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.
<span>C + O2 → CO2
(8,376,726 tons) x (0.80) / (12.01078 g C/mol) x (1 mol CO2/ 1 mol C) x
(44.00964 g CO2/mol) = 24,555,054 tons CO2</span>
A low specific heat capacity
There are approximately 4 resonance structures that can be drawn for N205 (no N-N bond) (minimal formal charge).
Given: C3H8(g) + O2(g) ----> CO2 (g) + H2O (g)
Step : Put a 3 in front of CO2 (g) to balance C
=> C3H8(g) + O2(g) ----> 3CO2 + H2O to balance H
Step 2: Put a 4 in front of H2O
=> C3H8 (g) + O2(g) -----> 3CO2 (g) + 4H2O (g)
Step 3: Given that there are 3*2 + 4 = 10 O to the right side, put a 5 in front of O2 to balance O:
=> C3H8(g) + 5O2(g) -----> 3CO2(g) + 4H2O(g)
You can verify that the equation is balanced.
So, the answer is that the coefficient in front of O2 is 5.
