Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie...

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Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders

Transcript of Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie...

Page 1: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Equilibrium, Redox Reactions, Hydrocarbons,

and Functional Groups

Chapters 18, 20, 22,

and 23

Jennie L. Borders

Page 2: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Chapter 18 – Reaction Rates and Equilibrium

A rate is a measure of the speed of any change that occurs within an interval of time.

In chemistry, the rate of chemical change or the reaction rate is usually expressed as the amount of reactant changing per unit of time.

Page 3: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 18.1 – Rate of Reaction According to collision theory, particles

can react to form products when they collide with one another, provided that the colliding particles have enough kinetic energy.

The minimum energy that colliding particles must have in order to react is called the activation energy.

Page 4: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Activation Energy

Page 5: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Transition State An activated complex is an unstable

arrangement of atoms that forms momentarily at the peak of the activation-energy barrier.

The activated complex is sometimes called the transition state.

Page 6: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Factors Affecting Reaction Rates

The rate of a chemical reaction depends upon temperature, concentration, particle size, and use of a catalyst.

Page 7: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Temperature Usually, raising the temperature speeds

up reactions. Increasing the temperature increases

both the frequency of collisions and the number of particles that have enough energy to slip over the activation-energy barrier.

Page 8: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Concentration The number of particles in a given

volume affects the rate at which reactions occur.

More particles increase the concentration which increase the number of collisions leading to a higher reaction rate.

Page 9: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Particle Size The surface area of a reactant affects

the reaction rate. The smaller the particle, the more

surface area. An increase in surface area increases

the amount of the reactant exposed for reaction.

Page 10: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Catalysts A catalyst increases the rate of reaction

without being used up during the reaction.

Catalysts permit the reaction to proceed along a lower energy path.

Page 11: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Catalyst vs. No Catalyst

catalyst

Page 12: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Catalysts Since a catalyst is not consumed during

a reaction, it does not appear as a reactant or a product.

Instead, the catalyst is written above the yield arrow.

Page 13: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Enzymes

Enzymes in your digestive tract act as catalysts for breaking down proteins.

It takes your body a few hours to digest proteins.

Without the enzymes, it would take many years for you to digest your food.

Page 14: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 18.1 Assessment

1. How is the rate of a chemical reaction expressed?

2. What are four factors that affect the rate of a chemical reaction?

3. Does every collision between reaction particles lead to products? Explain.

4. Why does refrigerated food stay fresh longer than room temperature food?

Page 15: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 18.2 - Equilibrium A reversible reaction is one in which the

conversion of reactants to products and the conversion of products to reactants occur simultaneously.

Page 16: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Equilibrium When the rates of the forward and

reverse reactions are equal, the reaction has reached chemical equilibrium.

At chemical equilibrium, no net change occurs in the actual amounts of the components of the system.

Page 17: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Position The relative concentrations of the

reactants and products at equilibrium constitute the equilibrium position of a reaction.

The equilibrium position indicates whether the reactants or products are favored in a reversible reaction.

Page 18: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Le Chatelier’s Principle Le Chatelier’s Principle states that if a

stress is applied to a system in equilibrium, the system changes in a way that relieves the stress.

Stresses that upset the equilibrium include changes in the concentration of reactants or products, change in temperature, or changes in pressure.

Page 19: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Concentration Changing the concentration of any

reactant or product at equilibrium disturbs the equilibrium.

The system adjusts to minimize the effects of the change by shifting the equilibrium.

Page 20: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Temperature Increasing the temperature causes the

equilibrium position to shift to the direction that absorbs heat.

Think of heat as a reactant or product in the reaction.

Page 21: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Pressure A change in pressure only affects

gaseous equilibria that have an unequal number of moles of reactants and products.

Page 22: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Sample Problem What effect do each of the following changes

have on the equilibrium position for this following reaction?

PCl5(g) + heat PCl3(g) + Cl2(g)

a. Addition of Cl2b. Increase in pressurec. Removal of heatd. Removal of PCl3 as it is formed

equilibrium shifts to the left

equilibrium shifts to the right

equilibrium shifts to the left

equilibrium shifts to the left

Page 23: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Equilibrium Constant The equilibrium constant (Keq) is the

ratio of the product concentration to reactant concentration at equilibrium, with each concentration raised to a power equal to the number of moles of that substance in the balanced chemical equation.

Page 24: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Equilibrium ConstantGeneric Reaction:

aA + bB cC + dD

Equilibrium Constant:

Keq = [C]c x [D]d

[A]a x [B]b

Page 25: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Equilibrium Constant Keq > 1, products favored at equilibrium Keq < 1, reactants favored at equilibrium

Page 26: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Sample Problem A liter of a gas mixture at equilibrium

contains 0.0045mol or N2O4 and 0.030mol of NO2. Calculate Keq.

N2O4(g) 2NO2(g)

Keq = [NO2]2 Keq = (0.030M)2 = 0.20 [N2O4] (0.0045M)

Page 27: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Practice Problem At equilibrium, a 1L flask contains 0.15

mol H2, 0.25 mol N2, and 0.10 mol NH3. Calculate Keq for the reaction.

N2 + 3H2 2NH3

Keq = [NH3]2 Keq = (0.10M)2 = 11.85 [N2][H2]3 (0.25)(0.15)3

Page 28: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 18.2 Assessment1. How do the amounts of reactants and

products change after a reaction has reached chemical equilibrium?

2. What are three stresses that can upset the equilibrium of a chemical system?

3. What does the value of the equilibrium constant tell you about the amounts of reactants and products present at equilibrium?

Page 29: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 18.2 Assessment4. How can a balanced chemical equation be used to write an equilibrium-constant expression?5. Can a pressure change shift the equilibrium position in every reversible reaction? Explain.6. Using the following equilibrium constants, determine which reactions would favor the products.

a. 1 x 102 b. 0.003 c. 3.5

Page 30: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Chapter 20 – Oxidation-Reduction Reactions

Oxidation-reduction reactions are also known as redox reactions.

Oxidation is the loss of electrons or the gain of oxygen.

Reduction is the gain of electrons or the loss of oxygen.

Page 31: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 20.1 - Oxidation vs. Reduction The way to remember the difference in

oxidation and reduction is OIL RIG.

O = oxidation I = is L = loss of electrons

R = reduction I = isG = gain of electrons

Page 32: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Oxidation-Reduction Reactions

Mg(s) + S(s) Mg+2S-2(s)

Mg has a 0 charge and changes to Mg+2, so it loses electrons and is oxidized.

S has a 0 charge and changes to S-2, so it gains electrons and is reduced.

Page 33: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Oxidizing and Reducing Agents The substance that loses electrons is

called the reducing agent. The substance that accepts electrons is

called the oxidizing agent. In other words, the substance that is

reduced is the oxidizing agent, and the substance that is oxidized is the reducing agent.

Page 34: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.
Page 35: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Sample ProblemDetermine what is oxidized and what is reduced. Identify the oxidizing agent and the reducing agent.

2AgNO3(aq) + Cu(s) Cu(NO3)2(aq) + 2Ag(s)

2Ag+NO3-(aq) + Cu0

(s) Cu+2(NO3-)2(aq) + 2Ag0

(s)

Ag goes from +1 to 0, so it gains electrons. Cu goes from 0 to +2, so it loses electrons.

Ag is reduced and is the oxidizing agent.Cu is oxidized and is the reducing agent.

Page 36: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Practice ProblemDetermine which substance is oxidized and which is reduced. Identify the oxidizing agent and the reducing agent.

4Al(s) + 3O2(g) 2Al2O3(s)

4Al0(s) + 3O20

(g) 2Al2+3O3-2

(s)

Al goes from 0 to +3, so it loses electrons. O goes from 0 to -2, so it gains electrons.

Al is oxidized and is the reducing agent.O is reduced and is the oxidizing agent.

Page 37: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 20.1 Assessment1. Define oxidation and reduction in

terms of loss or gain of oxygen.2. Define oxidation and reduction in

terms of loss or gain of electrons.3. How do you identify the oxidizing

agent and the reducing agent in a redox reaction?

Page 38: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 20.1 Assessment4. Determine which substance is oxidized and which is reduced. Identify the oxidizing agent and reducing agent.

Mg(s) + Cu(NO3)2(aq) Mg(NO3)2(aq) + Cu(s)

Mg0(s) + Cu+2(NO3

-)2(aq) Mg+2(NO3-)2(aq) + Cu0

(s)

Mg goes from 0 to +2, so it loses electrons. Cu goes from +2 to 0, so it gains electrons.

Mg is oxidized and is the reducing agent.Cu is reduced and is the oxidizing agent.

Page 39: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 20.2 – Oxidation Numbers An oxidation number is a

positive or negative number assigned to an atom to indicate its degree of oxidation or reduction.

A bonded atom’s oxidation number is the charge that it would have if the electrons in the bonded were assigned to the atom of the more electronegative element.

Page 40: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Rules for Oxidation Numbers1. The oxidation number of a monatomic ion is

equal to its ionic charge.Ex: Br- = -1 Fe+3 = +3

2. The oxidation number for H is +1 except in metal hydrides where it is -1.

Ex: HCl, H = +1 NaH, H = -1

3. The oxidation number for oxygen is -2 except in peroxides where it is -1.Ex: MgO, O = -2 H2O2, O = -1

Page 41: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Rules for Oxidation Numbers4. The oxidation number of a nonbonded

element is 0.Ex: Ag = 0 N2 = 0

5. For a neutral compound, the sum of the oxidation numbers must equal 0.

Ex: NaCl = +1 and -1 equal 0. H2O = 2(+1) and -2 equal 0.

6. For a polyatomic ion, the sum of the oxidation numbers must equal the ionic charge of the ion.

Ex: CO3-2, O = -2, so C = +4

4 + (3 x -2) = -2

Page 42: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Oxidation Numbers

Page 43: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Sample ProblemWhat is the oxidation number of each element in Na2SO4?

Na2SO4 = Na2+SO4

-2 so Na is +1

SO4-2 = O is -2, so S has to be +6

Na=+1, O=-2, and S=+6

Page 44: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Practice Problems1. Assign the oxidation numbers for each

element in SO2.

2. Assign the oxidation number for each element in (NH4)2S.

SO2, O = -2, so S would be +4

O=-2 and S=+4

(NH4)2S = (NH4)2+S-2, so S = -2

NH4+, H = +1, so N would be -3

N=-3, H=+1, and S = -2

Page 45: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Oxidation Numbers In some redox reactions, it is necessary

to look at oxidation numbers instead of just using charges.

Page 46: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Sample ProblemIdentify which atoms are oxidized and which are reduced in the reaction.

2KNO3(s) 2KNO2(s) + O2(g)

+1 +5 -2 +1 +3 -2 0

2KNO3(s) 2KNO2(s) + O2(g)

Since N went from +5 to +3, it is reduced.Since O went from -2 to 0, it is oxidized.

Page 47: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Practice ProblemIdentify which atoms are oxidized and which are reduced in the reaction.2HNO3(aq) + 6HI(aq) 2NO(g) + 3I2(s) + 4H2O(l)

+1 +5 -2 +1 -1 +2 -2 0 +1 -2

2HNO3(aq) + 6HI(aq) 2NO(g) + 3I2(s) + 4H2O(l)

Since N goes form +5 to +2, it is reduced.Since I goes form -1 to 0, it is oxidized.

Page 48: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 20.2 Assessment1. What is the general rule for assigning

oxidation numbers?2. Identify which atoms are oxidized and

which are reduced.2Na(s) + Cl2(g) 2NaCl(s)

0 0 +1 -1

2Na(s) + Cl2(g) 2NaCl(s)

Since Na goes from 0 to +1, it is oxidized.Since Cl goes from 0 to -1, it is reduced.

Page 49: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Chapter 22 – Hydrocarbon Compounds

Compounds that contain carbon are classified as organic compounds.

The simplest organic compounds contain only carbon and hydrogen and are called hydrocarbons.

Page 50: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 22.1 - Hydrocarbons

Because carbon has four valence electrons, a carbon atom always forms four covalent bonds.

Page 51: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Alkanes An alkane is a hydrocarbon in which

there are only single covalent bonds. The carbon atoms in an alkane can be

arranged in a straight chain or in a chain that has branches.

Page 52: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Naming Alkanes The following chart shows the names for

straight-chain alkanes containing 1 to 10 carbons.

# Carbon Name MolecularFormula

1  Methane  CH4 

2  Ethane  C2H6 

3  Propane  C3H8 

4  Butane  C4H10 

5  Pentane  C5H12 

6  Hexane  C6H14 

7  Heptane  C7H16 

8  Octane  C8H18 

9  Nonane  C9H20 

10  Decane  C10H22 

Page 53: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Writing the Formulas for Hydrocarbons

Molecular Formula C6H14

Page 54: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Branched-Chain Alkanes An atom or group of atoms that can take

the place of a hydrogen atom on a parent hydrocarbon is called a substituent.

The longest continuous carbon chain of a branched-chain hydrocarbon is called the parent alkane.

Page 55: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Alkyl Group A hydrocarbon substituent is called an

alkyl group. Alkyl groups are named by removing the

–ane ending from the parent hydrocarbon and adding –yl.

Ex: methane = methyl ethane = ethyl

Page 56: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Naming Branched-Chain Alkanes

The IUPAC rules for naming branched-chain alkanes are based on the name of the longest continuous carbon chain.

Each alkyl substituent is named according to the length of the chain and numbered according to its position on the main chain.

Page 57: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

IUPAC Rules1. The longest chain is the parent chain.2. Number the carbons in the parent

chain in order so that the groups attached to the chain will have the smallest numbers.

3. Add numbers to the names of the substituent groups to identify their positions.

Page 58: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

IUPAC Rules4. Use prefixes to indicate the appearance of the

same group more than once in the structural formula.

5. List the names of the alkyl substituents in alphabetical order, but ignore any prefixes.

6. Use proper punctuation.Commas are used to separate numbers, and hyphens are used to separate numbers andwords.

Page 59: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Sample Problems

Name the following compound.

4-ethyl-2,3-dimethylheptane

1 2 3 4 5 6 77 6 5 4 3 2 1

Page 60: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Sample Problems Name the following compound.

6

5

43 2 1

2,3,4-trimethylhexane

Page 61: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Practice Problems1. Name the following compound.

4 3 2 5

6 1

7

4-ethyl-3,3,4-trimethylheptane

Page 62: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Practice Problems1. Name the following compound.

4 3

5 2

6 1

7

4,4-diethylheptane

Page 63: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Drawing a Structural Formula

1. Write the parent chain (the ending of the name).

2. Number the carbons.3. Attach the substituent groups.4. Add hydrogens as needed until all

carbons have 4 bonds.

Page 64: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Sample Problem1. Draw the structural formula for 2,2,4-trimethylpentane.

1st draw pentane (5 carbons).

C - C - C - C - C

CH3

ICH3

I

ICH3

2nd add a methyl (-CH3) group to the 2, 2, and 4.

3rd fill in H’s until each C has 4 bonds.

H3 H2 H H3

Page 65: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Practice Problem1. Draw the structural formula for 4-ethyl-2,3,4-trimethyloctane.

1st draw octane (8 carbons).

2nd add an ethyl (CH3CH2-) to 4 and a methyl (CH3-)to 2, 3, and 4.3rd add H’s until each C has 4 bonds.

C - C - C - C - C - C - C - C ICH3

ICH3

ICH3

CH2CH3

IH3 H H H2 H2 H2 H3

Page 66: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 22.1 Assessment1. Explain why carbon atoms form four

covalent bonds.2. Write the structural formula for the

following alkanes.a. propane b. pentane

3. Draw the structural formula for 2,2-dimethylbutane.

CH3

ICH3-C-CH2-CH3

I CH3

Page 67: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 22.2 – Unsaturated Hydrocarbons Organic molecules that contain the

maximum amount of hydrogen atoms per carbon atoms are called saturated compounds.

Compounds that contain double or triple bonds are called unsaturated compounds.

AlkaneR–CH2–CH2–

R

Alkene R–CH=CH–R

Alkyne R–C≡C–R

Page 68: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Alkenes Alkenes are hydrocarbons that contain

one or more carbon-carbon double covalent bonds.

When naming alkenes, find the longest chain that includes the double bond and change the ending of the alkane name to –ene. Ex: butane = butene

Page 69: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Naming Alkenes The carbons should be numbered so

that the double bonded carbons have the lowest number.

Any substituents should follow the rules that we have already covered.

Page 70: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Alkynes Hydrocarbons that contain one or more

carbon-carbon triple bonds are called alkynes.

Alkynes are named like alkenes, except that the alkane name ending changes to –yne. Ex: propane = propyne

Page 71: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Sample Problem Name the following compound.

1 2 3 4 5 6 77 6 5 4 3 2 1

3-methyl-2-heptene

Page 72: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Practice Problem Name the following compound.

CH3 ICH3-CH2-C C-CH-CH-CH2-CH3

I CH2CH3

1 2 3 4 5 6 7 8

5-ethyl-6-methyl-3-octyne

Page 73: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 22.2 Assessment Describe the bonding between atoms in

an alkene. What types of bonds are present in an

alkyne? What is the difference between

saturated and unsaturated hydrocarbons?

Page 74: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Chapter 23 – Functional Groups

The substituents of organic molecules often contain oxygen, nitrogen, sulfur, and/or phosphorus.

A functional group is a specific arrangement of atoms in an organic compound that is capable of characteristic chemical reactions.

Page 75: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 23.1 – Functional Groups

The symbol R represents any carbon chains or rings attached to the functional group.

Double bonds and triple bonds are also considered functional groups.

A halocarbon is a carbon containing compound with a halogen substituent.

Page 76: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Functional Groups

phenyl

Page 77: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Functional Groups

Page 78: Equilibrium, Redox Reactions, Hydrocarbons, and Functional Groups Chapters 18, 20, 22, and 23 Jennie L. Borders.

Section 23.1 Assessment1. What is a halocarbon?2. Identify the functional group in each

structure.a. CH3-OH

b. CH3-CH2-NH2

c. C - OH II O

d. CH3-CH2-CH2-Br

e. CH3-CH2-O-CH2-CH3