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Butanol, hydrogenation

Methyl 1 butanol Hydrogen 1 Bromo 2 methylbutane Water... [Pg.289]

Iodine at the N-alkylcarbazole 3-position has been reductively removed with lithium aluminium hydride - and hydrogen-Raney nickel, and bromine at the same position has been removed with lithium-tcrt-butanol. Hydrogen-nickel at 600 psi has also been used to hydrogenolyze carbazole carbon-bromine bonds, and hydrogen-palladium/charcoal at 200°C to remove a 1-chlorine. ... [Pg.158]

The same plant (Fig. 9-5) may be used to ketonize either isopropanol or sec-butanol. Hydrogen is passed up through the dry alcohol kept at such a temperature that the hydrogen leaving the saturator carries with it an equal volume of alcohol vapor. The hydrogen flow is adjusted to evaporate 128 lb per hr of the alcohols, whichever is used. [Pg.522]

Ans. The intermolecular attractive forces in 1-butanol are much higher since 1-butanol hydrogen-bonds with itself. Ethyl acetate cannot hydrogen-bond with itself since there is no O—H group. [Pg.311]

Just as the fossil fuel and petrochemicals industries are closely connected, the production of the same but bio-based chemicals will be closely related to the manufacturing of biofuels. The focus of commercialization by using biomass as a feedstock is mainly on ethanol, biodiesel, butanol, hydrogen, Fischer-Tropsch fuels, methanol, methane, and MTBEyETBE (methyl- or ethyl-tert-butylether). These products can be used either as biofuels or chemicals for further converting. In the context of this chapter, only routes for the ethylene and propylene... [Pg.303]

Hydrogenation of 2-butanone forms racemic 2-butanol. Hydrogen adds to either face of the double bond. Addition of H2 to one face gives the (R) product, while addition to the other fece gives the (5) product. [Pg.186]

Processes based on mierobial fermentation are currently regarded as alternatives having the most potential in eonverting hemicelluloses into biofuels and chemicals such as ethanol, butanol, hydrogen, and succinic acid due to the advantages of low cost and environmental friendliness. Recent studies on biofuels and chemicals from hemicellulosic fermentation are shown in Table 7.2. [Pg.180]


See other pages where Butanol, hydrogenation is mentioned: [Pg.153]    [Pg.153]    [Pg.101]    [Pg.101]    [Pg.101]    [Pg.71]    [Pg.994]    [Pg.160]    [Pg.1064]    [Pg.70]    [Pg.403]    [Pg.293]    [Pg.246]    [Pg.70]    [Pg.1652]    [Pg.13]    [Pg.13]    [Pg.855]    [Pg.67]    [Pg.197]   


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1- Butanol reaction with hydrogen halides

2 Butanol reaction with hydrogen bromide

2- Butanol diastereotopic hydrogens

2-Butanol reaction with hydrogen

3 Methyl 2 butanol reaction with hydrogen chloride

Butanol butyraldehyde hydrogenation

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