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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.
Phenacyl bromide is the organic compound with the formula C 6 H 5 C(O)CH 2 Br. This colourless solid is a powerful lachrymator as well as a useful precursor to other organic compounds. It is prepared by bromination of acetophenone: [2] C 6 H 5 C(O)CH 3 + Br 2 → C 6 H 5 C(O)CH 2 Br + HBr. The compound was first reported in 1871. [3]
The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure. Units of solubility are given in grams of substance per 100 millilitres of water (g/(100 mL)), unless shown otherwise.
POCl 3 reacts with water to give hydrogen chloride and phosphoric acid: O=PCl 3 + 3 H 2 O → O=P(OH) 3 + 3 HCl. Intermediates in the conversion have been isolated, including pyrophosphoryl chloride, O(−P(=O)Cl 2) 2. [9] Upon treatment with excess alcohols and phenols, POCl 3 gives phosphate esters: O=PCl 3 + 3 ROH → O=P(OR) 3 + 3 HCl
In organic chemistry, a phenacyl group is an aromatic substituent that consists of a phenyl group attached to an acyl group. A molecule containing a phenacyl group has the formula RCH 2 (CO)C 6 H 5 and the structure shown to the right. Here, R denotes the remainder of the molecule; for instance, if R is Br, then the compound could be called ...
This is a list of common chemical compounds with chemical formulae and CAS numbers, indexed by formula. This complements alternative listing at list of inorganic compounds. There is no complete list of chemical compounds since by nature the list would be infinite.
Triphenylphosphine is produced industrially by the reaction between phosphorus trichlorid, chlorobenzene, and sodium: [13] PCl 3 + 3 PhCl + 6 Na → PPh 3 + 6 NaCl , where Ph = C 6 H 5 Under controlled conditions or especially with bulky R groups, similar reactions afford less substituted derivatives such as chlorodiisopropylphosphine .
The reaction of VX with concentrated aqueous sodium hydroxide results in two competing solvolysis reactions: cleavage of either the P–O or P–S esters. Although the P–S cleavage is the dominant pathway, the product of P–O bond cleavage is the toxic phosphonic thioester EA-2192 and both reactions are slow. [ 28 ]