Acid-Base Equilibria Chapter 16. The common ion effect is the shift in equilibrium caused by the addition of a compound having an ion in common with the.

Slides:



Advertisements
Similar presentations
Acid-Base Equilibria and Solubility Equilibria
Advertisements

AQUEOUS EQUILIBRIA AP Chapter 17.
Chapter 16: Aqueous Ionic Equilibria Common Ion Effect Buffer Solutions Titrations Solubility Precipitation Complex Ion Equilibria.
Acid-Base Equilibria Chapter 16. The common ion effect is the shift in equilibrium caused by the addition of a compound having an ion in common with the.
Applications of Aqueous Equilibria
Acid-Base Equilibria and Solubility Equilibria Chapter
Chapter 17 ACID-BASE EQUILIBRIA (Part I) 1Dr. Al-Saadi.
Copyright McGraw-Hill Chapter 17 Acid-Base Equilibria and Solubility Equilibria Insert picture from First page of chapter.
A CIDS AND B ASES II IB C HEMISTRY G R.12 Topic 18 1 Chem2_Dr. Dura.
Finding the Equivalence Point (calculation method) Strong Acid vs. Strong Base –100 % ionized! pH = 7 No equilibrium! Weak Acid vs. Strong Base –Acid is.
Procedure for calculating pH of a titration Volume of titrant needed is based on amount of analyte.
Ch. 16: Ionic Equilibria Buffer Solution An acid/base equilibrium system that is capable of maintaining a relatively constant pH even if a small amount.
CHM 112 Summer 2007 M. Prushan Acid-Base Equilibria and Solubility Equilibria Chapter 16.
Chapter 16: Applications of Aqueous Equilibria Renee Y. Becker Valencia Community College 1.
Acids and Bases Chapter 15. Acids Have a sour taste. Vinegar owes its taste to acetic acid. Citrus fruits contain citric acid. React with certain metals.
Chapter 19 More about ACID-BASES. Self-Ionization of Water Two water molecules produce a hydronium ion & a hydroxide ion by the transfer of a proton.
Acid-Base Equilibria and Solubility Equilibria Chapter 16 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Buffers and Acid/Base Titration. Common Ion Suppose we have a solution containing hydrofluoric acid (HF) and its salt sodium fluoride (NaF). Major species.
1 Acid-Base Equilibria and Solubility Equilibria Chapter 16 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Updates Assignment 06 is due Mon., March 12 (in class) Midterm 2 is Thurs., March 15 and will cover Chapters 16 & 17 –Huggins 10, 7-8pm –For conflicts:
Acid-Base Equilibria Chapter 16. The common ion effect is the shift in equilibrium caused by the addition of a compound having an ion in common with the.
Aqueous Equilibria Chapter 17 HW problems: 3, 5, 14, 15, 16, 23, 24, 27a, 28a, 31, 37, 43, 45, 51, 57.
Aqueous Equilibria. The __________________________ is the shift in equilibrium caused by the addition of a compound having an ion in common with the dissolved.
Buffers, Titrations, and Aqueous Equilibria. Common Ion Effect The shift in equilibrium that occurs because of the addition of an ion already involved.
Acid-Base and Solubility Equilibria Common-ion effect Buffer solutions Acid-base titration Solubility equilibria Complex ion formation Qualitative analysis.
Acid-Base Equilibria Chapter 16. The common ion effect is the shift in equilibrium caused by the addition of a compound having an ion in common with the.
Acid-Base Equilibria and Solubility Equilibria Chapter 16 Dr. Ali Bumajdad.
(equimolar amounts of acid and base have reacted)
Chapter 15 Applications of Aqueous Equilibria Addition of base: Normal human blood pH is 7.4 and has a narrow range of about +/- 0.2.
1 Acid-Base Equilibria and Solubility Equilibria Chapter 17 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Acid-Base Equilibria and Solubility Equilibria Chapter 16 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
1 Acid-Base Equilibria and Solubility Equilibria Chapter 16 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Chapter 14 Acids and Bases.
Chapter 17 Additional Aspects of Aqueous Equilibria Subhash Goel South GA State College Douglas, GA © 2012 Pearson Education, Inc.
Ch. 17 – Other Aspects of Equilibrium The concept of equilibrium may be used to describe the solubility of salts and the buffering action of a solution.
Chapter 17: Applications of Aqueous Equilibria By: Ms. Buroker.
Acid-Base Equilibria and Solubility Equilibria Chapter 16 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Acid-Base Equilibria and Solubility Equilibria Chapter 17 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Strong base neutralizes weak acid Strong acid neutralizes weak base.
Acid-Base Equilibria Chapter 16. The __________________is the shift in equilibrium caused by the addition of a compound having an __________in common.
Acid-Base Equilibria and Solubility Equilibria Chapter 16 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
pH = - log [H + ] or pH = - log [H 3 O + ] Example: If [H + ] = 1 X pH = - log 1 X pH = - (- 10) pH = 10  What would be the pH of a.
15 Acids and Bases Contents 15-1 The Bronsted-Lowry Definitions 15-2 The Ion Product of Water, Kw 15-3 The pH and Other “p” Scales 15-4 Concentrations.
Ch 17: Additional Aspects of Aqueous Equilibria Brown, LeMay Ch 17 AP Chemistry.
Buffers Made Easy. Common ion effect Common Ion: the presence of an ion which appears in both the acid (or base) and a salt in the solution Common ion.
Acid-Base Equilibria and Solubility Equilibria Chapter 16 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Acid-Base Equilibria and Solubility Equilibria Chapter 17 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Acid-Base Equilibria and Solubility Equilibria Chapter 16 Semester 2/2014 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction.
The common ion effect is the shift in equilibrium caused by the addition of a compound having an ion in common with one of the products.
Acids and Bases. Acid-Base Theory Acids Have a sour taste Can dissolve metals Acid in your stomach Produce H +1 in water.
University Chemistry Chapter 12: Acid-Base Equilibria and Solubility Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or.
Acid-Base Equilibria Chapter HF( aq ) + H 2 O( l ) H 3 O + ( aq ) + F - ( aq ) Addition of NaF will shift the equilibrium to the _______because.
Acid-Base Equilibria Chapter HF( aq ) + H 2 O( l ) H 3 O + ( aq ) + F - ( aq ) Addition of NaF will shift the equilibrium to the _______because.
Titrations In a titration a solution of accurately known concentration (titrant) is added gradually added to another solution of unknown concentration.
Acid-Base Equilibria and Solubility Equilibria
Acid-Base Equilibria Chapter 15.
Acid-Base Equilibria and Solubility Equilibria
Acid-Base Equilibria and Solubility Equilibria
Acid-Base Equilibria and Solubility Equilibria
NH4+ (aq) H+ (aq) + NH3 (aq)
Acid-Base Equilibria and Solubility Equilibria
Acid-Base Equilibria and Solubility Equilibria
Copyright © Cengage Learning. All rights reserved
Buffers Titrations and the Henderson Hasselbach Equation
Acid-Base Equilibria Chapter 15.
Acid-Base Equilibria and Solubility Equilibria
Acid-Base Equilibria and Solubility Equilibria
Acid-Base Equilibria and Solubility Equilibria
Aqueous Equilibria Chapter 17
Presentation transcript:

Acid-Base Equilibria Chapter 16

The common ion effect is the shift in equilibrium caused by the addition of a compound having an ion in common with the dissolved substance. The presence of a common ion suppresses the ionization of a weak acid or a weak base. Consider mixture of CH 3 COONa (strong electrolyte) and CH 3 COOH (weak acid). CH 3 COONa (s) Na + (aq) + CH 3 COO - (aq) CH 3 COOH (aq) H + (aq) + CH 3 COO - (aq) common ion 16.2

A buffer solution is a solution of: 1.A weak acid or a weak base and 2.The salt of the weak acid or weak base Both must be present! A buffer solution has the ability to resist changes in pH upon the addition of small amounts of either acid or base CH 3 COOH (aq) H + (aq) + CH 3 COO - (aq) Consider an equal molar mixture of CH 3 COOH and CH 3 COONa Adding more acid creates a shift left IF enough acetate ions are present

Which of the following are buffer systems? (a) KF/HF (b) KCl/HCl, (c) Na 2 CO 3 /NaHCO 3 (a) KF is a weak acid and F - is its conjugate base buffer solution (b) HCl is a strong acid not a buffer solution (c) CO 3 2- is a weak base and HCO 3 - is it conjugate acid buffer solution 16.3

What is the pH of a solution containing 0.30 M HCOOH and 0.52 M HCOOK? HCOOH (aq) H + (aq) + HCOO - (aq) Initial (M) Change (M) Equilibrium (M) x-x+x+x x x+x x x 16.2 Mixture of weak acid and conjugate base! K a for HCOOH = 1.8 x [H + ] [HCOO - ] K a = [HCOOH] x = X pH = 3.98

HCl H + + Cl - HCl + CH 3 COO - CH 3 COOH + Cl

pH= 9.18 Calculate the pH of the 0.30 M NH 3 /0.36 M NH 4 Cl buffer system. What is the pH after the addition of 20.0 mL of M NaOH to 80.0 mL of the buffer solution? NH 3 (aq) + H 2 O (l) NH 4 + (aq) + OH - (aq) Initial End x xx 16.3 [NH 4 + ] [OH - ] [NH 3 ] K b = Change- x + x = 1.8 X (.36 + x)(x) (.30 – x) 1.8 X = 1.8 X  0.36x 0.30 x = 1.5 X pOH = 4.82

pH = 9.20 Calculate the pH of the 0.30 M NH 3 /0.36 M NH 4 Cl buffer system. What is the pH after the addition of 20.0 mL of M NaOH to 80.0 mL of the buffer solution? NH 4 + (aq) + OH - (aq) H 2 O (l) + NH 3 (aq) start (M) end (M) final volume = 80.0 mL mL = 100 mL 16.3 NH M x L = mol /.1 L = 0.29 M OH x L = mol /.1 L = 0.01M NH M x = mol /.1 L = 0.24M K a = = 5.6 X [H + ] [NH 3 ] [NH 4 + ] = 5.6 X [H + ] [H + ] = 6.27 X

= 9.20 Calculate the pH of the 0.30 M NH 3 /0.36 M NH 4 Cl buffer system. What is the pH after the addition of 20.0 mL of M NaOH to 80.0 mL of the buffer solution? NH 4 + (aq) H + (aq) + NH 3 (aq) pH = pK a + log [NH 3 ] [NH 4 + ] pK a = 9.25 pH = log [0.30] [0.36] = 9.17 NH 4 + (aq) + OH - (aq) H 2 O (l) + NH 3 (aq) start (M) end (M) pH = log [0.25] [0.28] final volume = 80.0 mL mL = 100 mL 16.3

Titrations In a titration a solution of accurately known concentration is added gradually added to another solution of unknown concentration until the chemical reaction between the two solutions is complete. Equivalence point – the point at which the reaction is complete Indicator – substance that changes color at the endpoint (hopefully close to the equivalence point) Slowly add base to unknown acid UNTIL The indicator changes color (pink) 4.7

Strong Acid-Strong Base Titrations NaOH (aq) + HCl (aq) H 2 O (l) + NaCl (aq) OH - (aq) + H + (aq) H 2 O (l) % ionization! No equilibrium

Weak Acid-Strong Base Titrations CH 3 COOH (aq) + NaOH (aq) CH 3 COONa (aq) + H 2 O (l) CH 3 COOH (aq) + OH - (aq) CH 3 COO - (aq) + H 2 O (l) CH 3 COO - (aq) + H 2 O (l) OH - (aq) + CH 3 COOH (aq) At equivalence point (pH > 7): 16.4

Strong Acid-Weak Base Titrations HCl (aq) + NH 3 (aq) NH 4 Cl (aq) NH 4 + (aq) + H 2 O (l) NH 3 (aq) + H + (aq) At equivalence point (pH < 7): 16.4 H + (aq) + NH 3 (aq) NH 4 Cl (aq)

Acid-Base Indicators 16.5

pH 16.5

The titration curve of a strong acid with a strong base. 16.5

Which indicator(s) would you use for a titration of HNO 2 with KOH ? Weak acid titrated with strong base. At equivalence point, will have conjugate base of weak acid. At equivalence point, pH > 7 Use cresol red or phenolphthalein 16.5

Finding the Equivalence Point (calculation method) Strong Acid vs. Strong Base –100 % ionized! pH = 7 No equilibrium! Weak Acid vs. Strong Base –Acid is neutralized; Need K b for conjugate base equilibrium Strong Acid vs. Weak Base –Base is neutralized; Need K a for conjugate acid equilibrium Weak Acid vs. Weak Base –Depends on the strength of both; could be conjugate acid, conjugate base, or pH 7

Exactly 100 mL of 0.10 M HNO 2 are titrated with 100 mL of a 0.10 M NaOH solution. What is the pH at the equivalence point ? HNO 2 (aq) + OH - (aq) NO 2 - (aq) + H 2 O (l) start (moles) end (moles) NO 2 - (aq) + H 2 O (l) OH - (aq) + HNO 2 (aq) Initial (M) Change (M) Equilibrium (M) x-x+x+x x x+x xx [NO 2 - ] = = 0.05 M Final volume = 200 mL K b = [OH - ][HNO 2 ] [NO 2 - ] = x2x x = 2.2 x – x  0.05x  1.05 x = [OH - ] pOH = 5.98 pH = 14 – pOH = 8.02

Complex Ion Equilibria and Solubility A complex ion is an ion containing a central metal cation bonded to one or more molecules or ions. Co 2+ (aq) + 4Cl - (aq) CoCl 4 (aq) 2- Co(H 2 O) 6 2+ CoCl

Complex Ion Formation These are usually formed from a transition metal surrounded by ligands (polar molecules or negative ions). As a "rule of thumb" you place twice the number of ligands around an ion as the charge on the ion... example: the dark blue Cu(NH 3 ) 4 2+ (ammonia is used as a test for Cu 2+ ions), and Ag(NH 3 ) 2 +. Memorize the common ligands.

Common Ligands LigandsNames used in the ion H2OH2Oaqua NH 3 ammine OH-hydroxy Cl-chloro Br-bromo CN-cyano SCN-thiocyanato (bonded through sulphur) isothiocyanato (bonded through nitrogen)

Names Names: ligand first, then cation Examples: –tetraamminecopper(II) ion: Cu(NH 3 ) 4 2+ –diamminesilver(I) ion: Ag(NH 3 ) 2 +. –tetrahydroxyzinc(II) ion: Zn(OH) 4 2- The charge is the sum of the parts (2+) + 4(-1)= -2.

When Complexes Form Aluminum also forms complex ions as do some post transitions metals. Ex: Al(H 2 O) 6 3+ Transitional metals, such as Iron, Zinc and Chromium, can form complex ions. The odd complex ion, FeSCN 2+, shows up once in a while Acid-base reactions may change NH 3 into NH 4 + (or vice versa) which will alter its ability to act as a ligand. Visually, a precipitate may go back into solution as a complex ion is formed. For example, Cu 2+ + a little NH 4 OH will form the light blue precipitate, Cu(OH) 2. With excess ammonia, the complex, Cu(NH 3 ) 4 2+, forms. Keywords such as "excess" and "concentrated" of any solution may indicate complex ions. AgNO 3 + HCl forms the white precipitate, AgCl. With excess, concentrated HCl, the complex ion, AgCl 2 -, forms and the solution clears.

Coordination Number Total number of bonds from the ligands to the metal atom. Coordination numbers generally range between 2 and 12, with 4 (tetracoordinate) and 6 (hexacoordinate) being the most common.

Some Coordination Complexes molecular formula Lewis base/ligand Lewis aciddonor atom coordination number Ag(NH 3 ) 2 + NH 3 Ag + N2 [Zn(CN) 4 ] 2- CN-Zn 2+ C4 [Ni(CN) 4 ] 2- CN-Ni 2+ C4 [PtCl 6 ] 2- Cl-Pt 4+ Cl6 [Ni(NH 3 ) 6 ] 2+ NH 3 Ni 2+ N6