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A supersaturated solution of sodium acetate in water is supplied with a device to initiate crystallization, a process that releases substantial heat. Solubility from CRC Handbook. Sodium acetate trihydrate crystals melt at 58–58.4 °C (136.4–137.1 °F), [12] [13] and the liquid sodium acetate dissolves in the released water of crystallization.
1% and 2% uranyl acetate solutions are used as an indicator, and a titrant in stronger concentrations in analytical chemistry, as it forms an insoluble salt with sodium (the vast majority of sodium salts are water-soluble). Uranyl acetate solutions show evidence of being sensitive to light, especially UV, and will precipitate if exposed.
Acetate is the ion resulting from loss of H + from acetic acid. The name "acetate" can also refer to a salt containing this anion, or an ester of acetic acid. [11] (The symbol Ac for the acetyl functional group is not to be confused with the symbol Ac for the element actinium; context prevents confusion among organic chemists).
A commonly encountered acetate in the home is sodium acetate, a white solid that can be prepared by combining vinegar and sodium bicarbonate ("bicarbonate of soda"): CH 3 COOH + NaHCO 3 → CH 3 COO − Na + + H 2 O + CO 2. Transition metals can be complexed by acetate. Examples of acetate complexes include chromium(II) acetate and basic zinc ...
Uranyl zinc acetate (ZnUO 2 (CH 3 COO) 4) is a compound of uranium.. Uranyl zinc acetate is used as a laboratory reagent in the determination of sodium concentrations of solutions using a method of quantitatively precipitating sodium with uranyl zinc acetate and gravimetrically determining the sodium as uranyl zinc sodium acetate, (UO 2) 3 ZnNa(CH 3 CO 2) 9 ·6H 2 O.
Sodium fluoroacetate, also known as compound 1080, is an organofluorine chemical compound with the chemical formula F C H 2 CO 2 Na. It is the sodium salt of fluoroacetic acid. It contains sodium cations Na + and fluoroacetate anions FCH 2 CO − 2. This colourless salt has a taste similar to that of table salt (sodium chloride) and is used as ...
This page was last edited on 30 September 2023, at 19:07 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
These investigations used acetic acid as the solvent and demonstrated that sodium acetate behaves as a base under these conditions. [28] [29] This observation is consistent with Brønsted–Lowry acid–base theory published in 1923, [30] but cannot be explained under older Arrhenius theory approaches.
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