2.13 sources of alkanes and cycloalkanes
DESCRIPTION
2.13 Sources of Alkanes and Cycloalkanes. Crude oil. Crude oil. Naphtha (bp 95-150 °C). Kerosene (bp: 150-230 °C). C 5 -C 12. C 12 -C 15. Light gasoline (bp: 25-95 °C). C 15 -C 25. Gas oil (bp: 230-340 °C). Refinery gas. C 1 -C 4. Residue. Petroleum Refining. Cracking - PowerPoint PPT PresentationTRANSCRIPT
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2.132.13
Sources of Alkanes and CycloalkanesSources of Alkanes and Cycloalkanes
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Crude oilCrude oil
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Crude oilCrude oil
Refinery gasRefinery gasRefinery gasRefinery gas
CC11-C-C44
Light gasolineLight gasoline(bp: 25-95 °C)(bp: 25-95 °C)
Light gasolineLight gasoline(bp: 25-95 °C)(bp: 25-95 °C)
CC55-C-C1212
NaphthaNaphtha(bp 95-150 °C)(bp 95-150 °C)
NaphthaNaphtha(bp 95-150 °C)(bp 95-150 °C)
KeroseneKerosene(bp: 150-230 °C)(bp: 150-230 °C)
KeroseneKerosene(bp: 150-230 °C)(bp: 150-230 °C)
CC1212-C-C1515
Gas oilGas oil(bp: 230-340 °C)(bp: 230-340 °C)
Gas oilGas oil(bp: 230-340 °C)(bp: 230-340 °C)
CC1515-C-C2525
ResidueResidueResidueResidue
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CrackingCrackingconverts high molecular weight hydrocarbons converts high molecular weight hydrocarbons to more useful, low molecular weight onesto more useful, low molecular weight ones
ReformingReformingincreases branching of hydrocarbon chainsincreases branching of hydrocarbon chainsbranched hydrocarbons have better burningbranched hydrocarbons have better burningcharacteristics for automobile enginescharacteristics for automobile engines
Petroleum RefiningPetroleum Refining
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2.142.14
Physical Properties of AlkanesPhysical Properties of Alkanes
and Cycloalkanesand Cycloalkanes
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Boiling Points of Alkanes Boiling Points of Alkanes
governed by strength of intermolecular governed by strength of intermolecular attractive forcesattractive forces
alkanes are nonpolar, so dipole-dipole and alkanes are nonpolar, so dipole-dipole and dipole-induced dipole forces are absentdipole-induced dipole forces are absent
only forces of intermolecular attraction are only forces of intermolecular attraction are induced dipole-induced dipole forcesinduced dipole-induced dipole forces
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Induced dipole-Induced dipole attractive forcesInduced dipole-Induced dipole attractive forces
++––++ ––
two nonpolar moleculestwo nonpolar molecules
center of positive charge and center of negative center of positive charge and center of negative charge coincide in eachcharge coincide in each
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++––++ ––
movement of electrons creates an movement of electrons creates an instantaneous dipole in one molecule (left)instantaneous dipole in one molecule (left)
Induced dipole-Induced dipole attractive forcesInduced dipole-Induced dipole attractive forces
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++––++ ––
temporary dipole in one molecule (left) induces temporary dipole in one molecule (left) induces a complementary dipole in other molecule a complementary dipole in other molecule (right)(right)
Induced dipole-Induced dipole attractive forcesInduced dipole-Induced dipole attractive forces
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++––++ ––
temporary dipole in one molecule (left) induces temporary dipole in one molecule (left) induces a complementary dipole in other molecule a complementary dipole in other molecule (right)(right)
Induced dipole-Induced dipole attractive forcesInduced dipole-Induced dipole attractive forces
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++––++ ––
the result is a small attractive force between the result is a small attractive force between the two moleculesthe two molecules
Induced dipole-Induced dipole attractive forcesInduced dipole-Induced dipole attractive forces
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++–– ++ ––
the result is a small attractive force between the result is a small attractive force between the two moleculesthe two molecules
Induced dipole-Induced dipole attractive forcesInduced dipole-Induced dipole attractive forces
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increase with increasing number of carbonsincrease with increasing number of carbons
more atoms, more electrons, more more atoms, more electrons, more opportunities for induced dipole-inducedopportunities for induced dipole-induceddipole forces dipole forces
decrease with chain branchingdecrease with chain branching
branched molecules are more compact withbranched molecules are more compact withsmaller surface area—fewer points of contactsmaller surface area—fewer points of contactwith other molecules with other molecules
Boiling PointsBoiling Points
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increase with increasing number of carbonsincrease with increasing number of carbons
more atoms, more electrons, more more atoms, more electrons, more opportunities for induced dipole-inducedopportunities for induced dipole-induceddipole forces dipole forces
HeptaneHeptanebp 98°Cbp 98°C
OctaneOctanebp 125°Cbp 125°C
NonaneNonanebp 150°Cbp 150°C
Boiling PointsBoiling Points
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decrease with chain branchingdecrease with chain branching
branched molecules are more compact withbranched molecules are more compact withsmaller surface area—fewer points of contactsmaller surface area—fewer points of contactwith other molecules with other molecules
Octane: bp 125°COctane: bp 125°C
2-Methylheptane: bp 118°C2-Methylheptane: bp 118°C
2,2,3,3-Tetramethylbutane: bp 107°C2,2,3,3-Tetramethylbutane: bp 107°C
Boiling PointsBoiling Points
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All alkanes burn in air to giveAll alkanes burn in air to givecarbon dioxide and water.carbon dioxide and water.
2.152.15
Chemical Properties.Chemical Properties.
Combustion of AlkanesCombustion of Alkanes
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increase with increasing number of carbonsincrease with increasing number of carbons
more moles of Omore moles of O22 consumed, more moles consumed, more molesof COof CO22 and H and H22O formedO formed
Heats of CombustionHeats of Combustion
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4817 kJ/mol4817 kJ/mol
5471 kJ/mol5471 kJ/mol
6125 kJ/mol6125 kJ/mol
654 kJ/mol654 kJ/mol
654 kJ/mol654 kJ/mol
HeptaneHeptane
OctaneOctane
NonaneNonane
Heats of CombustionHeats of Combustion
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increase with increasing number of carbonsincrease with increasing number of carbons
more moles of Omore moles of O22 consumed, more moles consumed, more molesof COof CO22 and H and H22O formedO formed
decrease with chain branchingdecrease with chain branching
branched molecules are more stablebranched molecules are more stable(have less potential energy) than their(have less potential energy) than theirunbranched isomersunbranched isomers
Heats of CombustionHeats of Combustion
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5471 kJ/mol5471 kJ/mol
5466 kJ/mol5466 kJ/mol
5458 kJ/mol5458 kJ/mol
5452 kJ/mol5452 kJ/mol
5 kJ/mol5 kJ/mol
8 kJ/mol8 kJ/mol
6 kJ/mol6 kJ/mol
Heats of CombustionHeats of Combustion
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Isomers can differ in respect to their stability.Isomers can differ in respect to their stability.
Equivalent statement:Equivalent statement:
Isomers differ in respect to their potential energy.Isomers differ in respect to their potential energy.
Differences in potential energy can be measured by Differences in potential energy can be measured by comparing heats of combustion.comparing heats of combustion.
Important PointImportant Point
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8CO8CO22 + 9H + 9H22OO
5452 kJ/mol5452 kJ/mol5458 kJ/mol5458 kJ/mol
5471 kJ/mol5471 kJ/mol
5466 kJ/mol5466 kJ/molOO22++ 2525
22
OO22++ 2525
22 OO22++ 2525
22 OO22++ 2525
22
Figure 2.5Figure 2.5Figure 2.5Figure 2.5
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Oxidation of carbon corresponds to an Oxidation of carbon corresponds to an increase in the number of bonds between increase in the number of bonds between carbon and oxygen and/or a decrease carbon and oxygen and/or a decrease in the number of carbon-hydrogen bonds. in the number of carbon-hydrogen bonds.
2.162.16
Oxidation-Reduction in Organic Oxidation-Reduction in Organic
ChemistryChemistry
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increasing oxidation increasing oxidation state of carbonstate of carbon
-4-4 -2-2 00 +2+2 +4+4
HH
HH
HH
CC HH
HH
HH
HH
CC OOHH
OO
CCHHHH
OO
CCOOHHHH
OO
CCOOHHHHOO
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increasing oxidation increasing oxidation state of carbonstate of carbon
-3-3 -2-2 -1-1
HCHC CHCH
CC CC
HH
HH HH
HH
CC CC HH
HHHH
HH HH
HH
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But most compounds contain several (or many)But most compounds contain several (or many)carbons, and these can be in different oxidationcarbons, and these can be in different oxidationstates.states.
Working from the molecular formula gives Working from the molecular formula gives the average oxidation state.the average oxidation state.
CHCH33CHCH22OHOH CC22HH66OO
Average oxidationAverage oxidationstate of C = -2state of C = -2-3-3 -1-1
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Fortunately, we rarely need to calculate the Fortunately, we rarely need to calculate the oxidation state of individual carbons in a molecule oxidation state of individual carbons in a molecule ..
We often have to decide whether a process We often have to decide whether a process is an oxidation or a reduction.is an oxidation or a reduction.
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Oxidation of carbon occurs when a bond between Oxidation of carbon occurs when a bond between carbon and an atom which is less electronegative carbon and an atom which is less electronegative than carbon is replaced by a bond to an atom that than carbon is replaced by a bond to an atom that is more electronegative than carbon. The reverse is more electronegative than carbon. The reverse
process is reduction.process is reduction.
XX YY
XX less electronegative than carbon less electronegative than carbon
YY more electronegative than carbon more electronegative than carbon
oxidationoxidation
reductionreductionCC CC
GeneralizationGeneralization
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CHCH33ClCl HClHClCHCH44 ClCl22++ ++
OxidationOxidation
++ 2Li2Li LiClLiClCHCH33ClCl CHCH33LiLi ++
ReductionReduction
ExamplesExamples