Help need titration curve for Arginine

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SUMMARY

The discussion centers on the titration curve of Arginine, specifically examining its behavior at low pH. It is established that Arginine, when in an acidic environment, typically gains one proton at the carboxyl group (COO-) and maintains a +2 charge. The terminal C(=NH)-NH2 group does not gain additional protons due to its amphoteric nature, supporting the conclusion that the nitrogen in this group is hindered from further protonation. The referenced resource from Michigan State University provides additional insights into the protonation behavior of Arginine.

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This discussion is beneficial for biochemists, chemistry students, and anyone studying amino acid behavior in different pH environments, particularly those focusing on protein structure and function.

Daemos
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I have a question

When you do a titration curve for Arginine and you start it off in the acid exteme (low pH) does it gain anymore Hydrogens other than the one that always bonds to the COO- group? (so does it gain more than a +2 charge)

To rephrase, do any of the other two Nitrogens (other than the one double bonded to the Carbon in the R-Group) gain additional hydrogens when it acts as a base.
 
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Yes, the formula should be written in low pH like that:

[tex]HOOC-CH(NH_3)^+-(CH_2)_3-NH_2^+-C(=NH)-NH_2[/tex]

I don't think that the terminal C(=NH)-NH2 group takes additional protons, since they seem to be amphoteric.

But I have found this http://www.cem.msu.edu/~reusch/VirtualText/proteins.htm, mentioning that the [itex]C=NH[/itex] group protonates instead to give the same 2+ charge, which is logical as the nitrogen I mentioned is somewhat hindered to react with proton.

I feel confident that the website will help you very much; I've liked it too.

Take care.
 
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thanks a lot for the info :)
 
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