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  2. IUPAC numerical multiplier - Wikipedia

    en.wikipedia.org/wiki/IUPAC_numerical_multiplier

    di- 31 hentriaconta- 3 tri- 32 dotriaconta- 4 tetra- 33 tritriaconta- 5 penta- 34 tetratriaconta- 6 hexa- 40 tetraconta- 7 hepta- 50 pentaconta- 8 octa- 60 hexaconta- 9 nona- 70 heptaconta- 10 deca- 80 octaconta- 11 undeca- 90 nonaconta- 12 dodeca- 100 hecta- 13 trideca- 200 dicta- 14 tetradeca- 300 tricta- 15 pentadeca- 400 tetracta- 16 hexadeca-

  3. Numeral prefix - Wikipedia

    en.wikipedia.org/wiki/Numeral_prefix

    The IUPAC nomenclature of organic chemistry, for example, uses the numerical prefixes derived from Greek, except for the prefix for 9 (as mentioned) and the prefixes from 1 to 4 (meth-, eth-, prop-, and but-), which are not derived from words for numbers.

  4. IUPAC nomenclature of inorganic chemistry - Wikipedia

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

    The names "caffeine" and "3,7-dihydro-1,3,7-trimethyl-1H-purine-2,6-dione" both signify the same chemical compound.The systematic name encodes the structure and composition of the caffeine molecule in some detail, and provides an unambiguous reference to this compound, whereas the name "caffeine" simply names it.

  5. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    Thus, NCl 3 is termed nitrogen trichloride, BF 3 is termed boron trifluoride, and P 2 O 5 is termed diphosphorus pentoxide (although the a of the prefix penta-should actually not be omitted before a vowel: the IUPAC Red Book 2005 page 69 states, "The final vowels of multiplicative prefixes should not be elided (although "monoxide", rather than ...

  6. IUPAC nomenclature of inorganic chemistry 2005 - Wikipedia

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

    The number of ligands coordinating is indicated by the prefixes di-, tri-, tetra- penta- etc. for simple ligands or bis-, tris-, tetrakis-, etc. for complex ligands. For example: For example: [CoCl(NH 3 ) 5 ]Cl 2 pentaamminechloridocobalt(3+) chloride where ammine (NH 3 )precedes chloride.

  7. IUPAC nomenclature of organic chemistry - Wikipedia

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

    (The multiplier prefixes di-, tri-, etc. are not taken into consideration for grouping alphabetically. For example, ethyl comes before dihydroxy or dimethyl, as the "e" in "ethyl" precedes the "h" in "dihydroxy" and the "m" in "dimethyl" alphabetically. The "di" is not considered in either case).

  8. Polybrominated diphenyl ethers - Wikipedia

    en.wikipedia.org/wiki/Polybrominated_diphenyl_ethers

    The number of isomers for mono-, di-, tri-, tetra-, penta-, hexa-, hepta-, octa-, nona-, and decabromodiphenyl ethers are 3, 12, 24, 42, 46, 42, 24, 12, 3 and 1, respectively. [ 5 ] Lower-brominated PBDEs with 1–4 bromine atoms per molecule are regarded as more dangerous because they more efficiently bioaccumulate .

  9. Hydroxynaphthoquinone - Wikipedia

    en.wikipedia.org/wiki/Hydroxynaphthoquinone

    In this case the number n (which is between 1 and 6) is indicated by a multiplier prefix (mono-, di-, tri-, tetra-, penta-, or hexa-). The unqualified term "hydroxynaphthoquinone" usually means a derivative of 1,4-naphthoquinone .