
Yu Xuan L. answered 07/18/23
Medical Student at Yale University specializing in chemistry
- pH before adding KOH
- at this point there is only water in equilibrium with HClO with is a weak acid. The balanced equation is as follow
- HClO + H2O -> H3O+ + ClO-
- Prepare ICE table (Initial, Change, Equilibrium)
- initial HClO concentration = 50mL / 1000mL * 0.220M = 0.011 moles HClO
- I: HClO = 0.011moles; H3O+ = 0; ClO- = 0
- C: HClO = -x; H3O+ = +x; ClO- = +x
- E: Ka HClO = 3.8 x 10-8 = (H3O+)( ClO-)/HClO = X2/(0.011-x)
- NOTE! this Ka value is found via google! if your give Ka is different, it will result in slightly different answers!
- assuming the change in HClO is negligible due to properties of being a weak acid & general simplicity of calculation
- Ka HClO = 3.8 x 10-8 = (H3O)( ClO- )/ HClO = X2/(0.011)
- x = H3O+ = ClO- = 1.8 x 10-5 = H+
- -log H+ = -log(1.8x 10-5) = pH = 4.7
- Given 25mL of KOH
- balanced equation as given
- HClO + KOH -> KClO- + H2O
- Prepare ICE table same as previous; note there are both HClO and KOH now
- I: HClO = 0.011moles (as previously calculated)
- KOH 25mL of KOH = 0.0055 moles = 25mL / 1000mL * 0.220M
- KClO- = 0
- C: HClO = 0.011 moles -0.0055; KOH = 0.0055 - 0.0055; KClO = 0 + 0.0055
- note KOH is a strong base so it will completely dissociate thus the change in moles will be equal to moles of KOH present
- E: HClO = 0.0055; KOH = 0; KClO- = 0.0055
- use Henderson Hasselbach equation to calculate the pH in this established buffer system as we have now identified dissociation constant, [A-] and [HA]
- pH = pKa + log ([A-] / [HA])
- pH = -log(3.8x10-8) + log ([KClO]- /[HClO])
- pH = -log(3.8x10-8) + log (0.0055/0.0055)
- pH = ~7.4
- This problem follows the same principle as previous, i will answer in less depth for sake of you working through similar problems
- 40mL of KOH = 0.0088 moles
- equilibrium moles of:
- HClO = 0.011 - 0.0088; KOH = 0.0088 - 0.0088; KClO- = 0+ 0.0088
- HClO = 0.0022
- KCLO- = 0.0088
- pH = 7.4 + log (0.0088/0.0022) = ~8
- 50mL of KOH; at this point we have reached the equivalence point of the titration and there are no acids of base remaining
- the only major species is the salt KClO that is also the conjugate base ClO-
- moles of KOH = (50mL * 0.220M) / 100mL (this is the volume of acid plus base for total volume at play) = 0.011 moles or 0.11M
- hydrolysis of the weak base
- ClO- + H2O -> HClO + OH-
- set up ice table
- initial: ClO = 0.11moles; rest are 0
- change ClO = 0.11moles -x; HClO = +x; OH- = +x
- equilibrium = Kb = Kw/Ka = 1x10-14/3.8x10-8 = 2.6 x 10.7= x2 / 0.11
- again assume change in ClO is negligible and solve for x
- Kw is a value to typically remember or know off the topic of your head; along with relationship between Ka, Kb, and Kw
- our x or change in HClO or OH- = 1.7*10-4
- -log OH- = pOH = -log (1.7*10-4) = ~3.8
- pH = 14-pOH = 10.2
- 60mL of KOH; we have far passed the equivalence point of the titration; so the excess strong base will entirely determine the pH at this point
- 60mL KOH; 0.22M * 0.06L = 0.0132moles
- 0.011moles of the KOH will be used to neutralize the HClO acid which leaves us with 0.0022 moles remaining
- 0.0022 moles / 0.11L (note this is the cumulative volume of 60mL + 50mL) = 0.02M of KOH
- the remaining KOH fully dissociates into OH- ions
- -log (0.02) = 1.7
- pH = 14-pOH = 12.3