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  2. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    In chemistry, an alcohol (from Arabic al-kuḥl 'the kohl'), [2] is a type of organic compound that carries at least one hydroxyl (−OH) functional group bound to a saturated carbon atom. [3] [4] Alcohols range from the simple, like methanol and ethanol, to complex, like sugar alcohols and cholesterol. The presence of an OH group strongly ...

  3. -ol - Wikipedia

    en.wikipedia.org/wiki/-ol

    The IUPAC name of alcohols can derive from the following rules: Identify the longest carbon chain, and number each carbon. Name the base alkane according to the organic nomenclature rules. Identify the hydroxyl group and which carbon it is on. To be alcohol, the -OH must be bonded to a carbon.

  4. Primary alcohol - Wikipedia

    en.wikipedia.org/wiki/Primary_alcohol

    A primary alcohol is an alcohol in which the hydroxy group is bonded to a primary carbon atom. It can also be defined as a molecule containing a “–CH 2 OH” group. [ 1 ] In contrast, a secondary alcohol has a formula “–CHROH” and a tertiary alcohol has a formula “–CR 2 OH”, where “R” indicates a carbon-containing group.

  5. List of alkanols - Wikipedia

    en.wikipedia.org/wiki/List_of_alkanols

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  6. IUPAC nomenclature of organic chemistry - Wikipedia

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

    In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended [1] [2] by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry (informally called the Blue Book). [3]

  7. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    Chemical nomenclature however (with IUPAC nomenclature as the best example) is necessarily more restrictive: Its purpose is to standardize communication and practice so that, when a chemical term is used it has a fixed meaning relating to chemical structure, thereby giving insights into chemical properties and derived molecular functions. These ...

  8. Geminal diol - Wikipedia

    en.wikipedia.org/wiki/Geminal_diol

    Geminal diols are a subclass of the diols, which in turn are a special class of alcohols. Most of the geminal diols are considered unstable. The simplest geminal diol is methanediol CH 4 O 2 or H 2 C(OH) 2. Other examples are: dihydroxymalinic acid (HOOC) 2 C(OH) 2; decahydroxycyclopentane (C(OH) 2) 5; chloral hydrate (Cl 3 C)HC(OH) 2.

  9. Category:Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Category:Chemical_nomenclature

    International Nomenclature of Cosmetic Ingredients; International Union of Biochemistry and Molecular Biology; International Union of Pure and Applied Chemistry; IUPAC Color Books; IUPAC Inorganic Chemistry Division; IUPAC nomenclature for organic chemical transformations; IUPAC nomenclature of inorganic chemistry; IUPAC nomenclature of ...