@atzirib33 Good catch! Going by the carboxyl group’s pKa, it would be protonated at a pH of ~2 or below. For the sake of specificity, I’ve edited the suggestion to include this
@atzirib33 Good catch! Going by the carboxyl group’s pKa, it would be protonated at a pH of ~2 or below. For the sake of specificity, I’ve edited the suggestion to include this