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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).

  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. Leaving group - Wikipedia

    en.wikipedia.org/wiki/Leaving_group

    Here, a strong Lewis acid is required to generate either a carbocation from an alkyl halide in the Friedel-Crafts alkylation reaction or an acylium ion from an acyl halide.

  5. 2-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/2-Bromopropane

    Short-chain alkyl halides are often carcinogenic. The bromine atom is at the secondary position, which allows the molecule to undergo dehydrohalogenation easily to give propene, which escapes as a gas and can rupture closed reaction vessels. When this reagent is used in base catalyzed reactions, potassium carbonate should be used in place of sodium or potassium hydroxide.

  6. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    A functional group is a group of atoms in a molecule with distinctive chemical properties, regardless of the other atoms in the molecule. The atoms in a functional group are linked to each other and to the rest of the molecule by covalent bonds. For repeating units of polymers, functional groups attach to their nonpolar core of carbon atoms and ...

  7. Chloro (pyridine)cobaloxime - Wikipedia

    en.wikipedia.org/wiki/Chloro(pyridine)cobaloxime

    Chloro (pyridine)cobaloxime (III) is first reduced to Chloro (pyridine)cobaloxime (I) by sodium borohydride in alkaline solution, then an alkyl halide is added into the reaction mixture, and the desired Co-C bond is formed via a S N 2 reaction. This method can be used to produce cobaloximes containing a primary or a secondary alkyl substituent.

  8. Schiff base - Wikipedia

    en.wikipedia.org/wiki/Schiff_base

    General structure of an azomethine compound. In organic chemistry, a Schiff base (named after Hugo Schiff) is a compound with the general structure R1R2C=NR3 (R3 = alkyl or aryl, but not hydrogen). [1][2] They can be considered a sub-class of imines, being either secondary ketimines or secondary aldimines depending on their structure.

  9. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    Alkylation is the addition of alkyl groups to molecules, often by alkylating agents such as alkyl halides. Alkylating antineoplastic agents are a class of compounds that are used to treat cancer. In such case, the term alkyl is used loosely. For example, nitrogen mustards are well-known alkylating agents, but they are not simple hydrocarbons. In chemistry, alkyl is a group, a substituent, that ...

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