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  2. Oxford Chemistry Primers - Wikipedia

    en.wikipedia.org/wiki/Oxford_Chemistry_primers

    Structure and Reactivity in Organic Chemistry: Howard Maskill: 14 October 1999 82: Foundations of Science Mathematics: Worked Problems: D. S. Sivia and S. G. Rawlings: 14 October 1999 83: NMR Spectroscopy in Inorganic Chemistry (2nd edition) Jonathan A. Iggo, Konstantin Luzyanin: 30 April 2020 84: Computers in Chemistry: Pete Biggs: 6 January ...

  3. Outline of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Outline_of_organic_chemistry

    The following outline is provided as an overview of and topical guide to organic chemistry: Organic chemistry is the scientific study of the structure, properties, composition, reactions, and preparation (by synthesis or by other means) of carbon-based compounds, hydrocarbons, and their derivatives.

  4. M-MTDATA - Wikipedia

    en.wikipedia.org/wiki/M-MTDATA

    m-MTDATA - whose full name is 4,4',4"-Tris(N-3-methylphenyl-N-phenyl-amino) triphenylamine - is an organic molecule belonging to the class of starburst molecules, [3] often used as a material for the production of organic electronic devices. It is particularly appreciated for its hole-transporting ability and is widely used in OLED and other ...

  5. Mass spectral interpretation - Wikipedia

    en.wikipedia.org/wiki/Mass_spectral_interpretation

    Examining organic compounds, the relative intensity of the molecular ion peak diminishes with branching and with increasing mass in a homologous series. In the spectrum for toluene for example, the molecular ion peak is located at 92 m/z corresponding to its molecular mass .

  6. Physical organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Physical_organic_chemistry

    Physical organic chemistry is the study of the relationship between structure and reactivity of organic molecules.More specifically, physical organic chemistry applies the experimental tools of physical chemistry to the study of the structure of organic molecules and provides a theoretical framework that interprets how structure influences both mechanisms and rates of organic reactions.

  7. Degree of unsaturation - Wikipedia

    en.wikipedia.org/wiki/Degree_of_unsaturation

    For hydrocarbons, the DBE (or IHD) tells us the number of rings and/or extra bonds in a non-saturated structure, which equals the number of hydrogen pairs that are required to make the structure saturated, simply because joining two elements to form a ring or adding one extra bond (e.g., a single bond changed to a double bond) in a structure reduces the need for two H's.

  8. Color of chemicals - Wikipedia

    en.wikipedia.org/wiki/Color_of_chemicals

    This spectral perspective was first noted in atomic spectroscopy. Below is a rough table of wavelengths, colors and complementary colors. This utilizes the scientific CMY and RGB color wheels rather than the traditional RYB color wheel.

  9. Spectral Database for Organic Compounds - Wikipedia

    en.wikipedia.org/wiki/Spectral_Database_for...

    The EI-MS spectra were measured in a JEOL JMS-01SG or a JEOL JMS-700 spectrometers, by the electron ionization method, with an electronic accelerating voltage of 75 eV and an ion accelerating voltage of 8 – 10 kV. The direct or reservoir inlet systems were used. The accuracy of the mass number is 0.5. This collection contains ca. 25,000 EI-MS ...