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  1. en.wikipedia.org › wiki › BromobenzeneBromobenzene - Wikipedia

    Bromobenzene is an aryl bromide and the simplest of the bromobenzenes, consisting of a benzene ring substituted with one bromine atom. Its chemical formula is C6H5Br. It is a colourless liquid although older samples can appear yellow. It is a reagent in organic synthesis .

  2. Bromobenzene | C6H5Br | CID 7961 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

  3. Structure, properties, spectra, suppliers and links for: Bromobenzene, 108-86-1, 52753-63-6.

  4. CAS Registry Number: 108-86-1. Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file. The 3d structure may be viewed using Java or Javascript . Other names: Bromobenzene; Monobromobenzene; Phenyl bromide; 1-Bromobenzene; NCI-C55492; UN 2514. Permanent link for this species.

  5. The 3D chemical structure image of BROMOBENZENE is based on the ball-and-stick model which displays both the three-dimensional position of the atoms and the bonds between them. The radius of the spheres is therefore smaller than the rod lengths in order to provide a clearer view of the atoms and bonds throughout the chemical structure model of ...

  6. The simplest member of the class of bromobenzenes, that is benzene in which a single hydrogen has been substituted by a bromine. A liquid at room temperature (m.p. −30°C; b.p. 760 156°C), it is used as a solvent, particularly for large-scale crystallisations, and for the introduction of phenyl groups in organic synthesis. Stars.

  7. Video transcript. I mentioned in the last video that 99% of the aromatic compounds that you'll see in a chemistry or organic chemistry class is either going to be benzene or a molecule derived from benzene. So what I want to do in this video is just familiarize you with some of these molecules and how to name them.

  8. You can recognize the aromatic compounds in this text by the presence of one or more benzene rings in their structure. Some representative aromatic compounds and their uses are listed in Table 13.8.1 13.8. 1, where the benzene ring is represented as C 6 H 5.

  9. The bromination of benzene is an example of an electrophilic aromatic substitution reaction. In this reaction, the electrophile (bromine) forms a sigma bond to the benzene ring, yielding an intermediate. Then, a proton is removed from the intermediate to form a substituted benzene ring. Created by Sal Khan. Questions.

  10. Bromobenzene, a chemical intermediate, is both a heptotoxicant and a nephrotoxicant. Bromobenzene-induced nephrotoxicity is characterized by glucosuria, enzymuria, proteinuria, elevated BUN concentration and kidney weight, and proximal tubular necrosis with the S 3 segment exhibiting the greatest damage.

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