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Oxalic acid is an organic acid with the systematic name ethanedioic acid and chemical formula HO−C(=O)−C(=O)−OH, also written as (COOH) 2 or (CO 2 H) 2 or H 2 C 2 O 4. It is the simplest dicarboxylic acid. It is a white crystalline solid that forms a colorless solution in water.
2 H 2 O ⇌ H 3 O + (aq) + OH − (aq) with a dissociation constant, K w defined as = [+] [] where [H +] stands for the concentration of the aqueous hydronium ion and [OH −] represents the concentration of the hydroxide ion. This equilibrium needs to be taken into account at high pH and when the solute concentration is extremely low.
In chemistry, a hydroxy or hydroxyl group is a functional group with the chemical formula −OH and composed of one oxygen atom covalently bonded to one hydrogen atom. In organic chemistry , alcohols and carboxylic acids contain one or more hydroxy groups.
Originally focusing on contract research and development work in the areas of metals and material science, Battelle is now an international science and technology enterprise that explores emerging areas of science, develops and commercializes technology, and manages laboratories for customers.
The polymeric compounds M(OH) 2 and M(OH) 3 are in general prepared by increasing the pH of an aqueous solutions of the corresponding metal cations until the hydroxide precipitates out of solution. On the converse, the hydroxides dissolve in acidic solution. Zinc hydroxide Zn(OH) 2 is amphoteric, forming the tetrahydroxidozincate ion Zn(OH) 2−
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When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...
For many years, beginning in 1909, the offices of Chemical Abstracts were housed in various places on the Columbus, Ohio campus of Ohio State University, including McPherson Laboratory and Watts Hall. [14] In 1965, CAS moved to a new 50-acre (200,000 m 2) site on the west bank of the Olentangy River, just north of The Ohio State campus.
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