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  2. 3-Methylhexane - Wikipedia

    en.wikipedia.org/wiki/3-Methylhexane

    3-Methylhexane is a branched hydrocarbon with two enantiomers. [2] It is one of the isomers of heptane. The molecule is chiral, and is one of the two isomers of heptane to have this property, the other being its structural isomer 2,3-dimethylpentane. The enantiomers are (R)-3-methylhexane [3] and (S)-3-methylhexane. [4]

  3. Transhalogenation - Wikipedia

    en.wikipedia.org/wiki/Transhalogenation

    C 3 H 5-Cl + NaF → R-F + NaCl This kind of reaction is called Finkelstein reaction . [ 2 ] However, it is also possible, for example, to produce phosphorus fluoride compounds by transhalogenating chlorine, bromine or iodine bound to phosphorus with a metal fluoride.

  4. Hydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrohalogenation

    This is due to the abstraction of a hydrogen atom by the alkene from the hydrogen halide (HX) to form the most stable carbocation (relative stability: 3°>2°>1°>methyl), as well as generating a halogen anion. A simple example of a hydrochlorination is that of indene with hydrogen chloride gas (no solvent): [4]

  5. Haloform reaction - Wikipedia

    en.wikipedia.org/wiki/Haloform_reaction

    In chemistry, the haloform reaction (also referred to as the Lieben haloform reaction) is a chemical reaction in which a haloform (CHX 3, where X is a halogen) is produced by the exhaustive halogenation of an acetyl group (R−C(=O)CH 3, where R can be either a hydrogen atom, an alkyl or an aryl group), in the presence of a base.

  6. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    C=C + X 2 → X−CC−X (X represents the halogens bromine or chlorine, and in this case, a solvent could be CH 2 Cl 2 or CCl 4). The product is a vicinal dihalide. This type of reaction is a halogenation and an electrophilic addition.

  7. List of isomers of nonane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_nonane

    3-Ethyl-2-methylhexane; 4-Ethyl-2-methylhexane; 3-Ethyl-3-methylhexane; 3-Ethyl-4-methylhexane; Pentane. Isomers where pentane is the longest chain Tetramethyl

  8. Hofmann–Löffler reaction - Wikipedia

    en.wikipedia.org/wiki/Hofmann–Löffler_reaction

    The Suárez modification of the Hofmann–Löffler–Freytag reaction was the basis of the new synthetic method developed by H. Togo et al. [42] [43] The authors demonstrated that various N-alkylsaccharins (N-alkyl-1,2-benzisothiazoline-3-one-1,1,-dioxides) 77 are easily prepared in moderate to good yields by the reaction of N-alkyl(o-methyl ...

  9. 2,2,4-Trimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,2,4-Trimethylpentane

    2,2,4-Trimethylpentane, also known as isooctane or iso-octane, is an organic compound with the formula (CH 3) 3 CCH 2 CH(CH 3) 2. It is one of several isomers of octane (C 8 H 18 ). This particular isomer is the standard 100 point on the octane rating scale (the zero point is n -heptane ).