Answer:
they all reacted the same
Explanation:
Your answer is Breaking chemical bonds. Hope this helps
Answer:
Option B, aspirin’s ester group provides greater digestibility to aspirin
Explanation:
Aspirin ester group has three parts
- carboxylic acid functional group (R-COOH)
- ester functional group (R-O-CO-R')
- aromatic group (benzene ring)
Aspirin is a weak acid and hence it cannot dissolve in water readily. The reaction of Aspirin ester group with water is as follows -
aspirin
(acetylsalicylic acid) + water → salicylic acid + acetic acid
(ethanoic acid)
Aspirin passes through the stomach and remains unchanged until it reaches the intestine where it hydrolyses ester to form the active compound.
actually the answer is C. 15.0 on ed
