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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]
CAS Number. 17642-31-8; 3D model . Interactive image; ChemSpider: 95710859; PubChem CID. 154735205; ... This page was last edited on 4 January 2025, at 10:50 (UTC).
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 ...
Tear gas in use in France 2007 Exploded tear gas canister in the air in Greece. Tear gas, also known as a lachrymatory agent or lachrymator (from Latin lacrima 'tear'), sometimes colloquially known as "mace" after the early commercial self-defense spray, is a chemical weapon that stimulates the nerves of the lacrimal gland in the eye to produce tears.
CAS number Ac 2 O 3: actinium(III) oxide: 12002-61-8 AgBF 4: Silver tetrafluoroborate: 14104-20-2 AgBr: silver bromide: 7785-23-1 AgBrO: silver hypobromite: AgBrO 2: silver bromite: AgBrO 3: silver bromate: 7783-89-3 AgBrO 4: silver perbromate: AgCl: silver chloride: 7783-90-6 AgCl 3 Cu 2: dicopper silver trichloride: 69569-03-5 AgClO 3: silver ...
Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75
NBS is commercially available. It can also be synthesized in the laboratory. To do so, sodium hydroxide and bromine are added to an ice-water solution of succinimide. The NBS product precipitates and can be collected by filtration. [2] Crude NBS gives better yield in the Wohl–Ziegler reaction. In other cases, impure NBS (slightly yellow in ...
[citation needed] More modern treatments explain the tight P–O bond as a combination of lone pair transfer from the phosphorus to the oxygen atom and a dative π back-bond that produces an effective [P +]-[O −] configuration. [7] Phosphoryl chloride exists as neutral POCl 3 molecules in the solid, liquid and gas states.