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The dehydrogenation of 2-butanol is catalysed by copper, zinc, or bronze: CH 3 CH(OH)CH 2 CH 3 → CH 3 C(O)CH 2 CH 3 + H 2. This is used to produce approximately 700 million kilograms yearly. Other syntheses that have been examined but not implemented include Wacker oxidation of 2-butene and oxidation of isobutylbenzene, which is analogous to ...
Structure and properties Index of refraction, n D: 1.3807 at 15.9 °C Abbe number: 32 Dielectric constant, ε r: 18.5 ε 0 at 20 °C Bond strength: 2.67 pa Bond length: r. Bond angle? Magnetic susceptibility? Surface tension: 23.9 dyn/cm at 25 °C Viscosity [1] 0.5429 mPa·s at 0 °C 0.4284 mPa·s at 20 °C 0.3490 mPa·s at 40 °C 0.2482 mPa·s ...
Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 O H, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuOH, and t-BuOH).
Like other butanols, butan-2-ol has low acute toxicity. The LD 50 is 4400 mg/kg (rat, oral). [6]Several explosions have been reported [7] [8] [9] during the conventional distillation of 2-butanol, apparently due to the buildup of peroxides with the boiling point higher than that of pure alcohol (and therefore concentrating in the still pot during distillation).
1-Butanol, also known as butan-1-ol or n-butanol, is a primary alcohol with the chemical formula C 4 H 9 OH and a linear structure. Isomers of 1-butanol are isobutanol, butan-2-ol and tert-butanol. The unmodified term butanol usually refers to the straight chain isomer.
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If it connects at one of the non-terminal (internal) carbon atoms, it is secondary butyl or sec-butyl: −CH(CH 3)−CH 2 −CH 3 (preferred IUPAC name: butan-2-yl) The second isomer of butane, isobutane, can also connect in two ways, giving rise to two additional groups: