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v
t
e
Alcohols
Straight-chain
primary
alcohols
(1°)
Methanol
(
C
1
)
Ethanol
(
C
2
)
1-Propanol
(
C
3
)
n
-Butanol
(
C
4
)
1-Pentanol
(
C
5
)
1-Hexanol
(
C
6
)
1-Heptanol
(
C
7
)
1-Octanol
(
C
8
)
1-Nonanol
(
C
9
)
1-Decanol
(
C
10
)
Undecanol
(
C
11
)
Dodecanol
(
C
12
)
Tridecan-1-ol
(
C
13
)
1-Tetradecanol
(
C
14
)
1-Pentadecanol
(
C
15
)
Cetyl alcohol
(
C
16
)
Heptadecan-1-ol
(
C
17
)
Stearyl alcohol
(
C
18
)
Nonadecan-1-ol
(
C
19
)
Arachidyl alcohol
(
C
20
)
Heneicosan-1-ol
(
C
21
)
Docosanol
(
C
22
)
Tricosan-1-ol
(
C
23
)
1-Tetracosanol
(
C
24
)
Pentacosan-1-ol
(
C
25
)
1-Hexacosanol
(
C
26
)
1-Heptacosanol
(
C
27
)
1-Octacosanol
(
C
28
)
1-Nonacosanol
(
C
29
)
Triacontanol
(
C
30
)
Hentriacontanol
(
C
31
)
Dotriacontanol
(
C
32
)
Tritriacontanol
(
C
33
)
Tetratriacontanol
(
C
34
)
Pentatriacontanol
(
C
35
)
Hexatriacontanol
(
C
36
)
1-Heptatriacontanol
(
C
37
)
1-Octatriacontanol
(
C
38
)
Nonatriacontan-1-ol
(
C
39
)
Tetracontanol
(
C
40
)
Other primary
alcohols
Isobutanol
(
C
4
)
Isoamyl alcohol
(
C
5
)
2-Methyl-1-butanol
(
C
5
)
Phenethyl alcohol
(
C
8
)
Tryptophol
(
C
10
)
Secondary
alcohols (2°)
Isopropanol
(
C
3
)
Cyclopropanol
(
C
3
)
2-Butanol
(
C
4
)
2-Pentanol
(
C
5
)
3-Pentanol
(
C
5
)
Cyclopentanol
(
C
5
)
2-Hexanol
(
C
6
)
3-Hexanol
(
C
6
)
Pinacolyl alcohol
(
C
6
)
Cyclohexanol
(
C
6
)
2-Heptanol
(
C
7
)
3-Heptanol
(
C
7
)
2-Octanol
(
C
8
)
Tertiary
alcohols (3°)
tert
-Butyl alcohol
(
C
4
)
tert
-Amyl alcohol
(
C
5
)
2-Methyl-2-pentanol
(
C
6
)
2-Methylhexan-2-ol
(
C
7
)
2-Methylheptan-2-ol
(
C
8
)
3-Methyl-3-pentanol
(
C
6
)
3-Methyloctan-3-ol
(
C
9
)
Preparations
Substitution
of
haloalkane
Carbonyl reduction
Ether cleavage
Hydrolysis
of
epoxide
Hydration
of
alkene
Ziegler process
Reactions
Deprotonation
Protonation
Alcohol oxidation
Glycol cleavage
Nucleophilic substitution
Fischer–Speier esterification
Williamson ether synthesis
Elimination reaction
Nucleophilic substitution
of
carbonyl group
Friedel-Crafts alkylation
Nucleophilic conjugate addition
Transesterification
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