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Ch 4 Types of Chemical Reactions and Solution Stoichiometry. AP Chemistry 2014-2015. Ch 3/4 Quiz T 9/16 Ch 3/4 Exam Th 9/18. 4.1 Water, the Common Solvent. Water has a high specific heat, high heat of vaporization, and high adhesive/cohesive forces
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Ch 4 Types of Chemical Reactions and Solution Stoichiometry AP Chemistry 2014-2015 Ch 3/4 Quiz T 9/16 Ch 3/4 Exam Th 9/18
4.1 Water, the Common Solvent • Water has a high specific heat, high heat of vaporization, and high adhesive/cohesive forces • The two O-H bonds in water are polar covalent (oxygen is more electronegative—partial negative charge on oxygen, partial positive charge on each hydrogen) • Bond angle =~105° (the two unshared electron pairs on oxygen are “space hogs”, squishing the bond angle from a tetrahedral 109.5 despite four areas of electron density)
4.1 Continued • Partially positive hydrogens are attracted to negative ions, partially negative oxygen is attracted to positive ions hydration
4.1 Continued • For ionic solids: when the hydration attraction are greater than the crystal lattice attractions, the compound is soluble • Water can also dissolve nonionic substances (ex. alcohols, sugars) if they exhibit polarity • Fats (generally all nonpolar substances) do not dissolve in water • “Like dissolves like”
4.2 The Nature of Aqueous Solutions: Strong and Weak Electrolytes • A solution is homogeneous mixture where a solute is dissolved in a solvent; if the solvent is water the solution is considered “aqueous” • Properties of aqueous solutions • Electrolytes are solutions that conduct an electric current • Strong electrolytes completely dissociate (ex. strong acids, strong bases, soluble salts) • Common strong acids: HCl, HBr, HI, HNO3, H2SO4, HClO4 • Common strong bases: oxides and hydroxides of group 1A and 2A metals (2A metal salts tend to be less soluble than 1A metal salts) • Weak electrolytes do not completely dissociate (only about 1% dissociation)—examples include acetic acid and ammonia
Aqueous Solutions Continued • Nonelectrolytes are solutions in which the solute dissolves but does not make ions. They cannot conduct electricity. Ex. pure water, sugar, alcohol, antifreeze, starch • Arrhenius—the extent to which a solution can conduct an electric current depends on the number of ions present
4.3 The Composition of Solutions • Molarity = moles of solute/liters of solution (ex. 0.75 M NaCl means that for every 1 L of solution there are 0.75 moles of NaCl present)
Exercise 4.1 Molarity I • Calculate the molarity of a solution prepared by dissolving 11.5 g of solid NaOH in enough water to make 1.50 L of solution. (answer = 0.192 M) 11.5 g / 40.00 g/mol = 0.288 molNaOH M = moles/volume = 0.283 moles / 1.50 L = 0.192 M
Exercise 4.2 Molarity II—ions • Calculate the concentration of the cobalt (II) ions and the nitrate ions in a 0.50 M solution of cobalt (II) nitrate. (answer = 0.50 M Co2+ and 1.0 M NO3-) 0.50 M Co(NO3)2 [Co2+] = [Co(NO3)2] = 0.50 M [NO3-] = 2[Co(NO3)2] = 1.00 M
Exercise 4.3 Moles and Molarity • Calculate the number of moles of Cl- ions in 1.75 L of 0.001 M ZnCl2. (answer = .0035 moles Cl-) = 0.0035 moles Cl- 1.75 L 0.0001 moles 2 moles Cl- 1 mole ZnCl2 1 L
Exercise 4.4 Volume and Molarity • Typical blood serum is about 0.14 M NaCl. What volume of blood contains 1.0 mg NaCl? (answer = 0.12 mL) 1 mole NaCl 1.0 mg NaCl 1 g NaCl 1 L 0.14 moles 1000 mg 58.44 g = 1.2 x 10-4 L
Standard Solutions • A standard solution is a solution whose concentration is accurately known. To prepare a solution of known concentration, weigh out the solid as accurately as possible and place it in a volumetric flask. Add enough just enough distilled water to dissolve the solid and then fill to the mark on the flask. Mix.
Exercise 4.5 Standard Solutions To analyze the alcohol content of a certain wine, a chemist needs 1.00 L of an aqueous 0.200 M potassium dichromate solution. How many grams of solid K2Cr2O7 are needed to make this solution? 1.00 L 0.200 moles 294.20 g • = 58.8 g K2Cr2O7 1 mole K2Cr2O7 1 L
Dilution • M1V1= M2V2 • Generally, you measure out the quantity of stock (concentration) solution that you calculate from the formula above, and place it in a volumetric flask (of the correct volume for your dilution). Next you fill the volumetric flask to the mark on the neck with distilled water until the meniscus is reached. Mix.
Exercise 4.6 Dilution What volume of 16 M sulfuric acid must be used to prepare 1.5 L of a 0.10 M sulfuric acid solution? (answer = 9.4 mL) • (16 M)(x L) = (0.10 M)(1.5 L) • x = 0.0094 L or 9.4 mL
4.4 Types of Chemical Reactions • Review terms: chemical reaction, balanced chemical equation, (s), (l), (g), (aq) • Not all reactions fall neatly into one category
4.5 Precipitation Reactions • The formation of a precipitate is the driving force for some chemical reactions. A precipitate is an insoluble solid that is formed when two aqueous solutions are mixed. We can separate the precipitate from solution by filtration in what is called gravimetric analysis.
You have to know the solubility rules • Most alkali metal salts and ammonium salts are soluble • Chloride, bromide, and iodide are soluble—except for Ag+, Hg22+, and Pb2+ • Nitrates, chlorates, perchlorates, and acetates are soluble • Sulfates are soluble—except for Ca2+, Sr2+, Ba2+, Ag+, Hg22+, and Pb2+ • Carbonates, phosphates, chromates, dichromates, sulfides, hydroxides, and oxides are insoluble—but the first rule (most alkali metal salts and ammonium salts are soluble) takes priority • It can be assumed that ionic compounds that dissolve in water are strong electrolytes.
Exercise 4.7 Solubility Rules Predict what will happen when the following pairs of solutions are mixed. • Potassium nitrate and barium chloride • Sodium sulfate and lead (II) nitrate • Potassium hydroxide and iron (II) nitrate 2 KNO3(aq) + BaCl2(aq) 2 KCl(aq) + Ba(NO3)2(aq) No reaction Na2SO4(aq) + Pb(NO3)2(aq) PbSO4(s) + 2 NaNO3(aq) Formation of a precipitate, lead (II) sulfate 2 KOH(aq) + Fe(NO3)2 (aq) 2 KNO3(aq) + Fe(OH)2(s) No reaction
4.6 Describing Reactions in Solution • Complete balanced equation—gives the overall reaction stoichiometry but does not specify which reactants/products ionize • Complete ionic equation—same as above but represents all strong electrolytes as ions • Net ionic equation—includes only the solution components undergoing a change; spectator ions are not included • There is always a conservation of charge in net ionic equations
Exercise 4.8 Three types of equations Aqueous potassium chloride is added to aqueous silver nitrate to form a silver chloride precipitate plus aqueous potassium nitrate. • Write the complete balanced equation: • Write the complete ionic equation: • Write the net ionic equation: KCl(aq) + AgNO3(aq) AgCl(s) + KNO3(aq) K+(aq) + Cl-(aq) + Ag+(aq) + NO3-(aq) AgCl(s) + K+(aq) + NO3-(aq) Cl-(aq) + Ag+(aq) AgCl(s)
4.7 Stoichiometry of Precipitation Reactions • Precipitation reactions form an insoluble salt; this salt is dried and its mass is obtained • We can use stoichiometry to determine the expected/needed quantities of each compound
Exercise 4.9 Precipitation Reaction Stoichiometry I • Calculate the mass of solid sodium chloride that must be added to 1.50 L of a 0.100 M silver nitrate solution to precipitate all of the silver ions in the form of AgCl. (answer = 8.77 g NaCl) • NaCl(aq) + AgNO3(aq) AgCl(s) + NaNO3(aq) • 1.50 L AgNO3 • 1 mole NaCl 0.100 moles AgNO3 • 58.44 g NaCl • = 8.77 g NaCl 1 mole AgNO3 • 1 mole NaCl • 1 L AgNO3
Exercise 4.10 Precipitation Reaction Stoichiometry II • When aqueous solutions of sodium sulfate and lead (II) nitrate are mixed, lead (II) sulfate precipitates. Calculate the mass of lead (II) sulfate formed when 1.25 L of 0.0500 M lead (II) nitrate and 2.00 L of 0.0250 M sodium sulfate are mixed. (answer = 15.2 g lead (II) sulfate) • Na2SO4(aq) + Pb(NO3)2(aq) PbSO4(s) + 2 NaNO3(aq) • 1 mole PbSO4 • 303.3 g PbSO4 • 1.25 L Pb(NO3)2 • 0.0500 moles Pb(NO3)2 • = 19.0 g PbSO4 • 1 mole Pb(NO3)2 • 1 L • 1 mole PbSO4 • 1 mole PbSO4 • 303.3 g PbSO4 • 2.00 L Na2SO4 • 0.0250 moles Na2SO4 • = 15.2 g PbSO4 • 1 mole Na2SO4 • 1 L • 1 mole PbSO4
4.8 Acid-Base Reactions • Acids are compounds that produce anions and hydronium ions (H3O+) when they react with water (you can also just say hydrogen ions, H+, though hydronium is technically more correct)—Arrhenius definition • Bases are compounds that produce cations and hydroxide ions when they react with water—Arrhenius definition • NH3 is therefore not an Arrhenius acid, but it IS a Bronsted-Lowry acid because it is a proton acceptor • In a neutralization reaction, an acid and a base in equimolar (really equinormal) quantities react to produce water and a salt. The salt may or may not be soluble.
Exercise 4.11 Neutralization • What volume of a 0.100 M HCl solution is needed to neutralize 25.0 mL of 0.350 M NaOH? (answer = 0.0875 L = 87.5 mL HCl) • HCl(aq) + NaOH(aq) H2O(l) + NaCl(aq) • In other words, HCl is monoprotic and NaOH is monobasic, so they react in a 1:1 ratio. M1V1 = M2V2 applies (not always true for polyprotic acids/polybasic bases). • (0.100 M HCl)(V1 mL) = (0.350 M NaOH)(25.0 mL) • V1 = 87.5 mL
Acid-Base Titrations • Volumetric analysis is a technique for determining the amount of a certain substance by doing a titration • Review terms: titrant, analyte, burette, indicator
The equivalence point occurs when the number of moles of hydroxide ions is equal to the number of moles of hydrogen (hydronium) ions—this term is also used in redox titrations • The end point is where you see a color change when using an indicator
Standardization is a procedure for establishing the exact concentration of a reagent—ex. you may prepare a solution to be 0.50 M but it might be “off”; standardization helps you to determine the true concentration
Exercise 4.12 Standardization • A student carries out an experiment to standardize a sodium hydroxide solution. To do this the student weighs out a 1.3009 g sample of potassium hydrogen phthalate (KHC8H4O4 abbreviated KHP, molar mass 204.22 g/mol, has one acidic hydrogen). The student dissolves the KHP in distilled water, adds phenolphthalein as an indicator, and titrates the resulting solution with the sodium hydroxide solution to the phenolphthalein endpoint. The difference between the final and initial burette readings is 41.20 mL. Calculate the concentration of the sodium hydroxide solution. (answer = 0.1546 M NaOH)
Exercise 4.12 Continued • KHP: mass = 1.3009 g molar mass = 204.22 g/mole • NaOH: volume = 41.20 mL molarity = ? KHP is monoprotic, so KHP and NaOH react in a 1:1 ratio. Moles KHP = moles NaOH Moles KHP = 1.3009 g / 204.22 g/mole = 0.00637 moles KHP Moles NaOH = volume * molarity = 0.04120 L * V = .4120V 0.00637 = 0.04120V V = 0.1546 M
4.9 Oxidation-Reduction Reactions • Terms to know • OIL RIG (oxidation is loss, reduction is gain, of electrons) • Oxidation is the loss of electrons, which increases charge (more positive) • Reduction is the gain of electrons, which decreases charge (more negative) • Oxidation number is the assigned charge on an atom • Oxidizing agents get reduced, reducing agents get oxidized—reduction and oxidation must be coupled
Rules for assigning oxidation states • Always zero for elements • The oxidation state of a monatomic ions is the same as its charge • Fluorine is always -1, oxygen is almost always -2 (exceptions—peroxides where it is -1, or OF2 where it is +2) • Hydrogen is almost always +1; metal hydrides are an exception, where it is -1 (in these situations, hydrogen is placed at the end of a chemical formula like LiH) • The sum of the oxidation states must be zero for a neutral compound; for polyatomic ions, the sum of the oxidation states must equal the charge on the polyatomic ion • It’s odd, but there can be non-integer oxidation states. Ex. Fe3O4 where the oxygens total -8, so iron’s charge must be +8/3 Fe+8/3
Exercise 4.13 Oxidation States Assign oxidation states to each atom in the following compounds/ions. CO2 SF6 NO3- C = S = N = O= F = O = +4 +6 +5 -2 -1 -2
Exercise 4.14 Oxidation and Reduction I For the following reaction, identify the atoms that are oxidized and reduced. 2 Al(s) + 3 I2(s) 2 AlI3(s) Now go back and identify the oxidizing and reducing agents. Aluminum: 0 +3, so aluminum was oxidized Iodine: 0 -1, so iodine was reduced Aluminum: reducing agent Iodine: oxidizing agent
Exercise 4.15 Oxidation and Reduction II The following reactions are associated with metallurgy. For each reaction, identify the atoms that are oxidized and reduced. Then identify the oxidizing and reducing agents. 2 PbS(s) +3 O2(g) 2 PbO(s) + 2 SO2(g) PbO(s) + CO(g) Pb(s) + CO2(g) Ox: S (-2 +4) Red: O (0 -2) Ox agent: oxygen Red agent: sulfur Ox: C (+2 +4) Red: Pb(+2 0) Ox agent: lead Red agent: carbon
4.10 Balancing Oxidation-Reduction Equations • Divide the equation into oxidation and reduction half reactions (OIL RIG) • Balance all elements besides hydrogen and oxygen • Balance oxygen by adding water to the appropriate side of the equation • Balance hydrogen by adding hydrogen ions to the appropriate side of the equation
4.10 Continued • Balance the charge by adding electrons • Multiply the half reactions to make the electrons equal for oxidation/reduction reactions • Cancel terms when you recombine the two half reactions • These rules are for acidic solutions; if this takes place in a basic solution, you have one more step. Neutralize any hydrogen ions by adding the same number of hydroxide ions to each side; check your water and cancel terms as necessary • Check
Sample problem 1 Balance the following equation using the half-reaction method (acidic): MnO4-(aq) + I-(aq) Mn2+(aq) + I2 (aq) Reduction: Oxidation: Combined: Mn: +7 +2; gained 5 electrons • 5 e- + MnO4- Mn2+ • + 2 H2O • 4 H+ + I: -1 0; each iodine atom lost 1 electron (2 total) 2 I- I2 • + 2 e- Need to multiply Mn equation by 2 and I equation by 5 to get 10 electrons transferred; the number of electrons lost in one equation must equal the number of electrons gained in the other equation
Sample Problem 1 Continued Manganese: 8 H+ + 10 e- + 2 MnO4- 2 Mn2+ + 4 H2O Iodine: 10 I- 5 I2 + 10e- Now, we add and cancel. In this equation, only the electrons will cancel. 8 H+ + 2 MnO4- + 10 I- 2 Mn2+ + 4 H2O + 5 I2 We would reduce if we could, but this equation is finished.
Sample problem 2 Balance the following equation using the half-reaction method (basic): Ag(s) + CN-(aq) + O2(g) Ag(CN)2-(aq) + H2O Reduction: Oxidation: Combined: O: 0 -2; gained 2 electrons on two atoms 4 H+ + O2 + 4 e- 2 H2O Ag: 0 +1; lost 1 electron Ag + 2 CN- Ag(CN)2- + e- 4 H+ + O2 + 2 Ag + 4 CN- 2 Ag(CN)2- + e- + 2 H2O This equation is only correct in acidic solution; let’s make it basic now
4 H+ + O2 + 2 Ag + 4 CN- 2 Ag(CN)2- + e- + 2 H2O To make this basic, we will add enough hydroxide ions to each side to neutralize the four hydrogen ions present on the products side. This will give us 4 OH- + 4 H+ + O2 + 2 Ag + 4 CN- 2 Ag(CN)2- + e- + 2 H2O + 4 OH- Which simplifies to 2 H2O + O2 + 2 Ag + 4 CN- 2 Ag(CN)2- + e- + 4 OH- Because we made four molecules of water on the reactants’ side and we had two molecules of water on the right, we have to cancel two molecules of water from each side.
Exercise 4.15 Balancing Half Reactions Potassium dichromate reacts with ethanol (C2H5OH) as follows: H+(aq) + Cr2O72-(aq) + C2H5OH(l) Cr3+(aq) + CO2(g) + H2O(l) Balance this equation using the half-reaction method. Cr: +6 +3 so 3 electrons are gained; 2 atoms present 14 H+ + 6e- + Cr2O72- 2 Cr3+ + 7 H2O C: -2 +4 so 6 electrons are lost; 2 atoms present 3 H2O + C2H5OH 2 CO2 + 12 e- + 12 H+ We have 6 electrons gained in one reaction and 12 electrons lost in the other. We can fix this by multiplying so that 12 electrons are transferred (x2 chromium equation)
14 H+ + 6 e-+ Cr2O72- 2 Cr3+ + 7 H2O 3 H2O + C2H5OH 2 CO2 + 12 e- + 12 H+ Becomes 28 H++ 12 e- + 2 Cr2O72- 4 Cr3+ + 14 H2O 3 H2O + C2H5OH 2 CO2 + 12 e- + 12 H+ Which we add to get 16 H+ + 2 Cr2O72-+ C2H5OH 4 Cr3+ + 11 H2O + 2 CO2