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Oxidation of the salt gives tetraacetylethane. [2]With metal salts, it reacts to give metal acetylacetonate complexes.. Alkylation of sodium acetylacetonate can result in both O-alkylation and C-alkylation.
Unlike some types of heat packs, such as those dependent upon irreversible chemical reactions, a sodium acetate heat pack can be easily reused by immersing the pack in boiling water for a few minutes, until the crystals are completely dissolved, and allowing the pack to slowly cool to room temperature.
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
The crystal structure of sodium ethoxide has been determined by X-ray crystallography.It consists of layers of alternating Na + and O − centres with disordered ethyl groups covering the top and bottom of each layer.
In organic chemistry, a carbonyl group is a functional group with the formula C=O, composed of a carbon atom double-bonded to an oxygen atom, and it is divalent at the C atom. It is common to several classes of organic compounds (such as aldehydes, ketones and carboxylic acid), as part of many larger functional groups. A compound containing a ...
A salt metathesis reaction is a chemical process involving the exchange of bonds between two reacting chemical species which results in the creation of products with similar or identical bonding affiliations. [1] This reaction is represented by the general scheme: + +
Sodium percarbonate or sodium carbonate peroxide is a chemical substance with empirical formula Na 2 H 3 C 2 O 6. It is an adduct of sodium carbonate ("soda ash" or "washing soda") and hydrogen peroxide (that is, a perhydrate) whose formula is more properly written as 2 Na 2 CO 3 · 3 H 2 O 2. It is a colorless, crystalline, hygroscopic and ...
Sodium methoxide is a routinely used base in organic chemistry, applicable to the synthesis of numerous compounds ranging from pharmaceuticals to agrichemicals. [4] As a base, it is employed in dehydrohalogenations and various condensations. [5] It is also a nucleophile for the production of methyl ethers. [6]