Aliphatic functional groups & organic chemistry.
Ryder Whittaker Hawkins | SCH3UE | Ms. Pall | Colonel By S.S
in order of increasing precedence:
Name
Alkane
Prefix
alkylalkane
Suffix
alkane
Hybridisation
sp3
IMFA
London
Alkene
alkenylalkane
alkene
sp2
London
Alkyne
alkynylalkane
alkyne
sp
London
Various additions
Cycloaddition
Oxidation
haloalkane
alkyl halide
sp3
Dipoledipole
Substitution
Elimination
Haloalkane
Structure
Primary
Secondary
Tertiary
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Reactions
Combustion
Addition
Cracking
Isomerisation
Addition
Polymerisation
Oxidation
Ether
sp3
Dipoledipole
Addition
Ether cleavage
Hybridisation
sp3
IMFA
H-bonds
Reactions
alkoxyalkane
Name
Amine
Structure
Primary
Prefix
aminoalkane
Suffix
alkanamine
Secondary
H-bonds
Tertiary
Alcohol
Primary
Dipoledipole
hydroxyalkane
alkanol
sp3
H-bonds
Deprotonation
Nucleophilic substitution
Dehydration
Oxidation
Esterification
oxoalkane
ketoalkane
alkanone
sp2
Dipoledipole
Nucleophilic addition
Electrophilic addition
Secondary
Tertiary
Ketone
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Name
Aldehyde
Structure
Nitrile
Amide
Primary
Prefix
aldoalkane
formylalkane
Suffix
alkanal
Hybridisation
sp2
IMFA
Dipoledipole
Reactions
Nucleophilic addition
Reduction
Oxidation
cyanoalkane
alkanenitrile
carbamoylalkane
alkanamide
sp carbon
sp nitrogen
sp2 carbon
sp3 nitrogen
sp2 oxygen
Dipoledipole
H-bonds
Dipoledipole
Hydrolysis, Reduction,
Nucleophilic addition
Dehydration
Reduction
Secondary
H-bonds
Dipoledipole
Tertiary
Ester
Dipoledipole
alkoxycarbonylalkane alkyl
alkanoate
sp2 carbon
sp2, sp3
oxygen
Dipoledipole
intellectual property of ryder whittaker hawkins sch3ue
Nucleophilic substitution
(Saponification)
Reduction
Carboxylic
acid
carboxyalkane
alkanoic acid
sp2 carbon
sp2, sp3
oxygen
Dipoledipole
H-bonds
intellectual property of ryder whittaker hawkins sch3ue
Reduction
Esterification