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  2. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    2 Li + C 4 H 9 X → C 4 H 9 Li + LiX where X = Cl, Br. The lithium for this reaction contains 1-3% sodium. When bromobutane is the precursor, the product is a homogeneous solution, consisting of a mixed cluster containing both LiBr and LiBu. 1-Fluorobutane can be obtained by reacting 1-bromobutane with potassium fluoride in ethylene glycol. [5]

  3. Bromoethane - Wikipedia

    en.wikipedia.org/wiki/Bromoethane

    H 2 C=CH 2 + HBr → H 3 C-CH 2 Br. Bromoethane is inexpensive and would rarely be prepared in the laboratory. A laboratory synthesis includes reacting ethanol with a mixture of hydrobromic and sulfuric acids. An alternate route involves refluxing ethanol with phosphorus and bromine; phosphorus tribromide is generated in situ. [4]

  4. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    The compound with the formula (C 5 H 5) 2 Fe 2 (CO) 4 exists as three isomers in solution. In one isomer the CO ligands are terminal. When a pair of CO are bridging, cis and trans isomers are possible depending on the location of the C 5 H 5 groups. [7] Another example in organometallic chemistry is the linkage isomerization of ...

  5. Bromobutane - Wikipedia

    en.wikipedia.org/wiki/Bromobutane

    Bromobutane (molecular formula: C 4 H 9 Br, molar mass: 137.02 g/mol) may refer to either of two chemical compounds: 1-Bromobutane (n-butyl bromide)

  6. Stoichiometry - Wikipedia

    en.wikipedia.org/wiki/Stoichiometry

    In the example above, reaction stoichiometry measures the relationship between the quantities of methane and oxygen that react to form carbon dioxide and water. Because of the well known relationship of moles to atomic weights , the ratios that are arrived at by stoichiometry can be used to determine quantities by weight in a reaction described ...

  7. Butanol - Wikipedia

    en.wikipedia.org/wiki/Butanol

    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).

  8. Bromophenol - Wikipedia

    en.wikipedia.org/wiki/Bromophenol

    Monobromrophenols have three isomers because there is only one bromine atom that can occupy one of three ring positions on the phenol molecule; 2-bromophenol, for example, is the isomer that has a bromine atom in the ortho position.

  9. Isobutyraldehyde - Wikipedia

    en.wikipedia.org/wiki/Isobutyraldehyde

    Isobutyraldehyde is the chemical compound with the formula (CH 3) 2 CHCHO. It is an aldehyde, isomeric with n-butyraldehyde (butanal). [1] Isobutyraldehyde is made, often as a side-product, by the hydroformylation of propene. Its odour is described as that of wet cereal or straw. It undergoes the Cannizzaro reaction even though it has alpha ...