevails?

a) neutral
b) anionic
c) cationic
d) none of the above.

I thought the correct answer was c) cationic: pH<pka, benzotriazole has basic functional groups (amines).
 

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I don't know where your figure of 12 comes from. Wikipedia quotes a value of 8.2. Moreover, this is the pKa of the neutral molecule, not the conjugate acid. Benzotriazole behaves very differently from ordinary amines:
"Moreover, the proton does not tightly bind to any of the nitrogen atoms, but rather migrates rapidly between positions 1 and 3. Therefore, the BTA can lose a proton to act as a weak acid (pKa = 8.2)[3][4] or accept a proton using the lone pair electrons located on its nitrogen atoms as a very weak Bronsted base (pKa < 0)." (https://en.wikipedia.org/wiki/Benzotriazole)
People sometimes talk about the "pKa of an amine" when they mean the pKa of its conjugate acid, but this is sloppy, and in this case actually incorrect.
 
mjc123 said:
I don't know where your figure of 12 comes from. Wikipedia quotes a value of 8.2. Moreover, this is the pKa of the neutral molecule, not the conjugate acid. Benzotriazole behaves very differently from ordinary amines:
"Moreover, the proton does not tightly bind to any of the nitrogen atoms, but rather migrates rapidly between positions 1 and 3. Therefore, the BTA can lose a proton to act as a weak acid (pKa = 8.2)[3][4] or accept a proton using the lone pair electrons located on its nitrogen atoms as a very weak Bronsted base (pKa < 0)." (https://en.wikipedia.org/wiki/Benzotriazole)
People sometimes talk about the "pKa of an amine" when they mean the pKa of its conjugate acid, but this is sloppy, and in this case actually incorrect.

No.12 was given by our teacher ( this exercise was in the previous exam)...it’s more like hypothetically speaking. They just want to test if we know which form that molecule is in at pH x.

So...I guess in this case the correct answer is d).
 
In the circumstances, there is no correct answer. I don't know what your teacher was thinking. If it was a normal amine with pKa of conjugate acid 12, it would be cationic. If it was the pKa of the neutral amine (but with the wrong value), the answer would be neutral.
 

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