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C4H8O 1,2-EPOXYBUTANE

Epoxybutane and tetrahydrofuran both have the molecular formula C4H8O—that is, they are constitutional isomers—and so it is appropriate to compare their heats of combustion directly. Angle strain from the three-membered ring of 1,2-epoxybutane causes it to have more internal energy than tetrahydrofuran, and its combustion is more exothermic. [Pg.1650]

C4H8O 106-88-7 1,2-Epoxybutane see Ethyloxirane ... [Pg.47]

C4H8O 106-88-7 Ethyloxirane optical isomer> syn. 1,2-Butylene oxide 1,2-Epoxybutane 1,2-Butene oxide... [Pg.36]

See other pages where C4H8O 1,2-EPOXYBUTANE is mentioned: [Pg.1052]    [Pg.1088]    [Pg.1379]    [Pg.1549]    [Pg.2314]    [Pg.1065]    [Pg.1102]    [Pg.1429]    [Pg.1674]    [Pg.2483]    [Pg.1941]    [Pg.1089]    [Pg.1089]    [Pg.2029]    [Pg.1941]    [Pg.1941]    [Pg.350]    [Pg.97]    [Pg.342]    [Pg.1052]    [Pg.1088]    [Pg.1379]    [Pg.1549]    [Pg.2314]    [Pg.328]    [Pg.329]    [Pg.720]    [Pg.1065]    [Pg.1102]    [Pg.1429]    [Pg.1674]    [Pg.2427]    [Pg.2483]    [Pg.686]    [Pg.298]    [Pg.719]    [Pg.342]   
See also in sourсe #XX -- [ Pg.268 ]



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1.2- Epoxybutane

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