MadSci Network: Chemistry |
I have a students who is comparing ascorbic acid and citric acid as pH modifiers in an experiment to look at denaturing of the bromelain enzyme in pineapple. On consideration of the structure of ascorbic acid to explain its effect I see it has no carboxyl group only hydroxyl groups and a carbonyl group. Does the carbonyl group on an adjacent carbon sufficiently withdraw and delocalise electrons to cause the dissociation of the hydroxyl group on the next carbon atom to cause the acidity of ascorbic acid?
Re: Why is ascorbic acid an acid if it has no COOH group?
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