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  2. Aniline - Wikipedia

    en.wikipedia.org/wiki/Aniline

    Aniline reacts with strong acids to form the anilinium (or phenylammonium) ion (C 6 H 5 −NH + 3). [ 20 ] Traditionally, the weak basicity of aniline is attributed to a combination of inductive effect from the more electronegative sp 2 carbon and resonance effects, as the lone pair on the nitrogen is partially delocalized into the pi system of ...

  3. Bromine water - Wikipedia

    en.wikipedia.org/wiki/Bromine_water

    Bromine water, Br 2. Bromine water is an oxidizing, intense brown mixture containing diatomic bromine (Br 2) dissolved in water (H 2 O). [1] It is often used as a reactive in chemical assays of recognition for substances which react with bromine in an aqueous environment with the halogenation mechanism, mainly unsaturated carbon compounds (carbon compounds with 1 or more double or triple bond(s)).

  4. N-Bromosuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Bromosuccinimide

    NBS reacts with alkenes in aqueous solvents to give bromohydrins. The preferred conditions are the portionwise addition of NBS to a solution of the alkene in 50% aqueous DMSO, DME, THF, or tert-butanol at 0 °C. [3] Formation of a bromonium ion and immediate attack by water gives strong Markovnikov addition and anti stereochemical selectivities ...

  5. Hofmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Hofmann_rearrangement

    The anion reacts with bromine in an α-substitution reaction to give an N-bromoamide. Base abstraction of the remaining amide proton gives a bromoamide anion. The bromoamide anion rearranges as the R group attached to the carbonyl carbon migrates to nitrogen at the same time the bromide ion leaves, giving an isocyanate.

  6. Bromine test - Wikipedia

    en.wikipedia.org/wiki/Bromine_test

    The formation of a brominated phenol (i.e. 2,4,6-tribromophenol) or aniline (i.e. 2,4,6-tribromoaniline) in form of a white precipitate indicates that the unknown was a phenol or aniline. The more unsaturated an unknown is, the more bromine it reacts with, and the less coloured the solution will appear. [1]

  7. Aniline (data page) - Wikipedia

    en.wikipedia.org/wiki/Aniline_(data_page)

    Aniline absorbs in the K (220 - 250 nm) and the B (250 - 290 nm) bands exhibited by benzenoid compounds. The K and B bands arise from π to π* transitions as a result of the a group containing multiple bond being attached to the benzene ring. When dissolved in ethanol, λ max for aniline is 230 nm, but in dilute aqueous acid λ max is 203 nm ...

  8. Cyanogen bromide - Wikipedia

    en.wikipedia.org/wiki/Cyanogen_bromide

    The carbon atom in cyanogen bromide is bonded to bromine by a single bond and to nitrogen by a triple bond (i.e. Br−C≡N). The compound is linear and polar, but it does not spontaneously ionize in water. It dissolves in both water and polar organic solvents.

  9. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    (Nonetheless, nitrogen tribromide is named as a bromide as it is analogous to the other nitrogen trihalides.) [4] Bromination of metals with Br 2 tends to yield lower oxidation states than chlorination with Cl 2 when a variety of oxidation states is available. Bromides can be made by reaction of an element or its oxide, hydroxide, or carbonate ...