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  2. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    1-Bromobutane is the precursor to n-butyllithium: [4] 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.

  3. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    A comparison of S N 1 to S N 2 reactions is to the right. On the left is an S N 1 reaction coordinate diagram. Note the decrease in ΔG ‡ activation for the polar-solvent reaction conditions. This arises from the fact that polar solvents stabilize the formation of the carbocation intermediate to a greater extent than the non-polar-solvent ...

  4. 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) 2-Bromobutane ( sec -butyl bromide or methylethylbromomethane)

  5. Butane-1-thiol - Wikipedia

    en.wikipedia.org/wiki/Butane-1-thiol

    Butane-1-thiol, also known as butyl mercaptan, is a volatile, clear to yellowish liquid with a fetid (extremely foul-smelling) odor, commonly described as "skunk" odor. In fact, 1-butanethiol is structurally similar to several major constituents of a skunk's defensive spray but is not actually present in the spray. [ 4 ]

  6. Tetrabutylammonium bromide - Wikipedia

    en.wikipedia.org/wiki/Tetrabutylammonium_bromide

    Tetrabutylammonium bromide can be prepared by the alkylation of tributylamine with 1-bromobutane. [2] Tetrabutylammonium bromide is used to prepare other salts of the tetrabutylammonium cation by salt metathesis reactions. [6] It serves as a source of bromide ions for substitution reactions. It is a commonly used phase transfer catalyst.

  7. n-Butyllithium - Wikipedia

    en.wikipedia.org/wiki/N-Butyllithium

    The standard preparation for n-BuLi is reaction of 1-bromobutane or 1-chlorobutane with Li metal: [3] 2 Li + C 4 H 9 X → C 4 H 9 Li + LiX (X = Cl, Br) If the lithium used for this reaction contains 1–3% sodium, the reaction proceeds more quickly than if pure lithium is used.

  8. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    The left hand side is the proportion of conformer i in an equilibrating mixture of M conformers in thermodynamic equilibrium. On the right side, E k (k = 1, 2, ..., M) is the energy of conformer k, R is the molar ideal gas constant (approximately equal to 8.314 J/(mol·K) or 1.987 cal/(mol·K)), and T is the absolute temperature. The ...

  9. 2-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/2-Bromopropane

    1-Bromobutane; 2-Bromobutane; Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ...