Answer:
The protonated form is predominant when aspirin is absorbed more readily. The ratio of conjugate base to acid is 1 to 100.
Explanation:
Aspirin is more readily absorbed when it is protonated, that is when pH is lower than pKa (<em>more H⁺ available in the medium</em>). We can confirm this using Henderson-Hasselbalch equation for pH = 1.5:

When aspirin is absorbed more readily the ratio of conjugate base to acid is 1 to 100, being the acid the <em>predominant</em> form.
Compare the density of the object in question to the density of water. If its density is less than water, it will float. For example, oak floats because its density is 0.7 g/cm³. If the density of an object is greater than water, it will sink.
Answer:2,3 -dimethyl-2-butenr
Explanation:
Answer:
electrons move around the nucleus in fixed orbits of equal amounts of energy
Explanation:
Quantum Theory