A 1.00 L buffer solution is 0.150 M in HC_7H_5O_2 and 0.250 M in LiC_7H_5O_2. How do you calculate the pH of the solution after the addition of 100.0 mL of 1.00 M HCl? The Ka for HC_7H_5O_2 is 6.5 × 10^–5.

1 Answer
Apr 11, 2016

You can do it like this:

Explanation:

It looks like the acid is benzoic acid C_6H_5COOH

For short - hand I'll call this HA

Benzoic acid dissociates:

HA_((aq))rightleftharpoonsH_((aq))^(+)+A_((aq))^-" "color(red)((1))

The lithium salt provides a large reserve of the co - base A^- by dissociating completely:

LiA_((s))rarrLi_((aq))^(+)+A_((aq))^-" "color(red)((2))

The initial no. moles of A^- is given by:

nA_("init")^(-)=1xx0.25=0.25

The no. H^+ added is given by:

nH^(+)=1xx100/1000=0.1

From color(red)((1)) you can see that these H^+ ions will be absorbed by the large reserve of A^- ions shifting the equilibrium to the left thus "buffering" the pH.

You can see that they react in a 1:1 molar ratio so that the no. of moles of A^- remaining is given by:

nA^(-)=0.25-0.1=0.15

Each mole of H^+ added will form 1 mole of HA so no. moles HA formed =0.1

The initial moles of HA is given by:

nHA_("init") = 0.15xx1 =0.15

So the total moles HA is given by:

nHA=0.1+0.15=0.25

The expression for the acid dissociation constant K_a is given by:

K_a=([H_((aq))^(+)][A_((aq))^-])/([HA_((aq))])

Rearranging:

[H_((aq))^+]=K_axx([HA_((aq))])/([A_((aq))^-])

I will ignore any changes in concentration due to the dissociation of the acid as it is very small.

The total volume is common to both acid and co - base and will cancel so we can write:

[H_((aq))^+]=6.5xx10^(-5)xx0.25/0.15=1.083xx10^(-4)

pH=-log(1.083xx10^(-4))

color(red)(pH=3.96)