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  2. 3,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/3,3-Dimethylpentane

    In 1929 Graham Edgar and George Calingaert made 3,3-dimethylpentane and measured its physical characteristics for the first time. The measurements were at 20 °C, not the standard conditions used in later times. [3] For 3,3-dimethylpentane they measured a density of 0.6934 at 20 °C with a rate of change Δd/ΔT of 0.000848.

  3. List of water-miscible solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_water-miscible...

    The following compounds are liquid at room temperature and are completely miscible with water; ... Name CAS number CH 3 CHO: acetaldehyde: 75-07-0 CH 3 CO 2 H: acetic ...

  4. Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/Dimethylpentane

    Dimethylpentane may refer to: 2,2-Dimethylpentane; 2,3-Dimethylpentane; 2,4-Dimethylpentane; 3,3-Dimethylpentane This page was last edited on 17 March ...

  5. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Density (g cm-3) Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 3.69 –5.96 –5.87 K b & K f [1] Lauric acid: 298.9 44 –3.9 Acetic acid: 1.04 117.9 3.14 16.6 –3.90 K b [1] K f [2] Acetone: 0.78 56.2 1.67 –94.8 K b [3] Benzene: 0.87 80.1 2.65 5.5 –5.12 K b & K f [2 ...

  6. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    Hydrides of the main group elements (groups 13–17) are given the base name ending with -ane, e.g. borane (B H 3), oxidane (H 2 O), phosphane (P H 3) (Although the name phosphine is also in common use, it is not recommended by IUPAC). The compound P Cl 3 would thus be named substitutively as trichlorophosphane (with chlorine "substituting ...

  7. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, CH 3 −CH(OH)−COOH (lactic acid) is named 2-hydroxypropanoic acid with no "1" stated. Some traditional names for common carboxylic acids (such as acetic acid) are in such widespread use that they are retained in IUPAC nomenclature, [7] though systematic names like ethanoic acid are

  8. IUPAC nomenclature of chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The main structure of chemical names according to IUPAC nomenclature. The International Union of Pure and Applied Chemistry (IUPAC) has published four sets of rules to standardize chemical nomenclature. There are two main areas: IUPAC nomenclature of inorganic chemistry (Red Book) IUPAC nomenclature of organic chemistry (Blue Book)

  9. 2,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylpentane

    3 replacing hydrogen atoms on carbon atoms 2 and 3. It is an alkane ("paraffin" in older nomenclature), a fully saturated hydrocarbon ; specifically, one of the isomers of heptane . Like typical alkanes, it is a colorless flammable compound; under common ambient conditions, it is a mobile liquid, less dense than water.