Chiral centre in organic chemistry is most often an asymmetrically substituted carbon atom (C*).
The International Union of Pure and Applied Chemistry (IUPAC) is a non-governmental organization of member countries that encompasses more than 85% of the world’s chemical sciences and industries. It was formed in 1919 with the object of facilitating international agreement and uniform practice in both academic and industrial aspects of chemistry.
Meta position in organic chemistry is the one in which there are two same functional groups tied to a ring of benzene in position 1 and 3. The abbreviation m- is used, for example, m-Hydroquinone is 1,3-dihydroxybenzene.
Nuclear magnetic resonance (NMR) is a type of radio-frequency spectroscopy based on the magnetic field generated by the spinning of electrically charged atomic nuclei. This nuclear magnetic field is caused to interact with a very large (1 T - 5 T) magnetic field of the instrument magnet. NMR techniques have been applied to studies of electron densities and chemical bonding and have become a fundamental research tool for structure determinations in organic chemistry.
Ortho position in organic chemistry is the one in which there are two same functional groups, tied to a ring of benzene in the positions 1 and 2. The abbreviation o- is used, for example, o-Hydroquinone is 1,2-dihydroxybenzene.
Para position in organic chemistry is the one in which there are two same functional groups tied to a ring of benzene in the position 1 and 4. The abbreviation p- is used, for example, p-Hydroquinone is 1,4-dihydroxybenzene.
Acid halide is organic compound containing the group -COX where X is a halogen atom.
Acrylic acid (propenoic acid) is a colourless liquid, smelling like acetic acid. It can be formed by acrolein oxidation. It readily polymerizes and is used in the manufacture of acrylic resins, transparent plastic materials (organic glass).
Activated charcoal or activated carbon is charcoal that has been activated for adsorption by steaming or by heating in a vacuum. Charcoal is obtained by burning wood, nutshells, coconut husks or other materials. Charcoal becomes activated by heating it with steam to approximately 1000 °C in the absence of oxygen.
The chemical nature of amorphous carbon, combined with a high surface area makes it an ideal medium for the adsorption of organic chemicals. A single gram of such material can have 400 m2 to 1 200 m2 square meters of surface area. Activated charcoal is widely used to decolorize liquids, recover solvents, and remove toxins from water and air.
Generalic, Eni. "Organic chemistry." Croatian-English Chemistry Dictionary & Glossary. 29 June 2022. KTF-Split. {Date of access}. <https://glossary.periodni.com>.
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