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  2. 2-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/2-Bromobutane

    Both compounds share the molecular formula C 4 H 9 Br. 2-Bromobutane is also known as sec-butyl bromide or methylethylbromomethane. Because it contains bromine, a halogen, it is part of a larger class of compounds known as alkyl halides. It is a colorless liquid with a pleasant odor.

  3. 2-Chlorobutane - Wikipedia

    en.wikipedia.org/wiki/2-Chlorobutane

    2-Chlorobutane, along with other alkyl halides, is a useful intermediate in many different organic reactions. The halogen group is an effective leaving group, leading to its use in both elimination and substitution reactions. In addition, the compound is also a candidate for coupling reactions via a Grignard reagent.

  4. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    Haloalkane or alkyl halides are the compounds which have the general formula "RX" where R is an alkyl or substituted alkyl group and X is a halogen (F, Cl, Br, I). Haloalkanes have been known for centuries. Chloroethane was produced in the 15th century. The systematic synthesis of such compounds developed in the 19th century in step with the ...

  5. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert-butyl group attached to a bromide substituent. This organobromine compound is used as a standard reagent in synthetic organic chemistry. It is a colorless liquid.

  6. Secondary (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Secondary_(chemistry)

    Secondary is a term used in organic chemistry to classify various types of compounds (e. g. alcohols, alkyl halides, amines) or reactive intermediates (e. g. alkyl radicals, carbocations). An atom is considered secondary if it has two 'R' Groups attached to it. [1] An 'R' group is a carbon containing group such as a methyl (CH 3).

  7. Thiol - Wikipedia

    en.wikipedia.org/wiki/Thiol

    Thiol with a blue highlighted sulfhydryl group.. In organic chemistry, a thiol (/ ˈ θ aɪ ɒ l /; [1] from Ancient Greek θεῖον (theion) 'sulfur' [2]), or thiol derivative, is any organosulfur compound of the form R−SH, where R represents an alkyl or other organic substituent.

  8. Pseudohalogen - Wikipedia

    en.wikipedia.org/wiki/Pseudohalogen

    Examples of non-symmetrical pseudohalogen compounds (pseudohalogen halides Ps−X, where Ps is a pseudohalogen and X is a halogen, or interpseudohalogens Ps 1 −Ps 2, where Ps 1 and Ps 2 are two different pseudohalogens), analogous to the binary interhalogen compounds, are cyanogen halides like cyanogen chloride (Cl−CN), cyanogen bromide (Br ...

  9. Allyl bromide - Wikipedia

    en.wikipedia.org/wiki/Allyl_bromide

    Allyl bromide (3-bromopropene) is an organic halide. It is an alkylating agent used in synthesis of polymers, pharmaceuticals, perfumes [2] and other organic compounds. Allyl bromide is a colorless liquid, although commercial samples appear yellow or brown. It is an irritant and a potentially dangerous alkylating agent.

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