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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]
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 ...
Ca(NO 3) 2: calcium nitrate: 10124-37-5 Ca(NO 3) 2 · 4H 2 O: Calcium nitrate tetrahydrate: 13477-34-4 Ca(NbO 3) 2: calcium metaniobate: CaO: quicklime calcium oxide burnt lime: 1305-78-8 Ca(OH) 2: calcium hydroxide slaked lime: 1305-62-0 CaO 2: calcium peroxide: 1305-79-9 CaP: calcium monophosphide: 39373-03-0 CaS: calcium sulfide hepar ...
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 Wittig reaction or Wittig olefination is a chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide called a Wittig reagent. Wittig reactions are most commonly used to convert aldehydes and ketones to alkenes.
Zinc nitrate is usually prepared by dissolving zinc metal, zinc oxide, or related materials in nitric acid: Zn + 2 HNO 3 → Zn(NO 3) 2 + H 2 ZnO + 2 HNO 3 → Zn(NO 3) 2 + H 2 O. These reactions are accompanied by the hydration of the zinc nitrate. The anhydrous salt arises by the reaction of anhydrous zinc chloride with nitrogen dioxide: [1]
The Perkow reaction is a competing reaction pathway for α-bromo- and α-chloroketones. Under the reaction conditions a mixture of the Perkow product and the normal Arbuzov product occur, usually favoring the Perkow product by a significant amount. Using higher temperatures during the reaction can lead to favoring of the Arbuzov product.
This difference in reactivity can be exploited to selectively couple an aryl iodide but not an aryl bromide, by performing the reaction at room temperature. [9] An example is the symmetrical Sonogashira coupling of two equivalents of 1-bromo-4-iodobenzene with trimethylsilylacetylene (with the trimethylsilyl group removed in-situ ) to form bis ...