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  2. Sulfurous acid - Wikipedia

    en.wikipedia.org/wiki/Sulfurous_acid

    Sulfurous acid is commonly known to not exist in its free state, and due to this, it is stated in textbooks that it cannot be isolated in the water-free form. [4] However, the molecule has been detected in the gas phase in 1988 by the dissociative ionization of diethyl sulfite. [5]

  3. IUPAC nomenclature of organic chemistry - Wikipedia

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

    ChemAxon Name <> Structure – ChemAxon IUPAC (& traditional) name to structure and structure to IUPAC name software. As used at chemicalize.org; chemicalize.org A free web site/service that extracts IUPAC names from web pages and annotates a 'chemicalized' version with structure images. Structures from annotated pages can also be searched.

  4. 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)

  5. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    However, some compounds may have alternative names that are also accepted, known as the preferred IUPAC name which is generally taken from the common name of that compound. Preferably, the name should also represent the structure or chemistry of a compound. For example, the main constituent of white vinegar is CH 3 COOH, which is commonly ...

  6. Thiosulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Thiosulfuric_acid

    The structure of the conjugate base of thiosulfuric acid. [8] The isomer (O=) 2 S(−OH)(−SH) is more stable than the isomer (O=)(S=)S(−OH) 2 as established by Hartree–Fock/ab initio calculations with a 6-311 G** basis set and MP2 to MP4 refinements. [8] [clarification needed] The theoretically predicted structure conforms with the double ...

  7. Sulfoxylic acid - Wikipedia

    en.wikipedia.org/wiki/Sulfoxylic_acid

    The nomenclature for these molecules is not entirely standardized, and a wide variety of IUPAC-acceptable names are possible. For substances with the −OSOH group, one can use suffixes ‑oxy­sulfanol (preferred), ‑hydrogen sulfoxylate, or ‑oxy­sulfenic acid; or prefixes hydroxy­sulfanyl­oxy- (preferred) or sulfeno­oxy-.

  8. Sulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Sulfuric_acid

    Sulfuric acid (American spelling and the preferred IUPAC name) or sulphuric acid (Commonwealth spelling), known in antiquity as oil of vitriol, is a mineral acid composed of the elements sulfur, oxygen, and hydrogen, with the molecular formula H 2 SO 4. It is a colorless, odorless, and viscous liquid that is miscible with water. [7] Structure ...

  9. Bisulfite - Wikipedia

    en.wikipedia.org/wiki/Bisulfite

    The bisulfite ion (IUPAC-recommended nomenclature: hydrogensulfite) is the ion HSO − 3. Salts containing the HSO − 3 ion are also known as "sulfite lyes". [1] Sodium bisulfite is used interchangeably with sodium metabisulfite (Na 2 S 2 O 5). Sodium metabisulfite dissolves in water to give a solution of Na + HSO − 3. Na 2 S 2 O 5 + H 2 O ...