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HW Set #3 24 pt CHE 120 DO ALL WORK ON A SEPARATE SHEET SHow woRK (No work, No c

ID: 497234 • Letter: H

Question

HW Set #3 24 pt CHE 120 DO ALL WORK ON A SEPARATE SHEET SHow woRK (No work, No credit use constant info in book or tables from class (4pt) 1. For the following hypothetical reaction that begins with only A and B, where, initially the concentrations of [A] 0.100 M the concentration of (Bl 0.200 M Arg) 2 B 3 ceo, 4 Day Ko 1.00 x 1002 What is the concentration of every species at equilibrium? (8pt) 2. A 200 mL solution of 0.100 M solution of HF is slowly mixed with 0.1 M NaOH. Determine the pH after addition of o ml of NaOH, 50 L of NaOH, 100 ml of aOH, 200 mL of NaOH, 250 mL of NaoH (8pt) 3. A 200 mL solution of 0.100 M solution of Ammonia, NH is slowly mixed with 0.100 M HCI. Determine the pH after addition of o mb of HCI, 50 ml of HCI, 1 mL of HCI, 200 mL of HCI, 250 mL of HCl (4pt) Describe in exact detail (including gram quantities and identity of species) how you would 4. create a 500 mL solution of buffer with a pH 8.0 20

Explanation / Answer

Q2.

First of all, volumes will change in every case (Volume of base + Volume of acid), therefore the molarity will change as well

M = moles / volume

pH = -log[H+]

a) HA -> H+ + A-

Ka = [H+][A-]/[HA]

a) no NaOH

Ka = [H+][A-]/[HA]

Assume [H+] = [A-] = x

[HA] = M – x

Substitute in Ka

Ka = [H+][A-]/[HA]

Ka = x*x/(M-x)

7.2*10^-4 = x*x/(0.1-x)

This is quadratic equation

x =0.00813

For pH

pH = -log(H+)

pH =-log(0.00813)

pH in a = 2.08990

b) 50 ml KOH

This is in a Buffer Region, a Buffer is formed (weak base and its conjugate)

Use Henderson-Hassebach equations!

NOTE that in this case [A-] < [HA]; Expect pH lower than pKa

pH = pKa + log (A-/HA)

initially

mmol of acid = MV = 200*0.1 = 20 mmol of acid

mmol of base = MV = 0.1*50 = 5 mmol of base

then, they neutralize and form conjugate base:

mmol of acid left = 20-5 = 15 mmol

mmol of conjguate left = 0 + 5 = 5

Get pKa

pKa = -log(Ka)

pKa = -log(7.2*10^-4) = 3.142

Apply equation

pH = pKa + log ([A-]/[HA]) =

pH = 3.142+ log (5/15) = 2.664

c) for 100 ml

This is in a Buffer Region, a Buffer is formed (weak base and its conjugate)

Use Henderson-Hassebach equations!

NOTE that in this case [A-] < [HA]; Expect pH lower than pKa

pH = pKa + log (A-/HA)

initially

mmol of acid = MV = 200*0.1 = 20 mmol of acid

mmol of base = MV = 0.1*100 = 10 mmol of base

then, they neutralize and form conjugate base:

mmol of acid left = 20-10 = 10 mmol

mmol of conjguate left = 0 + 10= 10

Get pKa

pKa = -log(Ka)

pKa = -log(7.2*10^-4) = 3.142

Apply equation

pH = pKa + log ([A-]/[HA]) =

pH = 3.142+ log (10/15) = 3.142

d) Addition of Same quantitie of Acid/Base

This will be Hydrolisis (equilibrium of acid-base) and the weak acid/base will form an equilibrium

We will need Kb

Ka*Kb = Kw

And Kw = 10^-14 always at 25°C for water so:

Kb = Kw/Ka = (10^-14)/(7.2*10^-4) = 1.388*10^-11

Now, proceed to calculate the equilibrium

H2O + A- <-> OH- + HA

Then K equilibrium is given as:

Kb = [HA][OH-]/[A-]

Assume [HA] = [OH-] = x

[A-] = M – x

Substitute in Kb

1.388*10^-11 = [x^2]/[M-x]

recalculate M:

mmol of conjugate = 20 mmol

Total V = V1+V2 = 200+200 = 400

[M] = 20 mmol/400 = 0.05 M

1.388*10^-11 = [x^2]/[0.05 -x]

x = 8.33*10^-7

[OH-] =8.33*10^-7

Get pOH

pOH = -log(OH-)

pOH = -log (8.33*10^-7) = 6.079

pH = 14-pOH = 14-6.079= 7.92

e) Addition of base

There will be finally an Excess of Base!

mol of acid < mol of base

Calculate pOH directly

[OH-] = M*V / Vt

mmol of acid = MV = 200*0.10 = 20

mmol of base = MV = 250*0.1 = 25

therefre,

mmol of strng base left = 25-20 = 5 mmol

Vtotal = 250+200 = 450 mL

[OH-] = 5/450 = 0.01111

pOH = -log(OH-)

pOH = -log(0.01111) = 1.954

pH = 14-pOH = 14-1.954= 12.046

pH = 12.046

For Q3.

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