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  2. 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 ...

  3. 2-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/2-Bromobutane

    2-Bromobutane is an isomer of 1-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.

  4. Allyl group - Wikipedia

    en.wikipedia.org/wiki/Allyl_group

    Allyl group. In organic chemistry, an allyl group is a substituent with the structural formula −CH2−HC=CH2. It consists of a methylene bridge (−CH2−) attached to a vinyl group (−CH=CH2). [1][2] The name is derived from the scientific name for garlic, Allium sativum. In 1844, Theodor Wertheim isolated an allyl derivative from garlic ...

  5. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    1-Bromobutane is the organobromine compound with the formula CH 3 (CH 2) 3 Br. It is a colorless liquid, although impure samples appear yellowish. It is insoluble in water, but soluble in organic solvents. It is primarily used as a source of the butyl group in organic synthesis. It is one of several isomers of butyl bromide.

  6. Markovnikov's rule - Wikipedia

    en.wikipedia.org/wiki/Markovnikov's_rule

    The chemical basis for Markovnikov's Rule is the formation of the most stable carbocation during the addition process. The addition of the hydrogen ion to one carbon atom in the alkene creates a positive charge on the other carbon, forming a carbocation intermediate. The more substituted the carbocation, the more stable it is, due to induction ...

  7. 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.

  8. Aryl halide - Wikipedia

    en.wikipedia.org/wiki/Aryl_halide

    Aryl halide. In organic chemistry, an aryl halide (also known as haloarene) is an aromatic compound in which one or more hydrogen atoms, directly bonded to an aromatic ring are replaced by a halide. Haloarenes are different from haloalkanes because they exhibit many differences in methods of preparation and properties.

  9. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    Alkyl group. In organic chemistry, an alkyl group is an alkane missing one hydrogen. [1] The term alkyl is intentionally unspecific to include many possible substitutions. An acyclic alkyl has the general formula of −CnH2n+1. A cycloalkyl group is derived from a cycloalkane by removal of a hydrogen atom from a ring and has the general formula ...

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