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CHEMICAL RXNS IN AQUEOUS SOLNS (4.4) • Chem. Rxns are driven by energetic forces. • Precipitation (formation of solid is the driving force). • Acid-Base neutralization (formation of water is the driving force). • Oxidation-Redox (redox; transfer of electrons to reduce electrical potential is the driving force).

CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

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CHEMICAL RXNS IN AQUEOUS SOLNS (4.4). Chem. Rxns are driven by energetic forces. Precipitation (formation of solid is the driving force). Acid-Base neutralization (formation of water is the driving force). - PowerPoint PPT Presentation

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Page 1: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

• Chem. Rxns are driven by energetic forces.• Precipitation (formation of solid is the

driving force).• Acid-Base neutralization (formation of water

is the driving force).• Oxidation-Redox (redox; transfer of

electrons to reduce electrical potential is the driving force).

Page 2: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

PRECIPITATION (4.5, 4.7)

• The formation of a solid (precipitate) when two aqueous solutions are mixed; we say that the product cmp is insoluble or only slightly soluble in water.

• Sol. salt I (aq) + Sol. salt II (aq) Solid cmp (s)• Table 4.1 Solubility Rules for Salts in Water

(memorize)• Ion interchange or metathesis (switch

cation/anion partners)

Page 3: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

T4.1 SOLUBILITY RULES

1. Most nitrates are soluble2. Most salts with Grp 1A ions and NH4

+ are soluble.

3. Most salts with Cl-, Br-, I- are soluble EXCEPT those with Ag+, Pb2+, Hg2

2+

4. Most sulfates are soluble EXCEPT those with Ba2+, Pb2+, Hg2

2+, Ca2+.5. Most hydroxides are slightly soluble EXCEPT

the strong bases.6. Most sulfides, carbonates, chromates and

phosphates are slightly soluble.

Page 4: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

CHEMICAL EQUATION (4.6)

• Identify reactants, products, states of matter [g, s, aq, ℓ].

• Balance equation to conserve mass.

• Calculate quantitative or stoichiometric relationships between rxn participants (R or P) based on balanced chemical rxn.

Page 5: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

CHEMICAL EQUATION (2)

• Formula Equation: write all reactants and products as “neutral molecules”, show state of each.

• Complete Ionic Equation: write strong electrolytes as ions (aq).

• Net Ionic Equation: cancel out spectator ions.

Page 6: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

SOLUTION STOIOCHIOMETRY

• Typical stoichiometric calculation for reactions taking place in aq soln.

1. Write balanced net ionic eqn to identify the chem reaction

2. Calculate mols of known A from VA and MA

3. Calculate mols of unknown B, then VB

4. VA, MA #mol A #mol B VB if MA and MB are known

5. Determine LR after Step 1 if appropriate.

Page 7: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

STOICHIOMETRIC PROBLEMSProb 48, 50

Page 8: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

ACID + BASE RXNS

• Acids donate protons, i.e. provide H+(aq) or H3O+ (aq, hydronium) ions in water (Arrhenius).

• Polyprotic acids: sulfuric, phosphoric.

• Bases accept protons.

Page 9: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

ACID + BASE RXN: NEUTRALIZATION

• Acid + Base → Salt + Water

• SA + SB: HCl (aq) + NaOH(aq) → NaCl(aq) + H2O(ℓ)

– Net ionic: H+(aq) + OH-(aq) → H2O(ℓ)

• WA + SB: HF(aq) + KOH(aq) → KF(aq) + H2O(l)

– Net ionic: HF(aq) + OH-(aq) → F-(aq) H2O(ℓ)

• SA + WB: Problem 4.57c

Page 10: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

ACID-BASE TITRATION (volumetric analysis)

• Exptal technique for determining quantity of an unknown substance (analyte in beaker) by reacting a measured volume of it with another reactant (titrant in buret) of known concentration.

• This method works when the rxn is 100% complete (reaches equivalence pt) and that there is an indicator (color change, pH) that signals the rxn completion (endpoint).

Page 11: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

NEUTRALIZATION TITRATION

• Write the balanced acid (assume to be analyte) + base (use strong base) rxn for the titration.

• Use an indicator (e.g. phenolphthalein) that signals the equivalence point.

• The molarity and volume of the titrant (SB) must be known accurately.

• Fig 4.18

Page 12: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

NEUTRALIZATION TITRATION Prob 4.66, 64

Page 13: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

OXIDATION-REDUCTION REACTIONS

• A redox reaction involves the transfer of electrons between reactants

• Electrons gained by one species must equal electrons lost by another

• Oxidation states or numbers are assigned to atoms and they change in a redox rxn.

• Both oxidation and reduction must occur simultaneously.

2

Page 14: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

OXIDATION STATES OR NUMBERS (OX#)

• Actual or imaginary charge on atom: single atom, atom in molecule or atom in polyatomic ion

• We use these to keep track of electrons ub redox rxns.

• We will study rules for assigning OX# and then use this information to balance redox equations

Page 15: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

DETERMINING OX# (T4.2)

• OX# of an atom in an element is 0 [Fe, O2]

• If the species is neutral, sum of OX# is 0 [NaCl, SnO4]

• If the species is charged, sum of OX# is value of charge (NH4

+; SO42-)

• OX# of a monatomic ions is its charge: 1A atoms have OX# = +1; 2A atoms have OX# = +2; 7A atoms have OX# = -1, etc

Page 16: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

OX# (2)

• In molecular (covalent) cmps O has OX# = -2; sometimes -1 (with metal)

• In molecular (covalent) cmps H has OX# = +1; sometimes -1 (peroxide)

• F always has OX# = -1; other halides can have other OX#s

• There are exceptions

Page 17: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

OXIDATION

• If atom X in compound A loses electrons and becomes more positive (OX# increases), we say X (with charge) or A is oxidized.

• Also, we say that A is the reducing agent (RA) or is the electron donor.

Page 18: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

REDUCTION

• If atom Y in compound B gains electrons and becomes more negative (OX# decreases), we say Y (with charge) or B is reduced.

• Also, we say that B is the oxidizing agent (OA) or is the electron acceptor.

Page 19: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

ACTIVITY SERIES (Expt 7)

• Redox participants have varying capacities to gain or lose electrons.

• The Activity Series lists metal elements in order of decreasing strength as a reducing agent; ie. ability to lose electrons and undergo oxidation.

• A particular rxn in the list will cause the reduction of any rxn below it.

Page 20: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

Activity Series of Metals in Aqueous Solution

Page 21: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

INTERPRETATION OF ACTIVITY SERIES

• The strongest RA is at the top (Li) meaning that Li loses electrons and is oxidized. Therefore, the other metal must be reduced.

• When Lithium and Calcium react,

• 2Li(s) + Ca2+(aq) 2Li+(aq) + Ca(s)

• We say that Li displaces calcium ion from soln. Li(s) dissolves and Ca(s) forms

Page 22: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

BALANCING REDOX EQNS Half-Rxn Method (acid)

• Write half chem eqn for reduction

• Write half chem eqn for oxidation

• Balance all atoms except H and O

• Balance O with H2O and H with H+

Page 23: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

Half-Reaction Method (acid, 2)

• Add electrons to balance charge (I.e. show loss or gain of electrons)

• Balance the number of electrons between the two half-rxns by multipying by appropriate factor (i.e. #e- gained by by atom Y = #e- lost by atom X)

• Add two half-rxns and cancel identical species.

• Check for atom and charge balance

Page 24: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

The Half-Reaction Method (Acidic Solution)

Page 25: CHEMICAL RXNS IN AQUEOUS SOLNS (4.4)

Half-Reaction Method (base)

• Follow steps for acidic solution

• Add OH- ions to cancel out the H+ ions, thus forming water.

• Cancel out water molecules

• Check for atom and charge balance. Make sure there are no H+ ions remaining.