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  2. Bromobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromobenzene

    Bromobenzene is prepared by the action of bromine on benzene in the presence of Lewis acid catalysts such as aluminium chloride or ferric bromide. [3] Bromobenzene is used to introduce a phenyl group into other compounds. One method involves its conversion to the Grignard reagent, phenylmagnesium bromide.

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

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

    Toggle the table of contents. List of boiling and freezing information of solvents. ... Bromobenzene: 1.49 156.0 6.26 –30.6 Camphor: 204.0 5.95 179 –40 K f [2]

  4. List of cooling baths - Wikipedia

    en.wikipedia.org/wiki/List_of_cooling_baths

    Bromobenzene-30 Dry ice: m-Toluidine-32 Dry ice: 3-Heptanone-38 Ice: Calcium chloride hexahydrate -40 1 to 0.8 ratio of salt to ice. Dry ice: Acetonitrile-41 Dry ice: Pyridine-42 Dry ice: Cyclohexanone-46 Dry ice: m-Xylene-47 Dry ice: Diethyl carbitol-52 Dry ice: n-Octane-56 Dry ice: Diisopropyl ether-60 Dry ice: Chloroform-61 Liquid N 2 ...

  5. 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

  6. 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]

  7. Van der Waals constants (data page) - Wikipedia

    en.wikipedia.org/wiki/Van_der_Waals_constants...

    The following table lists the Van der Waals constants (from the Van der Waals equation) for a number of common gases and volatile liquids. [ 1 ] To convert from L 2 b a r / m o l 2 {\displaystyle \mathrm {L^{2}bar/mol^{2}} } to L 2 k P a / m o l 2 {\displaystyle \mathrm {L^{2}kPa/mol^{2}} } , multiply by 100.

  8. Von Richter reaction - Wikipedia

    en.wikipedia.org/wiki/Von_Richter_reaction

    The reaction below shows the classic example of the conversion of p-bromonitrobenzene into m-bromobenzoic acid. [4]Übersichtsreaktion der Von-Richter-Reaktion. The reaction is a type of nucleophilic aromatic substitution. [4]

  9. 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"