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  2. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Download as PDF; Printable version ... Solvent Density (g cm-3) Boiling point (°C) K b (°C⋅kg /mol) Freezing point (°C) K f ... Bromobenzene: 1.49 156.0 6.26 ...

  3. Bromobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromobenzene

    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 C 6 H 5 Br . It is a colourless liquid although older samples can appear yellow.

  4. Bromobenzenes - Wikipedia

    en.wikipedia.org/wiki/Bromobenzenes

    Bromobenzenes may be carboxylated into carboxylic acids using carbon monoxide.The reaction takes place in a two-phase mixture of p-xylene and water as solvent, in the presence of catalytic PdCl

  5. Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Bromobenzaldehyde

    Density and phase: 1.585 g/ml, liquid 1.587 g/ml, liquid solid Solubility in water: practically insoluble Melting point: 16–19 °C 18–21 °C 57 °C Boiling point: 230 °C 233–236 °C 255–258 °C

  6. Category:Bromobenzene compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Bromobenzene...

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  7. Category:Bromobenzenes - Wikipedia

    en.wikipedia.org/wiki/Category:Bromobenzenes

    If the benzene ring contains other substituents, it belongs in Category:Bromobenzene derivatives The main article for this category is Bromobenzenes . Pages in category "Bromobenzenes"

  8. 1,2,4,5-Tetrabromobenzene - Wikipedia

    en.wikipedia.org/wiki/1,2,4,5-Tetrabromobenzene

    1,2,4,5-Tetrabromobenzene is an aryl bromide and a four-substituted bromobenzene with the formula C 6 H 2 Br 4. It is one of three isomers of tetrabromobenzene. The compound is a white solid. 1,2,4,5-Tetrabromobenzene is an important metabolite of the flame retardant hexabromobenzene. [1]

  9. Benzyl bromide - Wikipedia

    en.wikipedia.org/wiki/Benzyl_bromide

    Benzyl bromide is used in organic synthesis for the introduction of the benzyl groups when the less expensive benzyl chloride is insufficiently reactive. [6] [7] Benzylations are often achieved in the presence of catalytic amounts of sodium iodide, which generates the more reactive benzyl iodide in situ. [3]