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  2. Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Butyl_bromide

    Download as PDF; Printable version; In other projects Wikimedia Commons ... Butyl bromide (C 4 H 9 Br) may refer to: 1 -Bromobutane (n-Butyl bromide) 2 ...

  3. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    As a primary haloalkane, it is prone to S N 2 type reactions. It is commonly used as an alkylating agent. When combined with magnesium metal in dry ether, it gives the corresponding Grignard reagent. Such reagents are used to attach butyl groups to various substrates. 1-Bromobutane is the precursor to n-butyllithium: [4] 2 Li + C 4 H 9 X → C ...

  4. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    In organic chemistry, butyl is a four-carbon alkyl radical or substituent group with general chemical formula −C 4 H 9, derived from either of the two isomers (n-butane and isobutane) of butane. The isomer n -butane can connect in two ways, giving rise to two "-butyl" groups:

  5. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Silver bromide (AgBr). Nearly all elements in the periodic table form binary bromides. The exceptions are decidedly in the minority and stem in each case from one of three causes: extreme inertness and reluctance to participate in chemical reactions (the noble gases, with the exception of xenon in the very unstable XeBr 2; extreme nuclear instability hampering chemical investigation before ...

  6. Bromobutane - Wikipedia

    en.wikipedia.org/wiki/Bromobutane

    2-Bromobutane (sec-butyl bromide or methylethylbromomethane) Index of chemical compounds with the same name This set index article lists chemical compounds articles associated with the same name.

  7. Metal–halogen exchange - Wikipedia

    en.wikipedia.org/wiki/Metal–halogen_exchange

    An intramolecular S N 2 reaction by the anion forms the cyclic backbone of morphine. [14] Synthesis of morphine using lithium–halogen exchange. Lithium–halogen exchange is a crucial part of Parham cyclization. [15] In this reaction, an aryl halide (usually iodide or bromide) exchanges with organolithium to form a lithiated arene species.

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    www.aol.com/want-shape-2025-tell-us-023402315.html

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  9. Tetrabutylammonium chloride - Wikipedia

    en.wikipedia.org/wiki/Tetrabutylammonium_chloride

    Tetrabutylammonium chloride is the organic compound with the formula [(CH 3 CH 2 CH 2 CH 2) 4 N] + Cl −, often abbreviated as [Bu 4 N]Cl, where Bu stands for n-butyl. A white water-soluble solid, it is a quaternary ammonium salt of chloride. It is a precursor to other tetrabutylammonium salts.