Two types of functional groups
2. ) everything else where a hydrogen is replaced by specific atoms or groups
Alkanes (alkyl)
Two prefixes:
n-CnH2n+1, n stand s for normal
i-CnH2n+1, i stands for iso
Reduction of alkyl halides
Catalyzed hydrogenation of Alkenes & alkynes to produce alkanes
2. ) alkyne + 2H2 -Pt/Ni-> alkane
Corey-House synthesis
2. ) R2CuLi + R’X -> R’R + RCu + LiX
Major reactions of alkanes
Thermal dehydrigenation
CnH2n+2 -heat-> mixture of smaller chain alkanes
Combustion
RH + O2 -> CO2 + 2H2O
Halogenation
RH + X2 -heat/light-> RX + HX
Halogenation initiation step
Forms reactive intermediate; a free radical of the halogen atom; electrophilic
Halogenation propagation step
2. ) alkyl radical reacts with halogen molecule
Halogenation termination step
Produces fewer radicals than it uses
Polymerization
Alkenes easily undergo the producing polymers
Synthesis of Alkenes
Dehydeogenation of alkanes to produce Alkenes
Alkane-heat&Pt/Pd-> alkene + H2
Dehydeogenation of alcohols to produce alkanes
Alcohol -acid-> alkene + H2O
Dehydrohalogenation of alkyl halides to produce alkene
RX -heat&base-> alkene
Dehalogenation of vicinal dihalides to produce Alkenes
XCH2-CH2X -Zn/Mg-> H2C=CH2 + ZnX2 or MgX2
Reduction of alkynes to produce Alkenes
Alkyne -Pd/BaSO4,H2,Quinoline-> alkene
Markovinkov’s rule
State that addition if a proton to the double bind of an alkene yields a product in which the proton is bonded to the carbon that already bears a greater # of hydrogens
Addition of hydrogen halides across double bonds (markovinkov addition)
H2C=CH2 + HX -> CH3CH2X
Hydration of Alkenes to produce alcohols (markovnikov addition)
H2C=CH2 + H2O -H+(cat)-> CH3CH2OH
Addition of H2SO4 to Alkenes to produce alcohols (markovnikov addition)
H2C=CH2 + H2SO4 -> CH3CH2-OSO3H -> CH3CH2OH
Oxymercuration-demercuration of Alkenes to produce alcohols (markovnikov addition)
H2C=CH2 + Hg(OAc)2 -H2O-> OHCH2CH2-HgOAc -NaBH4-> OHCH2CH3