chapter 12 unsaturated hydrocarbons (alkenes). where found/uses found in: animal fat, vegetable oil,...
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Chapter 12Chapter 12
Unsaturated Hydrocarbons
(Alkenes)
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Where found/usesWhere found/uses
Found in: animal fat, vegetable oil, rubber, Unsaturated fats have less tendency to
increase Used to make drugs, plastics,
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Alkenes DefinedAlkenes Defined
Carbon and hydrogen compound containing
General formula
Double bond is more
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Bonding in AlkenesBonding in Alkenes
sp2 hybridization, 120O bond angle, 3 equivalent bonds
Two types of bonds– Sigma bond () - Strong– Pi bond () – Weak
Overlap of unused p orbital creates the double bond
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Constitutional IsomersConstitutional Isomers
More possible isomers for alkenes– 1. – 2. – Butane and 2-methylpropane–
How many isomers are there for C6H12?
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Naming AlkenesNaming Alkenes
1. Find longest continuous chain containing 2. Family name changed from –ane to –ene3. Longest chain numbered from the end 4. Substituent names are used as prefixes and
preceded by numbers to indicate location5. A compound with two double bonds is a diene
and the name ends –diene. The name includes numbers to show both locations of the double bonds.
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CycloalkenesCycloalkenes
Ring structure with a double bond. Numbering of ring stars at one of the
carbons of the double bond and proceeds
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Cis – Trans StereoisomerismCis – Trans Stereoisomerism
Double bonds This allows for There are 2 possible 2-butene compounds,
each with different geometric arrangements.–
Difference is in the configuration – both compounds have the same connectivity.
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Vision and StereoisomersVision and Stereoisomers
See box on page 339
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ProblemProblem
Which of the following exist as a pair of cis and trans isomers?–
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Addition in AlkenesAddition in Alkenes
Double bond is reactive enough to allow the addition of– Hydrogen– – – Water
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Addition ContinuedAddition Continued
Symmetric addition –
– Catalytic hydrogenation – – Halogenation
Test for alkenes –
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Addition to alkenesAddition to alkenes
Asymmetric addition – Addition of water in the presence of Markovnikov Rule
– The major product is the one formed when the hydrogen from the asymmetric reagent adds to the carbon of the double bond that has more hydrogen. HCl + propene
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PolymersPolymers
Chains of (often) Synthetic – Natural – proteins, carbos, nucleic acidsPolyethylenePolyvinylchloride
–
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Oxidation of alkenesOxidation of alkenes
By combustion to give By MnO4
- :
By Cr2O72-:
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AlkynesAlkynes
Unsaturated hydrocarbons with a General formula: Similar chemistry to alkenes Ending changed to sp hybridization, 180o bond angle Single sigma bond, two pi bonds Addition reactions follow Markovnikov’s rule
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AromaticsAromatics
Alkanes, -enes, and –ynes are called aliphatic hydrocarbons.
Aromatics have Called aromatic because many have Found in vanilla,
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Properties of AromaticsProperties of Aromatics
Benzene ring is Halogens, hydrogen halides, water and
sulfuric acid Combustion of aromatics is
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Isomers and NamingIsomers and Naming
Common monosubstituted names–
Disubstituted are named like alkenes.–
Trisubstituted: use numbers
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NamingNaming
If there is a large aliphatic chain attached to the ring, use the word phenyl to show the benzene– 2-methyl-3-phenylbutane
The group
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Reactions of AromaticsReactions of Aromatics
Halogenation:
Nitration:
Sulfonation: Alkylation:
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ReationsReations
Selective oxidation– Phenylbutane reacted in the presence of hot,
acidic MnO4- or Cr2O7
2- gives benzoic acid
All 5 types of reactions leave the benzene ring intact.
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Fused Ring AromaticsFused Ring Aromatics
“Straight” rings– Napthalene - – Anthracene –
Bent rings– Phenanthrene– Benzanthracene– Benzopyrene– All carcinogens, found in car exhaust, cigarette smoke,
and burnt (barbecued) meat.