Chapter · PDF fileChapter 15 Dienes, Resonance, and Aromacity Organic Chemistry, 5th ed....
Transcript of Chapter · PDF fileChapter 15 Dienes, Resonance, and Aromacity Organic Chemistry, 5th ed....
Chapter15Dienes,Resonance,andAroma0city
Organic Chemistry, 5th ed. Marc Loudon
Eric J. Kantorowski California Polytechnic State University San Luis Obispo, CA
Chapter15Overview
• 15.1StructureandStabilityofDienes• 15.2Ultraviolet‐VisibleSpectroscopy• 15.3TheDiels‐AlderReacAon• 15.4Review• 15.5Free• 15.6RelaAonship• 15.7Free
2
Classifica3onofDienes
• Dienes
• Cumulenes
• Non‐conjugated(“ordinary”)dienes
315.1StructureandStabilityofDienes
HeatsofForma3on
415.1StructureandStabilityofDienes
OriginofConjugatedDieneStability
• σbondswithmores‐characterarestronger
• ThesebondingdifferencesareesAmatedtoaccountfor5‐6kJmol‐1ofthestabilizaAon
• TheremainingstabilizaAonisaTributedtotheπsystem
515.1StructureandStabilityofDienes
MOPictureof1,3‐Butadiene
615.1StructureandStabilityofDienes
Delocaliza3on
• Theπ1MOshowsthattheelectrondensityisspreadacrosstheen0remolecule
• Theelectronsaresaidtobedelocalized
715.1StructureandStabilityofDienes
StructureofConjugatedDienes
• Thesp2‐sp2bondshortensthelengthofC2‐C3• Compare:sp3‐sp3=1.54Åandsp2‐sp3=1.50Å
• Increasings‐characterdecreasesbondlength
815.1StructureandStabilityofDienes
Conforma3onsofDienes
915.1StructureandStabilityofDienes
Conforma3onsofDienes
• NewmanprojecAons:
1015.1StructureandStabilityofDienes
CumulatedDienes
• Thecentralcarbonissp‐hybridized• Thetwopibondsaremutuallyperpendicular
• TheC=CstretchingabsorpAonis1950cm‐1,notfarfromthatofalkynes
1115.1StructureandStabilityofDienes
CumulatedDienes
1215.1StructureandStabilityofDienes
CumulatedDienes
• Cumulateddienesmaybechiraleventhoughtheylackanasymmetriccarbon
1315.1StructureandStabilityofDienes
UV‐VisSpectroscopy
• DienesandordinaryalkenesdisplaysimilarIRandNMRspectra
• UV‐visiblelightcanprobetheextentofconjugaAoninconjugatedsystems
• Nearultraviolet(200–400nm)andvisiblelight(400–750nm)arethemostusefulregionsoftheEMspectrum
1415.2Ultraviolet‐VisibleSpectroscopy
TheUV‐VisSpectrum
• Anabsorp0onspectrumisproducedinUV‐visspectroscopy
1515.2Ultraviolet‐VisibleSpectroscopy
Absorbance
• Absorbance(oropAcaldensity,OD)measurestheincidentradiaAonabsorbedbyasample
• λmax:ThewavelengthatthemaximumofanabsorpAonpeak
1615.2Ultraviolet‐VisibleSpectroscopy
Absorbance
• Beer‐LambertLaw(orBeer’sLaw):
• εisthemolarex3nc3oncoefficientormolarabsorp3vity
• ExAncAoncoefficient’sof104–105M‐1cm‐1arecommonforconjugatedmolecules
1715.2Ultraviolet‐VisibleSpectroscopy
• UV‐visisbasedonexcitaAonofπelectrons
PhysicalBasisofUV‐VisSpectroscopy
1815.2Ultraviolet‐VisibleSpectroscopy
UV‐VisandConjuga3on
• UV‐visismostusefulforconjugatedsystems
• Chromophore:ThestructuralfeatureofamoleculeresponsibleforitsUV‐visabsorpAon
1915.2Ultraviolet‐VisibleSpectroscopy
UV‐VisSpectroscopyofConjugatedSystems
• λmaxisthemostimportantpartoftheUV‐visspectrum
• Thelongertheconjugatedπ‐electronsystem,thehigherthewavelengthofabsorp0on
• π‐electronpromoAonoccursfromthehighest‐occupiedMOtothelowest‐unoccupiedMO(HOMO→LUMO)
2015.2Ultraviolet‐VisibleSpectroscopy
UV‐VisSpectroscopyofConjugatedSystems
2115.2Ultraviolet‐VisibleSpectroscopy
• Longerπ‐system→higherλmax
UV‐VisSpectroscopyofConjugatedSystems
2215.2Ultraviolet‐VisibleSpectroscopy
UV‐VisSpectroscopyofConjugatedSystems
2315.2Ultraviolet‐VisibleSpectroscopy
Es3ma3ngλmax
• ConformaAonaleffects:
• SubsAtuenteffects:
2415.2Ultraviolet‐VisibleSpectroscopy
TheDiels‐AlderReac3on
• Conjugateddienescanreactwithalkenes
• DiscoveredbyOToDielsandKurtAlderin1928(sharedNobelPrizeinchemistry1950)
2515.3TheDiels‐AlderReac0on
TheDiels‐AlderReac3on
• Cycloaddi3onreac3on:AnaddiAonreacAonthatresultsinformaAonofaring
• TheD‐AreacAoncanalsobeclassifiedasa1,4‐addi3onreac3onoraconjugateaddi3on
2615.3TheDiels‐AlderReac0on
PericyclicReac3ons
• AconcertedreacAonthatinvolvesacyclicflowofelectrons
• TheD‐AreacAoncanalsobeclassifiedasapericyclicreac3on
2715.3TheDiels‐AlderReac0on
OtherDienophilesandDienes
• Alkynescanalsoserveasthedienophile
• Cyclicdienescanleadtobicycliccompounds
2815.3TheDiels‐AlderReac0on
EffectofDieneConforma3on
2915.3TheDiels‐AlderReac0on
Conforma3onandReac3vity
3015.3TheDiels‐AlderReac0on
Transi3onStateoftheDiels‐AlderReac3on
3115.3TheDiels‐AlderReac0on
StereochemistryoftheDiels‐AlderReac3on
• TheconcertedtransiAonstateresultsinsyn‐addiAonofthedienetothedienophile
3215.3TheDiels‐AlderReac0on
StereochemistryoftheDiels‐AlderReac3on
• Syn‐addiAonisalsorevealedwithsubsAtuentsattheterminalendsofthediene
3315.3TheDiels‐AlderReac0on
StereochemistryoftheDiels‐AlderReac3on
• AlsonotethedifferentreacAoncondiAons
3415.3TheDiels‐AlderReac0on
StereochemistryoftheDiels‐AlderReac3on
• ThepreviousreacAonsalsohaveaddiAonalstereochemistryattheringjuncAon
• Thisissueariseswhenboththeterminalcarbonsofthedieneandthecarbonsofthedienophilearestereocenters
3515.3TheDiels‐AlderReac0on
EndoandExoProducts
• Endoproduct:ThealkenesubsAtuentsarecistotheouterdienesubsAtuents(Ro)
• Exoproduct:ThealkenesubsAtuentsaretranstotheouterdienesubsAtuents(Ro)
• Theendoproductgenerallyformsfaster
3615.3TheDiels‐AlderReac0on
EndoandExoProducts
• Endovsexoproductsarealsoobservedwhencyclicdienesareused
3715.3TheDiels‐AlderReac0on
1,2‐and1,4‐Addi3ons
• ConjugateddienesreactwithH‐Xlikenormalalkenes,buttwotypesofaddiAoncanoccur
• 1,2‐addi3on:Occursatadjacentcarbons• 1,4‐addi3on:Occurstocarbonsthathavea1,4‐relaAonship
3815.4Addi0onofHydrogenHalidestoConjugatedDienes
1,2‐and1,4‐Addi3ons
3915.4Addi0onofHydrogenHalidestoConjugatedDienes
1,2‐and1,4‐Addi3ons
4015.4Addi0onofHydrogenHalidestoConjugatedDienes
AllylicCarboca3ons
4115.4Addi0onofHydrogenHalidestoConjugatedDienes
MODiagramoftheAllylCa3on
4215.4Addi0onofHydrogenHalidestoConjugatedDienes
Delocaliza3onintheAllylCarboca3on
• Theπ1MOshowsthatπ electronsarespreadacrossallthreecarbons
• LewisnotaAon:
• Theπ2MOshowsthatelectrondeficiencyissplitbetweenC1andC3
4315.4Addi0onofHydrogenHalidestoConjugatedDienes
Kine3candThermodynamicControl
• AtlowT,thelessstable1,2‐productdominates
• ThemajorproductcanbeidenAfiedunderequilibraAngcondiAons
4415.4Addi0onofHydrogenHalidestoConjugatedDienes
Kine3candThermodynamicControl
• Kine3ccontrol:WhenproductsdonotcomeintoequilibriumunderthereacAoncondiAons
• Thermodynamiccontrol:WhenproductsdocomeintoequilibriumunderthereacAoncondiAons
4515.4Addi0onofHydrogenHalidestoConjugatedDienes
Kine3candThermodynamicControl
4615.4Addi0onofHydrogenHalidestoConjugatedDienes
Kine3candThermodynamicControl
• Anionpairexplainswhythe1,2‐productisformedmorerapidly
4715.4Addi0onofHydrogenHalidestoConjugatedDienes
DienePolymers
• 1,3‐ButadieneisoneofthemostimportantrawmaterialsofthesyntheAcrubberindustry
• Itcanbepolymerized:
4815.5DienePolymers
DienePolymers
• Acopolymercanalsobeformedifstyreneisadded
4915.5DienePolymers
DienePolymers
• Naturalrubberisanotherdienepolymer
5015.5DienePolymers
• Vulcaniza0oncanbeusedtoincreasethestrengthandrigidityofthepolymer
Resonance
• ResonancestructuresdescribeamoleculewhenasingleLewisstructureisinadequate
• Moleculeswithresonancehybridsareresonance‐stabilized
• Resonancestructureshelpusunderstandmolecularstructure,stability,andreac0vity
5115.6Resonance
DrawingResonanceStructures
• Atomsarenotmovedinresonancestructures• CurvedarrownotaAonisuseful
5215.6Resonance
Rela3veImportanceofResonanceStructures
• IdenAcalstructuresareequallyimportant
• CompleAngoctets
5315.6Resonance
Rela3veImportanceofResonanceStructures
• PosiAvechargesandelectronegaAveatoms
5415.6Resonance
Rela3veImportanceofResonanceStructures
• StructurallimitaAons
5515.6Resonance
ResonanceandMolecularGeometry
• ThelemstructureimpliesthatNissp3andtetrahedral
• …buttherightstructureimpliessp2andtrigonalplanar
• ThehybridizaAonopAonthatmaximizesanatom’sabilitytointeractmosteffec0velywithitsneighborsisbest–inthiscase,Nissp2
5615.6Resonance
UseofResonanceStructures
• Allotherthingsbeingequal,themoleculewiththegreaternumberofresonancestructuresismorestable
• Thiswasencounteredinthe1,2‐vs1,4‐addiAonofH‐Xtoadiene:
5715.6Resonance
Aroma3cCompounds
• ManyfragrantcompoundsarederivaAvesofbenzene
5815.7Introduc0ontoAroma0cCompounds
Benzene,aPuzzling“Alkene”
• Kekuléproposedthecurrentstructureforbenzenein1865(derivedfromadream)
• TheKekuléstructureportraysbenzeneasacyclictriene
• However,benzene’sreacAvitydoesnotparallelthatofalkenes
5915.7Introduc0ontoAroma0cCompounds
Benzene,aPuzzling“Alkene”
• Cyclohexeneaddsbrominereadily
• …asdoes1,3,5,7‐cyclooctatetraene(COT)
6015.7Introduc0ontoAroma0cCompounds
StructureofBenzene
• Kekulé’s“triene”vsbenzeneandresonance
• Benzeneisonecompound
• IthasonetypeofC‐Cbondthatissomewherebetweenasingleanddoublebond
6115.7Introduc0ontoAroma0cCompounds
ComparisonofStructures
6215.7Introduc0ontoAroma0cCompounds
TheBenzeneπSystem
• Eachcarboninbenzeneistrigonalplanarandsp2hybridized
• Hence,alloftheporbitalsinbenzeneareparallelandreadilyoverlap
6315.7Introduc0ontoAroma0cCompounds
TheCyclooctatetraeneπSystem
• COTisnotplanar,buttub‐shaped
6415.7Introduc0ontoAroma0cCompounds
StabilityofBenzene
• ReacAvity(orlackofit)isacrudewaytomeasureenergycontent
• Amoreprecisewayisviastandardheatsofforma0on,ΔH°f
• Benzene:ΔH°fperCHgroupis13.8kJmol‐1
• COT:ΔH°fperCHgroupis37.3kJmol‐1
• Theempiricalresonanceenergyinbenzeneis141kJmol‐1[(37.3–13.8)x6CHgroups]
6515.7Introduc0ontoAroma0cCompounds
CriteriaforAroma3city
1.AromaAccompoundscontainoneormoreringswithacyclicarrangementofporbitals
2.EveryatominanaromaAcringhasaporbital
3.AromaAcringsareplanar(orverynearlyso)
4.Theseporbitalsmustcontain4n+2πelectrons(n=0,1,2,…)
• ThesecriteriaarecollecAvelycalledHückel’s4n+2ruleorthe4n+2rule
6615.7Introduc0ontoAroma0cCompounds
FrostCircle
6715.7Introduc0ontoAroma0cCompounds
Summaryofthe4n+2Rule
• Cyclicconjugatedmoleculesandionswith4n+2electronsfillthebondingMOs
• ThebondingMOsinthesecompoundshaveverylowenergy
• Asaresult,thesemoleculeshavealargeresonanceenergy
6815.7Introduc0ontoAroma0cCompounds
Aroma3cHeterocycles
6915.7Introduc0ontoAroma0cCompounds
Aroma3cIons
7015.7Introduc0ontoAroma0cCompounds
Aroma3cPolycyclicCompounds
• TheHückel4n+2ruleappliesstrictlytosingleringcompounds
• However,manyfusedbicyclicandpolycycliccompoundsarealsoaromaAc
7115.7Introduc0ontoAroma0cCompounds
Aroma3cOrganometallicCompounds
7215.7Introduc0ontoAroma0cCompounds
An3aroma3cCompounds
• An3aroma3ccompounds:Containplanar,con0nuousringsof4nelectrons
• AnAaromaAccompoundsareespeciallyunstable
• TheFrostcirclewouldshowtwohalf‐filleddegenerateorbitals(π2andπ3)
7315.7Introduc0ontoAroma0cCompounds
Non‐Aroma3cCompounds
• COTcontainsaconAnuouscycleof4nelectrons
• However,COTisnotplanartherebyavoidinganAaromaAccharacter
• ItisesAmatedthatplanarCOT(whichisanAaromaAc)is58kJmol‐1lessstablethanthetubconformaAon
7415.7Introduc0ontoAroma0cCompounds