Template:Alcohols

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v t e Alcohols
Straight-chain primary alcohols (1°)	Methanol (C₁) Ethanol (C₂) 1-Propanol (C₃) n-Butanol (C₄) 1-Pentanol (C₅) 1-Hexanol (C₆) 1-Heptanol (C₇) 1-Octanol (C₈) 1-Nonanol (C₉) 1-Decanol (C₁₀) Undecanol (C₁₁) Dodecanol (C₁₂) Tridecan-1-ol (C₁₃) 1-Tetradecanol (C₁₄) 1-Pentadecanol (C₁₅) Cetyl alcohol (C₁₆) Heptadecan-1-ol (C₁₇) Stearyl alcohol (C₁₈) Nonadecan-1-ol (C₁₉) Arachidyl alcohol (C₂₀) Heneicosan-1-ol (C₂₁) Docosanol (C₂₂) Tricosan-1-ol (C₂₃) 1-Tetracosanol (C₂₄) Pentacosan-1-ol (C₂₅) 1-Hexacosanol (C₂₆) 1-Heptacosanol (C₂₇) 1-Octacosanol (C₂₈) 1-Nonacosanol (C₂₉) Triacontanol (C₃₀) Hentriacontanol (C₃₁) Dotriacontanol (C₃₂) Tritriacontanol (C₃₃) Tetratriacontanol (C₃₄) Pentatriacontanol (C₃₅) Hexatriacontanol (C₃₆) 1-Heptatriacontanol (C₃₇) 1-Octatriacontanol (C₃₈) Nonatriacontan-1-ol (C₃₉) Tetracontanol (C₄₀)
Other primary alcohols	Isobutanol (C₄) Isoamyl alcohol (C₅) 2-Methyl-1-butanol (C₅) Phenethyl alcohol (C₈) Tryptophol (C₁₀)
Secondary alcohols (2°)	Isopropanol (C₃) Cyclopropanol (C₃) 2-Butanol (C₄) 2-Pentanol (C₅) 3-Pentanol (C₅) Cyclopentanol (C₅) 2-Hexanol (C₆) 3-Hexanol (C₆) Pinacolyl alcohol (C₆) Cyclohexanol (C₆) 2-Heptanol (C₇) 3-Heptanol (C₇) 2-Octanol (C₈)
Tertiary alcohols (3°)	tert-Butyl alcohol (C₄) tert-Amyl alcohol (C₅) 2-Methyl-2-pentanol (C₆) 2-Methylhexan-2-ol (C₇) 2-Methylheptan-2-ol (C₈) 3-Methyl-3-pentanol (C₆) 3-Methyloctan-3-ol (C₉)
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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