[PDF] We discussed strong acid-strong base titrations last semester



Previous PDF Next PDF







Experiment 6 Titration II – Acid Dissociation Constant

Figure 4 Titration curve of weak diprotic acid by NaOH(aq) Pre-Lab Notebook: Provide a title, purpose, CH3COOH / NaOH reaction, brief summary of the procedure, and table of reagents (NaOH and CH3COOH) UCCS Chem 106 Laboratory Manual Experiment 6



Acid-Base Titration Curves Using a pH Meter

1) hydrochloric acid, HCl(aq) with sodium hydroxide, NaOH(aq); 2) acetic acid, CH 3 COOH(aq) with sodium hydroxide, NaOH(aq) The recorded volume and pH values will generate titration curves that will be used to compare features of the strong acid curve versus the weak acid curve You will determine the equivalence point volume and pH for both



FINDING THE UNKNOWN MOLARITY OF ETHANOIC ACID IN VINEGAR

Through this equation, we can say that the molarity of NaOH and the molarity of CH3OON is equal since their ration is 1:1 Since the NaOH is a standard solution, it reacts with the Acetic Acid (CH3COOH) The formula to find the moles and the molarity: This means that 1M of NaOH means that there is 1 mole in the NaOH/L Tjia 3



We discussed strong acid-strong base titrations last semester

the NaOH so, how much NaOH was added? 0 013 L NaOH soln x 0 01 mol NaOH = 0 0013 mol NaOH 1 L NaOH soln one mole CH 3CO 2H consumed and one mole of CH 3CO 2– formed for every mole of OH– added CH 3CO 2H OH– CH 3CO 2– start 0 0025 0 0013 0 rxn – 0 0013 – 0 0013 + 0 0013 after rxn 0 0012 ~ 0 0 0013



E17 Acid Ionisation Constant of Acetic Acid from Titration

addition of some NaOH, the +curve is relatively flat where [H (aq)] is given by equation (2) Near the equivalence point, the pH rises sharply At the equivalence point, all of the CH 3 COOH has reacted and the solution contains CH 3 CO 2 The pH at this point is greater than 7 as the acetate ion is a weak base and undergoes hydrolysis



Acids and Bases - University of Sydney

• Common strong bases are: NaOH, KOH, Ca(OH)2, Ba(OH)2 Weak indicates an equilibrium exists between the ions and the undissociated compound in solution with, very often, the undissociated compound dominating The pH of this solution may only be calculated if the equilibrium constant, K, as well as the concentration of the starting material is



Buffer Solutions - Cal State LA We Are LA

6 Buffer Solutions ν Let’s go back to problem of adding HCl to buffer solution: ν We can use H-H eqn to make the calculations much easier [CH3COOH] = 0 100 + [HCl]added [CH3COO-] = 0 100 – [HCl]



Acid-Base Chemistry

3O+] in a 0 053 M NaOH solution Step 1: since NaOH is a strong base, dissociation is complete ∴ [OH-] = 0 053 M Step 2: Use K w to calculate [H 3O+] K w = [H 3 O +][OH-] = 1 0 x 10-14 [H 3 O +] = K w [OH-] = 1 0 x 10-14 0 053-13= 1 9 x 10 M

[PDF] dosage d'une base faible par un acide fort pdf

[PDF] dosage ch3cooh par naoh

[PDF] exercice corrigé acide base mpsi

[PDF] réaction acido basique exercice corrigé mpsi

[PDF] acier s235jr norme

[PDF] s275jr equivalent

[PDF] acier s185 caractéristiques

[PDF] caractéristiques acier s275jr

[PDF] acier s275 caractéristiques

[PDF] acier s500mc

[PDF] s275jr caractéristiques mécaniques

[PDF] acier s420mc

[PDF] informe de acoso escolar en primaria

[PDF] bullying pdf libro

[PDF] informe sobre el bullying escolar

139Titration

We discussed strong acid-strong base titrations last semester.

Say we titrate HCl with NaOH

At the beginning of the titration, the pH is determined be the concentraion of the acid. After the end point of the titration, the pH is determined by the concentration of the base.

At the end point of the tirtation what is the pH?

At the endpoint the moles of HCl = the moles of NaOH so all that is present is H

2O, Cl-, and Na+. So, the pH is 7.

But what is different if a weak acid is titrated with a strong base? Lets say we are titrating a solution of acetic acid, CH

3CO2H, with

sodium hydroxide, NaOH. the reaction is CH

3CO2H(aq) + OH-(aq) --> CH3CO2-(aq) + H2O(l)

The sample of acetic acid is 25 mL of a acetic acid solution. It will be titrated with NaOH.

What is the pH before any base has been added?

just an equilibrium problem... CH

3CO2HH+CH3CO2-

init0.10~00 change- x+ x+ x equilibrium0.10 - xxx

1401.8 x 10

-5 = x2 (0.10 - x) x = 0.0013 [H +] = 0.0013pH = 2.87

What is the pH of the solution at the end point?

At the endpoint mol of NaOH = mol CH

3CO2H. What is present in the solution?

Na +, and CH3CO2-, (the OH- consumed the H+) Na + is neither an acid nor a base, but acetate is a base! So the pH is not 7! We have a base equilibrium problem.

So, what is the concentration of the base?

How many moles of acetate are present?

One mole of acetic acid produce one mole of acetate; so,

0.025 L CH

3CO2H x 0.1 mol CH 3 CO

2 H = 0.0025 mol CH

3CO2H1 L soln

0.0025 mol CH

3CO2H x 1 mol CH 3 CO

2 H = 0.0025 mol CH

3CO2- 1 mol CH

3CO2- So, what volume is the acetate in? Not 25 mL you added a solution of NaOH. how much base did you add? 1 mol acid for 1 mol base

0.0025 mol CH

3CO2H x 1 mol NaOH = 0.0025 mol NaOH 1 mol CH

3CO2H

141where did the NaOH come from? a NaOH solution

0.0025 mol NaOH x 1 L of solution = 0.025 L NaOH 0.1 mol NaOH

so, total volume is total vol = vol acid + vol titrant vol = 0.025 L + 0.025 L = 0.050 L

So, the concentration is

0.0025 mol CH

3 CO

2 -

= 0.050 M

0.050 L

Now finally the equilibrium problem!

CH

3CO2-CH3CO2HOH-

init0.0500~0 change- x+ x+ x equilibrium0.050 - xxx K b = x2(0.050 - x) remember K w = KbKa10-14 = Kb(1.8 x 10-5) K b = 5.56 x 10-10

5.56 x 10

-10 = x2 (0.050 - x) small x approximation x

2 = 2.78 x 10-11

x = 5.27 x 10 -6 [OH -] = 5.27 x 10-6 so, [H [H +][OH-] = 10-14 142[H
+] = 10-14/(5.27 x 10-6) [H +] = 1.90 x 10-9 pH = 8.72 Say we stop the titration at 13 mL NaOH. What is the pH? What is in solution after 13 mL NaOH have been added?

Na, CH

3CO2-, and CH3CO2H

Hey, this is a buffer problem! Both the acid and it conjugate base are present!

What are the concentrations?

moles of CH

3CO2H?

Started with 0.0025 mol CH

3CO2H and some of it was consumed by

the NaOH so, how much NaOH was added?

0.013 L NaOH soln x 0.01 mol NaOH = 0.0013 mol NaOH 1 L NaOH soln

one mole CH3CO2H consumed and one mole of CH3CO2- formed for every mole of OH- added CH

3CO2HOH-CH3CO2-

start0.00250.00130 rxn- 0.0013- 0.0013+ 0.0013 after rxn0.0012~ 00.0013

143Two ways to solve this

use Henderson-Haasbalch pH = pK a + log(0.0013/0.0012) pH = 4.75 + log(1.08) pH = 4.74 + 0.0347 pH = 4.78solve as equilibrium CH

3CO2HCH3CO2-H+

I

0.0012/0.038 L0.0013/0.038 L~0

C - x+ x+ x E

0.0316 - x0.0342 + xx

K a = x(0.0342 + x)/(0.0316 - x) small x approximation

1.8 x 10

-5 = x(1.08) [H +] = 1.67 x 10-5 => pH = 4.78 notice that if we had gone exactly halfway to the endpoint, added

0.00125 mol OH

-, pH = pKa

What happens if excess base has been added?

Say 37 mL NaOH have been added; what is the pH?

what is in solution Na +, CH3CO2-, and OH- what are the concentrations of all these things

0.037 L NaOH x 0.10 mol NaOH = 0.0037 mol OH

- 1 L 144CH

3CO2H(aq) + OH-(aq)H

2O(l) + CH3CO2-(aq)CH

3CO2HOH-CH3CO2-

S 0.00250.00370

R -0.0025-0.0025+0.0025

AR 0.00000.00120.0025

0.0012 mol OH

- = OH-(0.025 L + 0.037 L)

0.0025 mol CH

3 CO

2 -

= CH3CO2- but Kb is 5.56 x 10-10 so OH- (0.025 L + 0.037 L) from acetate is very small.

At the endpoint acetate

produced only 10-6 M OH- So, pH is determined by the concentration of excess NaOH! 10 -14 = [H+][OH-] [H +] = 10-14/(0.0194) [H +] = 5.167 x 10-13 pH = 12.29

Prove weak base doesn't matterCH

3CO2(aq) + H2OCH

3CO2H(aq) + OH-(aq)CH

3CO2-CH3CO2HOH-

0.0025 mol/0.06200.0012/0.062

-x+x+x

0.0025/0.062 - xx0.0012/0.062 + x

1455.56 x 10

-10 =x (

0.0012/0.062 + x)(

0.0025/0.062 - x)small x approximation

5.56 x 10

-10 =x (

0.0012/0.062)(

0.0025/0.062)x = 1.1583 x 10

-9[OH -] = 0.0012/0.062 + 1.1582 x 10-9 [OH -] = 0.0193548387097 + 0.0000000011582[OH -] = 0.0193548398679

What do you think? Is the [OH

-] contribution from the acetate significant?

146Add 25 mL of a HCl solution to 20.0 mL of a NH

3 solution. This is a strong acid weak base titration. We assume that the strong acid reacts with the weak base completely; then we analyze that which remains in solution.

The reaction isNH

3(aq) + H+(aq)NH

4+(aq)NH

3H+NH4+

S0.0020 mol0.0025 mol0

R-0.0020-0.0020+0.0020

AR00.00050.0020

So, some strong acid and some weak acid remain in solution.NH

3(aq) + H+(aq)NH

4+(aq)Do we need to solve this equilibrium problem?

No, [H

+] = 0.0005/(0.045) = why....since there is so much H+ already present the ammonium ion does not ionize much.

The increase in [H

+] caused by the ammonium ion is 2.24 x 10-9 M.

2.24 x 10

-9 is insignificant as compared to the H+ already present.quotesdbs_dbs5.pdfusesText_9