I ask this question because if acid anhydrides are always unstable in water then my interest, as a studierstudent of pharmacology, would be greatly diminished. Acid anhydrides are, in my books, at least, the result of a dehydrationdehydratation reaction between two carboxylic acids and hence their structures look like this:
Where R1 and R2 are organic substituents.
I ask this question because if acid anhydrides are always unstable in water then my interest, as a studier of pharmacology, would be greatly diminished. Acid anhydrides are, in my books, at least, the result of a dehydration reaction between two carboxylic acids and hence their structures look like this:
Where R1 and R2 are organic substituents.
I ask this question because if acid anhydrides are always unstable in water then my interest, as a student of pharmacology, would be greatly diminished. Acid anhydrides are, in my books, at least, the result of a dehydratation reaction between two carboxylic acids and hence their structures look like this:
Where R1 and R2 are organic substituents.
I ask this question because if acid anhydrides are always unstable in water then my interest, as a studier of pharmacology, would be greatly diminished. Acid anhydrides are, in my books, at least, the result of a dehydration reaction between two carboxylic acids and hence their structures look like this:
Where R1 and R2 are organic substituents.
I ask this question because if acid anhydrides are always unstable in water then my interest, as a studier of pharmacology, would be greatly diminished.
I ask this question because if acid anhydrides are always unstable in water then my interest, as a studier of pharmacology, would be greatly diminished. Acid anhydrides are, in my books, at least, the result of a dehydration reaction between two carboxylic acids and hence their structures look like this:
Where R1 and R2 are organic substituents.
