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Anhydrous cobalt(II) fluoride. Cobalt(II) fluoride is a chemical compound with the formula (CoF 2).It is a pink crystalline solid compound [1] [2] which is antiferromagnetic at low temperatures (T N =37.7 K) [3] The formula is given for both the red tetragonal crystal, (CoF 2), and the tetrahydrate red orthogonal crystal, (CoF 2 ·4H 2 O).
Cobalt(II) nitrate exists in the anhydrous form and the hydrate form, of which the hexahydrate is the most common. Cobalt nitrate hexahydrate (Co(NO 3 ) 2 ·6H 2 O) is a red deliquescence crystal that is easily soluble in water, [ 12 ] and its molecule contains cobalt(II) hydrated ions ([Co(H 2 O) 6 ] 2+ ) and free nitrate ions. [ 13 ]
The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...
Where an acid has both a systematic and a common name (like CH 3 COOH, for example, which is known as both acetic acid and as ethanoic acid), its salts can be named from either parent name. Thus, KCH 3 CO 2 can be named as potassium acetate or as potassium ethanoate.
Skeletal structural formula of Vitamin B 12.Many organic molecules are too complicated to be specified by a molecular formula.. The structural formula of a chemical compound is a graphic representation of the molecular structure (determined by structural chemistry methods), showing how the atoms are possibly arranged in the real three-dimensional space.
Chemical formulae as described here are distinct from the far more complex chemical systematic names that are used in various systems of chemical nomenclature. For example, one systematic name for glucose is (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal. This name, interpreted by the rules behind it, fully specifies glucose's structural formula ...
An organic acid is an organic compound with acidic properties. The most common organic acids are the carboxylic acids , whose acidity is associated with their carboxyl group –COOH. Sulfonic acids , containing the group –SO 2 OH, are relatively stronger acids.
Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.