1 / 28

Chapter 4

Chapter 4. Types of Chemical Reactions and Solution Stiochiometry. Preview. the contents of this chapter will introduce you to the following topics: Water, Nature of aqueous solutions, types of electrolytes, and dilution

rusti
Download Presentation

Chapter 4

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Chapter 4 Types of Chemical Reactions and Solution Stiochiometry

  2. Preview the contents of this chapter will introduce you to the following topics: • Water, Nature of aqueous solutions, types of electrolytes, and dilution • Types of chemical reactions: precipitation, acid base reactions and oxidation-reduction reaction • Stoichiometry of reactions and balancing the chemical equations

  3. 4.1 Water, the Common Solvent Water is one of the most important substances on earth: • Cooling – engine, nuclear power plants, and many. • Transportation …etc. Water dissolve many different substances, e.g. salts, sugar, and many other To understand this process, we need to consider the nature of water: • As molecule, is H2O • Shape is V-shape with angle 105o • Band type of each O – H is covalent band and polar [electrons are not equirdlntty shared] • Polarity is polar with +ve charges of hydrogen and -ve on oxygen. This Polarity of water gives it the greatest ability to dissolve compounds.

  4. 4.1 Water, the Common Solvent • This Polarity of water gives it the greatest ability to dissolve compounds. Figure 4.2 shows schematic ionic solid dissolving in water. This process is called "Hydration". Note: • The stronger the ion-water attraction, the higher the solubility. • Therefore, not all the solid have the same solubility [chapter 11].

  5. 4.1 Water, the Common Solvent Water also dissolve non-ionic substances e.g. alcohols – "polar" and compatible structure to water: "like – dissolve – like" Figure 4.3 many substances don't dissolve in water e.g. animal fats "non-polar"

  6. Solution Solvent Solute 4.2 The Nature of Aqueous Solutions: Strong and Weak Electrolytes & non–Electrolyte • Solution – composite of solute (substance to be dissolved) + Solvent (Major substance e.g. water). • Solute: • Solvent: • dissolves in water (or other “solvent”) • changes phase(if different from the solvent) • is present in lesser amount (if the same phase as the solvent) • retains its phase(if different from the solute) • is present in greater amount (if the same phase as the solute) H2O Soft drink (l) Sugar, CO2 Air(g) N2 O2, Ar, CH4 Pb Sn Soft Solder (s)

  7. nonelectrolyte weak electrolyte strong electrolyte 4.2 The Nature of Aqueous Solutions: Strong and Weak Electrolytes & non–Electrolyte • One major property for characterizing aqueous solutions is its "Electrical conductivity" or its ability to conduct an electric current. Three solutions are observed: non electrolytes, weak, electrolytes and strong electrolyte. figure 4.4 • The basis for conductivity properties of solutions was first correctly identified by Svante Arrhenius (1859 – 1927) An electrolyte is a substance that, when dissolved in water, results in a solution that can conduct electricity.

  8. H2O C6H12O6 (s) C6H12O6 (aq) H2O NaCl (s)Na+ (aq) + Cl- (aq) CH3COOHCH3COO- (aq) + H+ (aq) 4.2 The Nature of Aqueous Solutions: Strong and Weak Electrolytes & non–Electrolyte • Arrhenius postulated that the electric current depend directly on the number of ions present. Strong Electrolyte – 100% dissociation Weak Electrolyte – not completely dissociated Nonelectrolyte does not conduct electricity? No cations (+) and anions (-) in solution

  9. 4.3 The Composition of Solutions: To perform stoichiomctric calculations at any chemical reactions you must know two things: • The nature of the reaction – exact forms of chemical in solutions. • The amounts of chemicals – "concentration" concentration of a solution can be described in many different ways, % , molar, molal, mole. faction .. etc. We will consider here the unit "molar"(M) or molarity: "the method used to prepare molar solutions". Molarity (M) = moles of solute per volume of solution in liters:

  10. 4.3 The Composition of Solutions: Notes: • For ionic systems the solution prepared will contain the number of moles prepared but for ionic species its different story e.g. 1.0M NaCl contains 1.0 mole NaCl or more accurate 1.0 mole of Na+ and 1.0 mole of Cl-. • Molarity can be used to determine number of moles per certain volumes where: Moles = Liters of solution x Molarity. Example 4.3 Gives the concentration of each type of ion in the solutions of 0.50M Co(NO3)2 Example 4.4 Calculate the number of moles of Cl- ions in 1.75 L of 1.0x10-3M ZnCl2

  11. 4.3 The Composition of Solutions: Standard Solution: Solution used in chemical analysis. it has accurately known concentration Dilution: it is the procedure to get low concentrated solution (diluted) from a high concentrated one. Moles of solute after dilution = moles of solute before dilution. (M x V) after = (M x V) before. Example 4.7 What volume of 16 M sulfuric Acid must be used to prepare 1.5 L of a 0.10M H2sO4 solution?

  12. 4.4 Types of Solution Reactions Millions of possible chemical reaction needs system for grouping them into classes. The commonly used by chemists: • Precipitation reactions AgNO3(aq) + NaCl(aq)  AgCl(s) + NaNO3(aq) • Acid-base reactions NaOH(aq) + HCl(aq)  NaCl(aq) + H2O(l) • Oxidation-reduction reactions Fe2O3(s) + Al(s)  Fe(s) + Al2O3(s)

  13. precipitate Pb(NO3)2(aq) + 2NaI (aq) PbI2(s) + 2NaNO3(aq) Pb2+ + 2NO3- + 2Na+ + 2I- PbI2 (s) + 2Na+ + 2NO3- Pb2+ + 2I- PbI2 (s) PbI2 4.5 Precipitation Reactions Precipitate – insoluble solid that separates from solution molecular equation ionic equation net ionic equation Na+ and NO3- are spectator ions

  14. 4.5 Precipitation Reactions SimpleRulesfor Solubility of Aq. Solutions 1. Most nitrate (NO3) salts are soluble. 2. Most alkali (group 1A) salts and NH4+are soluble. 3. Most Cl, Br, and I salts are soluble(NOTAg+, Pb2+, Hg22+) • Most sulfate salts are soluble (Except BaSO4, PbSO4, HgSO4, CaSO4) • Most OH salts are only slightly soluble (Except NaOH, KOH are soluble) 6. Most S2, CO32, CrO42, PO43 salts are only slightly soluble, i.e., Not soluble. • Exercise 4.8: • Using the solubility rules in table 4.1, predict what will happen when the following pairs of solutions are mixed. • KNO3(aq) & BaCl2(aq) • Na2SO4(aq) & Pb(NO3)2(aq) • KOH(aq) & Fe(NO3)(aq)

  15. AgNO3 (aq) + NaCl (aq) AgCl (s) + NaNO3 (aq) Write the net ionic equation for the reaction of silver nitrate with sodium chloride. Ag+ + NO3- + Na+ + Cl- AgCl (s) + Na+ + NO3- Ag+ + Cl- AgCl (s) 4.6Describing Reactions in Solution Writing Net Ionic Equations • Write the balanced molecular equation. • Write the ionic equation showing the strong electrolytes • Determine precipitate from solubility rules • Cancel the spectator ions on both sides of the ionic equation

  16. 4.7 Stoichiometry of Precipitation Reactions The procedures for calculating quantities of reactants and products involved in chemical reaction. The following steps summarized the procedure: Step 1: Identify the present in the combined solution, and determine what reaction occurs. Step 2: write the balanced net ionic equation. Step 3: calculate the moles of reactants. Step 4: determine which reactant is limiting. Step 5: calculate the moles of product or product as required. Step 6: convert to grams or other units, as requires. Example 4.11 When aqueous solutions of Na2SO4 and Pb(NO3)2 are mixed, PbSO4 precipitates. Calculate the mass of PbSO4 formed when 1.25L of 0.0500M Pb(NO3)2 and 2.00L of 0.0250M Na2SO4 are mixed.

  17. 4.8 Acid – Base Reactions: Acids Have a sour taste. Taste of vinegar is due to acetic acid. Citrus fruits contain citric acid. React with certain metals to produce hydrogen gas. React with carbonates and bicarbonates to produce carbon dioxide gas Bases Have a bitter taste. Feel slippery. Many soaps contain bases.

  18. 4.8 Acid – Base Reactions: Arrhenius acid is a substance that produces H+ (H3O+) in water Arrhenius base is a substance that produces OH- in water

  19. A Brønsted acid must contain at least one ionizable proton! 4.8 Acid – Base Reactions: A Brønsted acid is a proton donor A Brønsted base is a proton acceptor base acid acid base

  20. acid + base salt + water HCl (aq) + NaOH (aq) NaCl (aq) + H2O H+ + Cl- + Na+ + OH- Na+ + Cl- + H2O H+ + OH- H2O 4.8 Acid – Base Reactions: They are also called neutralization reaction Describing Reactions in Solution

  21. x acid + y base salt + water 4.8 Acid – Base Reactions: They are also called neutralization reaction Main reaction is titration, the key terms are: Titrant - solution of known concentration used in titration Analyte - substance being analyzed Equivalence point - enough titrant added to react exactly with the analyte Endpoint - the indicator changes color so you can tell the equivalence point has been reached. The neutralization reaction calculation: a. Write the correct balanced acid–base reaction. b. Use the following equation: y. (M.V)acid = x. (M.V)base

  22. 4.8 Acid – Base Reactions: In atitration 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 (or near) the equivalence point Slowly add base to unknown acid UNTIL the indicator changes color 4.7

  23. 2Mg (s) + O2 (g) 2MgO (s) 2Mg 2Mg2+ + 4e- O2 + 4e- 2O2- 2Mg + O2 + 4e- 2Mg2+ + 2O2- + 4e- 2Mg + O2 2MgO 4.9 Oxidation-Reduction Reactions: (electron transfer reactions) Oxidation half-reaction (lose e-) Reduction half-reaction (gain e-)

  24. 4.9 Oxidation-Reduction Reactions:

  25. Oxidation numbers of the elements in the following ? 4.9 Oxidation-Reduction Reactions: Rules for Assigning Oxidation States 1. Oxidation state of an atom in an element = 0 2. Oxidation state of monatomic element ions = charge 3. Oxygen =-2 in covalent compounds (except in peroxides where it = -1) 4. H = +1 in covalent compounds 5. Fluorine = -1 in compounds 6. Sum of oxidation states = 0 in compounds Sum of oxidation states = charge of the ion IF7 F = -1 7x(-1) + ? = 0 I = +7

  26. 4.10 Balancing Oxidation – Reduction Equations Balancing by Half-Reaction Method (Acidic) 1. Write separate reduction, oxidation reactions 2. For each half-reaction: • Balance elements (except H, O) • Balance O using H2O • Balance H using H+ • Balance charge using electrons 3. If necessary, multiply by integer to equalize electron count 4. Add half-reactions 5. Check that elements and charges are balanced

  27. 4.10 Balancing Oxidation – Reduction Equations Half-Reaction Method - Balancing in Base 1. Balance as in acid. 2. Add OH- that equals H+ ions (both sides!) 3. Form water by combining H+, OH- 4. Check elements and charges for balance

  28. 4.10 Balancing Oxidation – Reduction Equations MnO4- + ClO2- → MnO2 + ClO4-

More Related