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  2. Nucleophilic aromatic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_aromatic...

    free radical S RN 1 mechanism; ANRORC mechanism; Vicarious nucleophilic substitution; The S N Ar mechanism is the most important of these. Electron withdrawing groups activate the ring towards nucleophilic attack. For example if there are nitro functional groups positioned ortho or para to the halide leaving group, the S N Ar mechanism is favored.

  3. Cyanation - Wikipedia

    en.wikipedia.org/wiki/Cyanation

    Nickel-catalyzed cyanations avoid the use of precious metals, and can take advantage of benzyl cyanide or acetonitrile as a cyanide source, via reductive C-C bond cleavage: [9] Sandmeyer cyanation is a means of converting aniline derivatives to benzonitriles. [ 10 ]

  4. 4-Bromoaniline - Wikipedia

    en.wikipedia.org/wiki/4-bromoaniline

    4-Bromoaniline is a compound where an aniline molecule is substituted with a bromine atom on the para position. Commercially available, this compound may be used as a building block, e.g. in the preparation of monobrominated biphenyl via the Gomberg-Bachmann reaction .

  5. 1,3,5-Tribromobenzene - Wikipedia

    en.wikipedia.org/wiki/1,3,5-Tribromobenzene

    Brominating aniline with elemental bromine gives 2,4,6-tribromoaniline. This is then diazotized, then reacted with ethanol to replace the diazonium group with hydrogen, forming 1,3,5-tribromobenzene. [3] It has also been prepared by these methods: [3] replacement of the amino group of 3,5-dibromoaniline with bromine

  6. 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.

  7. Sandmeyer reaction - Wikipedia

    en.wikipedia.org/wiki/Sandmeyer_reaction

    In numerous variants that have been developed, other transition metal salts, including copper(II), iron(III) and cobalt(III) have also been employed. [7] Due to its wide synthetic applicability, the Sandmeyer reaction, along with other transformations of diazonium compounds, is complementary to electrophilic aromatic substitution .

  8. The Top 10 Deadliest Animals In The World - AOL

    www.aol.com/top-10-deadliest-animals-world...

    Animals are all around us. Because of their proximity, many people take for granted how truly dangerous some animals really are. Let’s discuss the 10 most dangerous animals in the world ranked ...

  9. Transition metal - Wikipedia

    en.wikipedia.org/wiki/Transition_metal

    Late transition metals are on the right side of the d-block, from group 8 to 11 (or 12, if they are counted as transition metals). In an alternative three-way scheme, groups 3, 4, and 5 are classified as early transition metals, 6, 7, and 8 are classified as middle transition metals, and 9, 10, and 11 (and sometimes group 12) are classified as ...