Unit 10 - Organic Chem
Transcript of Unit 10 - Organic Chem
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Organic ChemistryUnit 10
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HalidesPrimary Carbons
Secondary Carbons
Tertiary Carbons
IMPORTANCE??REACTIONS!!
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BenzeneC6H6
Aromatic functional group - C6H5 (IUPAC name - phenyl)
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Substitution Reactions of Alkanes - Halogenation
CH4(g) + Cl2(g) CH3Cl(g) + HCl(g)UV LIGHT
Reaction Mechanism - sequence of steps in a chemical reaction
Initiation - creating the free radical
Propagation - both use and produce free radicals
Termination - removing free radicals from the mixture
SHOW THE MECHANISM
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Alkanes vs Alkenesalkenes undergo addition where alkanes will not
different flame colors
burning of alkenes is dirtier - higher C:H ratio
Aromatic Compounds - Benzene Ring
Highly unsaturated - very smoky flame
Greenhouse gases, global warming, global dimming?
very high in residual C
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Alkenes - Electrophilic Additiondouble bonded carbons - one sigma bond and one pi bondAddition Reaction - attacks the weaker pi bond, therefore can be broken, leaving the sigma bond
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Alkenes - Electrophilic Addition
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Addition of Halogens
CH2CHCH3 + Cl2 CH2ClCHClCH3
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Hydrogenation
CH2CHCH3 + H2 CH3CH2CH3
Ni catalyst @ 150°C
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Addition of hydrogen halides
CH2CHCH3 + HCl CH2ClCH2CH3
This is only one possible product and maybe not the most likely
Markovnikov and stability of carbocations
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Carbocation Stability
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Addition of watermechanism on the board
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Polymerization
alkenes readily undergo addition to create long chains
mechanism for chloroethene
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ChallengeDraw the repeating unit of polystyrene if the formula of the monomer is C6H5CHCH2
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Alcohols
-OH functional group - polar - increases volatility and solubility of alkanes with similar molecular mass
most common alcohol - C2H5OH (ethanol) - readily soluble in water
don’t forget your lone pairs
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Oxidation of alcohols (different than combustion)
when looking to oxidize an alcohol, use an oxidizing agent (acidified potassium dichromate, colored)
Primary Alcohol Oxidation - two step
to an aldehyde first, then to a carboxylic acid
+ [O], heat + [O], heat
reflux
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REFLUX VS DISTILLATION
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Secondary Alcoholsoxidized to ketones by a similar process
+ [O], heat
reflux
CH3CH(OH)CH3
propan-2-ol(CH3)2CO
propanone
H+/Cr(VI) Cr(III)
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Tertiary Alcoholsnot readily oxidized under comparable conditions
would involve breaking the carbon skeleton
LOTS OF ENERGY!!!
+ [O], heat
refluxNO RXN!!
H+/Cr(VI) – NO COLOR CHANGE
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EsterificationCarboxylic acids and alcohols condense to form esters
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HalogenoalkanesSaturated, polar molecules
the carbon in this molecule is considered “electron poor”
nucleophile - reactants that are electron rich and hence attracted to regions of electron deficiency
leads to a reaction where the substitution of the halogen occurs
called Nucleophilic Substitution
shorthand - Sn
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Primary Halogenoalkanes - SN2 Mechanism
Overall reaction occurs with NaOH:
CH3Cl + OH- CH3OH + Cl-
Since hydrogen atoms are small, there are no “blockers” for the carbon to defend itself
Use polar aprotic solvents (acetonitrile, acetone)
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Tertiary Halogenoalkane: SN1 MechanismThe presence of 3 alkyl groups...what is happening?
This is called steric hindrance - bulky carbon atoms make it difficult for an incoming group to attack the carbon atom
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Secondary Halogenoalkanes?
What type of substitution do you think they undergo?
SN1 SN2
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Nucleophilic Substitution ReactionsOrganic Reactions are very sloooooooooooowww
Rate of reaction is important and studied heavily
Experiments show that:
SN1 is faster than SN2 reaction...why??
Which is the fastest rate of reaction...?
(primary/secondary/tertiary?)
TERTIARY > SECONDARY > PRIMARY
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Nucleophilic Substitution Reactions
Effect of Halogen on Nuc. Sub. Rxns
Two Opposing Factors to consider
1. Polarity of the C-Halogen bond
2. Strength of the C-Halogen bond
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Nucleophilic Substitution Reactions
Polarity - electronegativity decreases down a group (from F to Cl to Br to I)
Carbon is less and less electron deficient - less vulnerable to nucleophilic attack
Strength - as bond strength decreases down the group, the breakage of this bond is easier (iodoalkane is the most reactive, fluorine is the least)
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Nucleophilic Substitution Reactions
Based on the reaction data:
Strength is more important
Relative rate of reaction - -
iodoalkanes > bromoalkanes > chloroalkanes > fluoroalkanes
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Nucleophilic Substitution Reactions
These reactions are vital to many organic reactions
Allow for different synthetic reagents to be used
Conversions from halides to:
Alcohol
Amine
Nitrile
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Conversion into Alcohol
Bromoethane and NaOH --> ethanol and NaBr
Class of alcohol produced will match class of halide used in reaction
This will work with water, but is better with a base...
WHY?!?!
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Electrophilic Addition: alkenes
sp2 hybridized carbons (120˚ bond angles) results in an open structure - easy for groups to attack.
The pi (π) has electron density above and below. Weaker bond (less closely associated with nucleus).
The pi (π) bonds are attractive to electrophiles (species either electron deficient or that become electron deficient in the presence of a pi bond).
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Electrophilic Addition: alkenes
Ethene + bromine
Ethene + hydrogen bromide
Propene + hydrogen bromide (unsymmetric addition)
Markovnikov's rule
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Electrophilic Substitution: benzene
Benzene attractive to electrophiles.
High activation energy so slow reaction
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EAS: Nitration of benzene
substitution of –H by –NO2
Nitrating mixture: conc. HNO3 and conc. H2SO4
MECHANISM TO FOLLOW...
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Reduction ReactionsOxidation Review
Primary alcohol -> aldehyde -> carboxylic acid
Secondary alcohol -> ketone
Reduction - reverse the process
Sodium borohydride (NaBH4 in aqueous or alcoholic solution)
Lithium aluminum hydride (LiAlH4 in anhydrous conditions, diethyl ether followed by aqueous acid)
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Reduction ReactionsReduction of carboxylic acids
NaBH4 is the safer reagent, but it's not strong enough to reduce acids so we use LiAlH4 instead.
Reduction of nitrobenzene
2 stage process
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20.2 Synthetic RoutesSummary of reactions to date (p. 511... need to know it!)
Example: nitration of benzene -> phenylamine
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Retrosynthesis Target molecules (E.J. Corey, MIT, 1990 Nobel Prize winner)
Work backwards to starting materials
EXAMPLE: You are required to make butanone starting from any alkene of your choice. Show the steps involved in retrosynthesis to determine the identity of the alkene.
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StereoisomerismBuild 2-butene....GO!
Are all of our structures the same?
2 types of configurational stereoisomerism
Geometric: cis and trans isomers
Optical isomers: chirality
Geometric Isomers: occur with some constraint
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Isomerism in Organic Chemistry
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Now, you try it!
Draw and name the geometric isomers of butenedioic acid.
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Cyclic moleculesRing of carbon atoms which prevent rotation
Textbook gives several examples (p. 517)
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Physical PropertiesDepend on:
Polarity
Shape or symmetry
Name these:
What intermolecular forces will these undergo?
Which will have a higher boiling point?
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Physical Properties continued...
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Physical Properties continued...
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What happens when cis, trans doesn't work?
When the doubly bonded carbons are also bonded to more than one other group....
E/Z designation - based on Cahn-Ingold-Prelog rules of priority
Higher atomic number = greater priority
EXAMPLE: 1-BROMO-2-METHYLBUT-1-ENE
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Optical IsomersA carbon atom attached to four different atoms or groups is known as asymmetric or chiral
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Optical IsomersCan be arranged in two different 3-D configurations that are mirror images of each other
Known as optical isomerism
The term refers to the way the isomers react with plane polarized light
They are chiral molecules with NO plane of symmetry
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Plane of symmetryTry it with your hands...
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Enantiomers
The two non-superimposable forms of optical isomers
A mixture containing equal amounts of the two is known as a RACEMIC mixture
A racemic mixture is optically inactive...
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How do I know it's an optical isomer?
Find the C atom with four different groups bonded to it. It is useful to mark the CHIRAL carbon with an asterisk.
Try it!! Draw butan-2-ol. Find the chiral carbon. Mark it with an asterisk.
Draw 2-chlorobutane. Find the chiral carbon.
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Properties of Optical Isomers
Have identical physical and chemical properties
Except:
Optical activity
Reactivity with other chiral molecules
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Properties of Optical Isomers
• Think optical purity isn’t important?? • One enantiomer relieves morning sickness. The other causes
major birth defects.