Reactions - luckyscienceluckyscience.com/AP chem/Powerpoints/Reactions.pdf(Bronsted-Lowry definition...

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Reactions So Many Reactions Such Little Time

Transcript of Reactions - luckyscienceluckyscience.com/AP chem/Powerpoints/Reactions.pdf(Bronsted-Lowry definition...

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Reactions

So Many Reactions Such Little Time

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Same as Before, But Different

• Name types of reactions – In “regular chemistry”

• Single Replacement • Double Replacement • Composition, Synthesis • Decomposition • Combustion

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Solubility Rules for Common Ionic Compounds in Water

You need to memorize solubility rules. 1. Most nitrates are soluble. 2. Most salts containing alkali metal ions and ammonium are soluble

Li+1, Na+1, K+1, Cs+1, NH4+1

3. Most chloride, bromide, and iodide salts are soluble Notable exceptions are Hg2

+2, Ag+2, Pb+2

4. Most sulfate (SO4) salts are soluble Notable exceptions are Ca +2, Ba+2, Pb+2, Hg2

+2

5. Most hydroxides are only slightly soluble. Na+ and K+are soluble. Ba +2, Sr +2 and Ca +2 are marginally soluble

6. Most sulfide (S-2), carbonate (CO3-2), chromate (CrO4

-2) and phosphate (PO4

-3) are only slightly soluble.

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Thank’s Luck for the Handout

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Reactions in Solution • KOH(aq) + Fe(NO3)3(aq) → Fe(OH)3(s) +3KNO3(aq) • Aq = aqueous or soluble in water. • S = solid or insoluble, it is the precipitate.

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How do you write equations? Molecular Equations • 3KOH(aq) + Fe(NO3)3(aq) → Fe(OH)3(s) ↓ + 3KNO3(aq) • Complete Ionic Equations • 3K+1

(aq)+ 3OH-1(aq) + Fe+3

(aq) + 3NO3-1

(aq) → Fe(OH)3(s) + 3K+1(aq) + 3NO3

-1(aq)

You do not need the (aq) it is understood. • Net Ionic Equations (Use this form on AP Exam) • 3OH-1

(aq) + Fe+3(aq) → Fe(OH)3(s)

• Spectator ions do not react (change) • Not included in the Net Ionic Equation

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Write the Net Ionic Equation • Get out your periodic table Steps to write Net Ionic Equations • Determine the reaction • Evaluate the spectators • Write the equation

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Write the Net Ionic Equation All Precipitate Reactions

• NH4Cl + AgNO3 →

• Na2S + CuSO4 →

• KOH + FeCl2 →

Ag+1 + Cl-1 → AgCl

Cu+2 + S-2 → CuS

Ag+1 + Cl-1 → AgCl

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Net Ionic Equations Acid base Reactions

• Acid donates a proton (H+1) and Base accepts a proton. (Bronsted-Lowry definition of an acid)

H+1(aq) + OH –1

(aq) → H2O(l)

• Strong acids are highly dissociated HCl is written H+ + Cl- (assuming both ions react!)

• Weak acids are “associated” Acetic Acid is written HC2H3O2 ,

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How do you know an acid is strong or weak?

• You have memorized the strong acids – H2SO4

– HCl, HBr, HI – HClO4

– HNO3 • All the other acids are weak electrolytes

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Common Misconceptions

• All weak acids are not soluble in water – Acid solubility is not related to solubility – It has to do with the basicity of the conjugate

base • Weak acids are dilute solutions

– Concentration is not related to acid strength – There can be 98 % solutions of sulfuric and

acetic acid

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Net Ionic Equations Acid base Reactions

Acetic acid is reacted with a solution of potassium hydroxide • Molecular equation:

– KOH + HC2H3O2 → H2O + K C2H3O2

• Net Ionic Equation – OH-1 + HC2H3O2 (l) → H2O(l) + C2H3O2

-1 • Why is Acetic acid written out?

– It is a weak electrolyte, so it exists as HC2H3O2 (l) – KOH is a strong electrolyte, it is completely ionized.

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Redox reactions

• Many chemical reactions involve a transfer of electrons between some of the atoms in a reaction. These are called redox reactions.

• The reactions must be properly balanced, so that there is no net gain or loss of electrons.

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Introduction to Redox Reactions

• Oxidation is the loss of electrons. Oxidized: atom, molecule, or ion becomes more positively charged.

• Reduction is the gain of electrons

Reduced: atom, molecule, or ion becomes less positively charged.

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Memory Devices –Oxidation or Reduction???

–LEO the lion goes GER – Lose Electrons Oxidation – Gain Electrons Reduction –OIL RIG – Oxidation Is Loss – Reduction Is Gain

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Balancing a Molecular Redox Equation

• Assign oxidation numbers to determine which substance(s) are oxidized and which are reduced.

•Cu + HNO3 → Cu(NO3)2 + H2O + NO

•Adjust coefficients to balance the atoms of the elements that are being oxidized and reduced. •Adjust the coefficients of the oxidized and reduced substances so that the total # electrons lost equals the total # electrons gained. •Adjust coefficients to balance the atoms of all other elements by inspection.

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KMnO4 Redox Molecular Equation • Now you try it! •KMnO4(aq) + Fe(NH4)2(SO4)2•6H2O(aq) + H2SO4 (aq)

•MnSO4(aq) + Fe2(SO4)3(aq) + K2SO4(aq) + (NH4)2SO4(aq) + H2O(l)

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Steps for Balancing Ionic Redox Reactions

• Write the net ionic equation with the oxidation numbers.

• Break equation apart into half-reactions. • Change coefficients to balance elements other

than oxygen or hydrogen • Balance oxygen by adding H2O • Balance hydrogen by adding H+

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Steps for Balancing Ionic Redox Reactions

• Balance electric charge on both sides by adding electrons

• Multiply each half-reaction by some number to make number of electrons transferred equal

• Combine half-reactions and cancel • If in basic solution, add one OH- to each side for

each H+ and simplify water.

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Balance an Ionic Redox Equation • Cr2O7

2- + Cl1- → (acidic solution)

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Balance an Ionic Redox Equation • Cr2O7

2- + Cl1- → (basic solution)

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Balance an Ionic Redox Equation • CH3OH + MnO4

1- → (acidic soln)

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Synthesis Reactions • Find an example of each type in your packet - • a. metal + nonmetal → binary salt • b. metal + oxygen → metal oxide • c. nonmetal + oxygen → nonmetal oxide • d. metal oxide + nonmetal oxide → ternary salt • e. metal oxide + water → base • f. nonmetal oxide + water → oxyacid • g. ammonia + acid → ammonium salt

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Decomposition

a. binary salt or binary oxide → elements b. metal carbonates → metal oxide + carbon dioxide c. metal hydrogen carbonates → metal oxide +

carbon dioxide + water d. metal hydroxide → metal oxide + water e. oxyacids → nonmetal oxide + water f. metal chlorates → salt + oxygen

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Single Replacement and Redox

a. metal replaces metal b. metal replaces H from water or acid c. halogen replaces halide d. An oxidizing agent in presence acid (or base)

forms water, oxidizes whatever else is in solution and the reduced products (know products from classic oxidizing agents)

Use activity series

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Single Replacement Reactions

• Remember the Activity Series! 3Na + AlCl3(aq) → Al + 3NaCl(aq)

Al + 3NaCl(aq) → 3Na + AlCl3(aq) Which one occurs for real? Why?

Li K Ba Sr Ca Na Mg Al Mn Zn Fe Cd Co Ni Sn Pb H Cu Ag Hg Au

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Single Replacement

• 2NaCl + F2 → 2NaF + Cl2 Or • 2Cl- + F2 → 2F- + Cl2

• The activity of the halides is in their order

on the periodic table

F Cl Br I

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Double Replacement

a. formation of a precipitate b. acid/base reaction

a. forms a molecule like water or weak acid

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Precipitation Reactions • What is a precipitate?

– Rain is called precipitation, Why? • When an ionic compound dissolves in

water, what actually happens?

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Precipitation Reactions Double Replacement

• K2CrO4(aq) + Ba(NO3)2 (aq) → Products – A yellow precipitate forms. What is it?

• Consider what is in solution K+ K+ CrO4

-2 Ba+2 NO3-1 NO3

-1 • Only two choices to precipitate BaCrO4↓ + K+ + NO3

-1 or K NO3 + CrO4

-2 + Ba+2

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Double Replacement Reactions

• Why does one replace the other? • Need to know the solubility of compounds

to predict these. • Yes, you must memorize them! K2CrO4(aq) + Ba(NO3)2 (aq) → BaCrO4↓ + K+ + NO3

-1 2K++ CrO4

-2 +Ba+2 + 2NO3-1 → BaCrO4↓ + 2K+ + 2NO3

-1

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Combustion of a Hydrocarbon

• Produces carbon dioxide and water

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•The Structure of Complex Ions • Ions of transition metals lose electrons to form small, highly charged cations.

• These positive ions attract negatively charged anions and/or the negative end of polar molecules, called ligands , to form coordinate covalent bonds, where both electrons from the shared pair come from the anion. • The resulting complex ions are charged: They have a metal ion (can be zero oxidation state) bonded to a number of ligands. Example, [Ag(NH3)2]

+.

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•The Structure of Complex Ions • The formation of complex ions can occur when insoluble compounds react with

ligands to dissolve in solution. • Examples: • Excess concentrated ammonia solution is added to a suspension of silver chloride.

•Al3+

(aq) + 3OH1-

(aq) → Al(OH)3(s) •Al(OH)3(s) + OH

1-(aq) → [Al(OH)4]

1-(aq)

• AgCl(s) + 2NH3(aq) → [Ag(NH3)2]1+

(aq) + Cl1-

(aq)

• Excess potassium hydroxide solution is added to a solution of aluminum nitrate.

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• Most metal ions in water exist as [M(H2O)6]n+

.

•The Structure of Complex Ions

•[Co(H2O)6]2+

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•The Structure of Complex Ions

• [Al(H2O)6 ]3+

(aq) + OH1-

(aq) → [Al(H2O)5(OH)]2+

(aq) + H2O(l) • [Al(H2O)5(OH)]

2+(aq) + OH

1-(aq) → [Al(H2O)4(OH)2]

1+(aq) + H2O(l)

• [Al(H2O)4(OH)2]1+

(aq) + OH1-

(aq) → [Al(H2O)3(OH)3](s) + H2O(l) • [Al(H2O)3(OH)3](s) + OH

1-(aq) → [Al(H2O)2(OH)4]

1-(aq) + H2O(l)

• Al3+

(aq) + 4OH1-

(aq) → [Al(OH)4]1-

(aq) •The reaction of aluminum and hydroxide ions actually occurs in several

steps:

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• The number of ligands attached to the metal is called the coordination number. • The size of the ligand affects the coordination number (e.g. [FeF6]

3- forms but only

[FeCl4]- is stable).

•The Structure of Complex Ions

•Fe •Cl

1-

•Cl1-

•Cl1-

•Cl1-

•1-

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• [Co(H2O)6]2+

(aq) + 4Cl1-

(aq) [CoCl4]2-

(aq) + 6H2O(l)

•The Structure of Complex Ions

•Co •Cl

1-

•Cl1-

•Cl1-

•Cl1-

•2-

•2+

• Concentrated hydrochloric acid is added to a solution of cobalt (II) chloride.

• pink color • blue color

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• As a general rule, the most stable complexes have a coordination number that is twice the charge of the metallic ion.

•The Structure of Complex Ions

•Complexes with a coordination number of 4 are either tetrahedral or square planar (commonly seen for d

8 metal ions).

•[Zn(NH3)4]2+

vs. [Pt(NH3)4]2+

•..

•..

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• Complexes with a coordination number of 6 form octahedral structures.

•The Structure of Complex Ions

•The relative strength of the bonds between the metallic ions and common ligands is: •Cl

- < F

- < H2O < NH3 < NO2

- (bonded at N) < CN

-

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•Chelates • Polydentate ligands (or chelating agents) bind to the metallic ion through more than

one donor atom per ligand.

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•Metals and Chelates in Living Systems • Many natural chelates are designed around the porphyrin molecule.

• After the two H atoms bound to N are lost, porphyrin is a tetradentate ligand.

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Chlorophyll a

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Myoglobin

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•Nomenclature • Rules: (in case you wanted to know) • For salts, name the cation before the anion. Example in [Co(NH3)5Cl]Cl2 we name [Co(NH3)5Cl]

2+ before the chloride, Cl

-. • Within a complex ion, the ligands are named (in alphabetical order) before the metal.

Example: [Co(NH3)5Cl]2+

is pentaamminechlorocobalt(III). Note the penta portion is an indication of the number of NH3 groups and is therefore not considered in the alphabetizing of the ligands. • Anionic ligands end in o and neutral ligands are simply the name of the molecule. Exceptions: H2O (aqua) and NH3 (ammine).

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