J.R. S. answered 06/12/19
Ph.D. University Professor with 10+ years Tutoring Experience
C6H5COOH ==> C6H5COO- + H+
a) Ka = 6.4x10-5 = [C6H5COO-][H+]/[C6H5COOH] = (x)(x)/0.150 - x
If we assume that x is small relative to 0.150 M, we can neglect it and avoid using the quadratic:
6.45x10-5 = x2/0.150 and x2 = 9.675x10-6
x = [H+] = 3.11x10-3 M (this is only 2% of 0.150 M so out assumption was correct)
pH = -log [H+] = -log 3.11x10-3 = 2.51
Not sure how you arrived at a pH of 3.0 and got it correct. You should have included your workings. Also, since you are adding a base, the pH would have to go up, not down as you have concluded.
b) Addition of NaOH will react with the acid to reduce the concentration of C6H5COOH and increase the concentration of C6H5COO- thus forming a buffer. C6H5COOH + OH- ==> C6H5COO- + H2O
Initial moles acid = 0.1 L x 0.150 mol/L = 0.0150 moles
Final moles acid = 0.0150 moles - 0.001 moles = 0.014 moles
Final moles conjugate base (C6H5COO-) = 0.001 moles
Since no volume change, final [acid] = 0.014 mol/0.1L = 0.14 M and final [conj.base] = 0.001mol/0.1L = 0.01M
Using the Henderson Hasselbalch equation pH = pKa + log [conj.base]/[acid] we can solve for pH.
pKa = -log Ka = -log 6.4x10-5 = 4.19
pH = 4.19 + log (0.01/0.14) = 4.19 + log 0.0714
pH = 4.19 + (-1.15)
pH = 3.04