organic(compounds(that( conductelectricity(...•...
TRANSCRIPT
![Page 1: Organic(Compounds(That( ConductElectricity(...• The(single(bond(between(the(conjugated(double(bonds(is(shorter(and(stronger(than(normal(• Thebonding(π@orbitals(are(made(from(4(p(orbitals(thatprovide(greater](https://reader037.vdocuments.net/reader037/viewer/2022090811/611cc6602099e364dd74cb5b/html5/thumbnails/1.jpg)
Organic Compounds That Conduct Electricity
Conjugated Systems
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• Compounds can have more than one double or triple bond
• If they are separated by only one single bond they are conjugated and their orbitals interact
• The conjugated diene 1,3-‐butadiene has properAes that are very different from those of the nonconjugated diene, 1,4-‐pentadiene.
Conjugated and Nonconjugated Dienes
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The Smaller the Heat of HydrogenaAon, the More Stable the Compound
Conjugated dienes are more stable than nonconjugated based on heats of hydrogenaAon
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Conjugated Dienes Have Delocalized Electrons
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An sp2–sp2 Bond Is Stronger Than an sp2–sp3 Bond
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Carbon-‐Carbon Bond Length Depends on HybridizaAon
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Cumulated Double Bonds
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Allyl and Benzyl Allylic and Benzylic
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Resonance Contributors for an Allylic CaAon
Resonance Contributors for a Benzylic CaAon
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RelaAve StabiliAes of CarbocaAons
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• Typically by eliminaAon in allylic halide • Specific industrial processes for large scale producAon of commodiAes by catalyAc dehydrogenaAon and dehydraAon
Stability of Conjugated Dienes: Molecular Orbital Theory
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• The single bond between the conjugated double bonds is shorter and stronger than normal
• The bonding π-‐orbitals are made from 4 p orbitals that provide greater delocalizaAon and lower energy than in isolated C=C
• The 4 molecular orbitals include fewer total nodes than in the isolated case
• In addiAon, the single bond between the two double bonds is strengthened by overlap of p orbitals
• In summary, we say electrons in 1,3-‐butadiene are delocalized over the π bond system – DelocalizaAon leads to stabilizaAon
Molecular Orbital DescripAon of 1,3-‐Butadiene
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An MO Diagram for Ethene
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An MO Diagram for 1,3-‐Butadiene
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Symmetric and AnAsymmetric Molecular Orbitals
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MO Diagrams for 1,4-‐Pentadiene and 1,3-‐Butadiene
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• Review: addiAon of electrophile to C=C – Markovnikov regiochemistry via more stable carbocaAon
Electrophilic AddiAons to Conjugated Dienes
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Mechanism
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Double Bonds Can Have Different ReacAviAes
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ReacAons of Conjugated Dienes
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1,2-‐AddiAon and 1,4-‐AddiAon
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• AddiAon of H+ leads to delocalized secondary allylic carbocaAon
CarbocaAons from Conjugated Dienes
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• Nucleophile can add to either caAonic site • The transiAon states for the two possible products are not equal
in energy
Products of AddiAon to Delocalized CarbocaAon
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Mechanism for the ReacAon of a Conjugated Diene
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Which Carbon Gets the Proton?
Protonate the end that forms the more stable carbocaAon:
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• At compleAon, all reacAons are at equilibrium and the relaAve concentraAons are controlled by the differences in free energies of reactants and products (Thermodynamic Control)
• If a reacAon is irreversible or if a reacAon is far from equilibrium, then the relaAve concentraAons of products depends on how fast each forms, which is controlled by the relaAve free energies of the transiAon states leading to each (Kine5c Control)
KineAc vs. Thermodynamic Control of ReacAons
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• AddiAon to a conjugated diene at or below room temperature normally leads to a mixture of products in which the 1,2 adduct predominates over the 1,4 adduct
• At higher temperature, the product raAo changes and the 1,4 adduct predominates
KineAc and Thermodynamic Control Example
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If the ReacAon is Irreversible, the KineAc Product Predominates
If the ReacAon is Reversible, the Thermodynamic Product Predominates
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Why?
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KineAc Control
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Thermodynamic Control
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DCl was used instead of HCl, so the 1,2-‐ and 1,4-‐products would be different.
The 1,2-‐Product is Always The KineAc Product
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The Proximity Effect
The proximity effect causes the 1,2-‐product to be formed faster.
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KineAc and Thermodynamic Products
Although the 1,2-‐product is always the kineAc product, do not assume that the 1,4-‐product is always the thermodynamic product.
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KineAc and Thermodynamic Products
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• Conjugate dienes can combine with alkenes to form six-‐membered cyclic compounds
• The formaAon of the ring involves no intermediate (concerted formaAon of two bonds)
• Discovered by O_o Paul Hermann Diels and Kurt Alder in Germany in the 1930’s
The Diels-‐Alder CycloaddiAon ReacAon
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The Mechanism
a pericyclic reacAon takes place by a cyclic shic of electrons
a [4+2] cycloaddiAon reacAon
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• Woodward and Hoffman showed this reacAon to be an example of the general class of pericyclic reac3ons
• Involves orbital overlap, change of hybridizaAon and electron delocalizaAon in transiAon state
• The reacAon is called a cycloaddi3on
View of the Diels-‐Alder ReacAon
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Faster if There is an Electron Withdrawing Group on the Dienophile
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• The alkene component is called a dienophile – C=C is conjugated to an electron withdrawing group, such as C=O or C≡N – Alkynes can also be dienophiles
CharacterisAcs of the Diels-‐Alder ReacAon
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The Electron Withdrawing Group Makes the Electrophile a Be_er Electrophile
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Another Diels–Alder ReacAon
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Alkynes Can Also Be Dienophiles
The cyclic product has two double bonds.
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Both Reactants are Not Symmetric
Two products are possible.
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The Reactants Can Be Aligned in Two Ways
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Which Alignment Gives The Major Product?
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• The relaAve posiAons of the two double bonds in the diene are “cis” or “trans” to each other about the single bond (being in a plane maximizes overlap)
• These conformaAons are called s-‐cis and s-‐trans (“s” stands for “single bond”)
• Dienes react in the s-‐cis conforma3on in the Diels-‐Alder reacAon
ConformaAons of Dienes in the Diels-‐Alder ReacAon
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s-‐Cis and s-‐Trans ConformaAons
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The Diene Must Be in an s-‐Cis ConformaAon
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Locked in an s-‐Cis ConformaAon
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Cis Forms Cis Trans Forms Trans
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• The reacAon is stereospecific, maintaining relaAve relaAonships from reactant to product – There is a one-‐to-‐one relaAonship between stereoisomeric reactants and products
Stereospecificity of the Diels-‐Alder ReacAon
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• Reactants align to produce endo (rather than exo) product – endo and exo indicate relaAve stereochemistry in bicyclic structures
– SubsAtuent on one bridge is exo if it is an3 (trans) to the larger of the other two bridges and endo if it is syn (cis) to the larger of the other two bridges
Regiochemistry of the Diels-‐Alder ReacAon
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Endo and Exo
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Bridged Bicyclic Rings and Fused Bicyclic Rings
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If the Diels–Alder ReacAon Creates an Asymmetric Center
A racemic mixture
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How to Determine the Reactants of a Diels–Alder ReacAon
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• Conjugated dienes can be polymerized • The iniAator for the reacAon can be a radical, or an acid • PolymerizaAon: 1,4 addiAon of growing chain to conjugated
diene monomer
Diene Polymers: Natural and SyntheAc Rubbers
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• A material from latex, in plant sap • In rubber repeaAng unit has 5 carbons and Z stereochemistry of all
C=C – Gu_a-‐Percha is natural material with E in all C=C
• Looks as if it is the head-‐to-‐tail polymer of isoprene (2-‐methyl-‐1,3-‐butadiene)
Natural Rubber
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• Chemical polymerizaAon of isoprene does not produce rubber (stereochemistry is not controlled)
• SyntheAc alternaAves include neoprene, polymer of 2-‐chloro-‐1,3-‐butadiene
• This resists weathering be_er than rubber
SyntheAc Rubber
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• Natural and syntheAc rubbers are too soc to be used in products
• Charles Goodyear discovered heaAng with small amount of sulfur produces strong material
• Sulfur forms bridges between hydrocarbon chains (cross-‐links)
VulcanizaAon