Ionic bond forms between metal and non-metal.
Na is a metal, and F is a nonmetal.
Na and F form ionic bond.
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.
The answer to this is 22, confirmed by gradpoint
NaOH reacts with CH3COOH in 1:1 molar ratio to produce CH3COONa
NaOH + CH3COOH → CH3COONa + H2O
Mol CH3COOH in 52.0mL of 0.35M solution = 52.0/1000*0.35 = 0.0182 mol CH3COOH
Mol NaOH in 19.0mL of 0.40M solution = 19.0/1000*0.40 = 0.0076 mol NaOH
These will react to produce 0.0076 mol CH3COONa and there will be 0.0182 - 0.0076 = 0.0106 mol CH3COOH remaining in solution unreacted . Total volume of solution = 52.0+19.0 = 71mL or 0.071L
Molarity of CH3COOH = 0.0106/0.071 = 0.1493M
CH3COONa = 0.0076 / 0.071 = 0.1070M
pKa acetic acid = - log Ka = -log 1.8*10^-5 = 4.74.
pH using Henderson - Hasselbalch equation:
pH = pKa + log ([salt]/[acid])
pH = 4.74 + log ( 0.1070/0.1493)
pH = 4.74 + log 0.717
pH = 4.74 + (-0.14)
pH = 4.60.
