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  2. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    Alkyl groups form homologous series. The simplest series have the general formula −C n H 2n+1. Alkyls include methyl, (−CH 3), ethyl (−C 2 H 5), propyl (−C 3 H 7), butyl (−C 4 H 9), pentyl (−C 5 H 11), and so on. Alkyl groups that contain one ring have the formula −C n H 2n−1, e.g. cyclopropyl and cyclohexyl.

  3. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  4. List of isomers of tetradecane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_tetradecane

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  5. Gutmann–Beckett method - Wikipedia

    en.wikipedia.org/wiki/Gutmann–Beckett_method

    Gutmann, a chemist renowned for his work on non-aqueous solvents, described an acceptor-number scale for solvent Lewis acidity [4] with two reference points relating to the 31 P NMR chemical shift of Et 3 PO in the weakly Lewis acidic solvent hexane (δ = 41.0 ppm, AN 0) and in the strongly Lewis acidic solvent SbCl 5 (δ = 86.1 ppm, AN 100).

  6. Hagemann's ester - Wikipedia

    en.wikipedia.org/wiki/Hagemann's_ester

    2-Methoxy-1,3-butadiene and ethyl-2-butynoate undergo a Diels-Alder reaction to generate a precursor which is hydrolyzed to obtain Hagemann's ester. By varying the substituents on the butynoate starting material, this approach allows for different C2 alkylated Hagemann's ester derivatives to be synthesized.

  7. 3-Ethylpentane - Wikipedia

    en.wikipedia.org/wiki/3-ethylpentane

    3-Ethylpentane (C 7 H 16) is a branched saturated hydrocarbon. It is an alkane, and one of the many structural isomers of heptane, consisting of a five carbon chain with a two carbon branch at the middle carbon. An example of an alcohol derived from 3-ethylpentane is the tertiary alcohol 3-ethylpentan-3-ol. [3]

  8. Pentaethylenehexamine - Wikipedia

    en.wikipedia.org/wiki/Pentaethylenehexamine

    Pentaethylenehexamine is a hexadentate ligand, owing to the Lewis basicity of the six amine groups. [3] Pentaethylenehexamine is in the category of polyethyleneamines and is part of mixtures of these sold commercially. [2] Commercial supplies of pentaethylenehexamine contain, in addition to the linear form, branched and cyclic polyamines. [2]

  9. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    3-methyl-1-butanol or isoamyl alcohol or isopentyl alcohol primary 3-Methylbutan-1-ol: 131.2 2,2-dimethyl-1-propanol or neopentyl alcohol primary 2,2-Dimethylpropan-1-ol: 113.1 2-pentanol or sec-amyl alcohol or methyl (n) propyl carbinol secondary Pentan-2-ol: 118.8 3-methyl-2-butanol or sec-isoamyl alcohol or methyl isopropyl carbinol secondary