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2. Organobromine chemistry - Wikipedia

   en.wikipedia.org/wiki/Organobromine_chemistry

   RCH=CH 2 + HBr → RCHBrCH 3. Under free radical conditions, the direction of the addition can be reversed. Free-radical addition is used commercially for the synthesis of 1-bromoalkanes, precursors to tertiary amines and quaternary ammonium salts. 2-Phenethyl bromide (C 6 H 5 CH 2 CH 2 Br) is produced via this route from styrene.

3. 2-Phenylethyl bromide - Wikipedia

   en.wikipedia.org/wiki/2-Phenylethyl_bromide

   2-Phenylethyl bromide is an organobromide with the formula C 6 H 5 CH 2 CH 2 Br. It is a colorless liquid, although older samples appear yellow. Analogous to the preparation of most 1-bromoalkanes, it is prepared by free-radical addition of hydrogen bromide to styrene. These conditions lead to anti-Markovnikov addition, giving the 1-bromo ...

4. Bromine compounds - Wikipedia

   en.wikipedia.org/wiki/Bromine_compounds

   Silver bromide (AgBr). Nearly all elements in the periodic table form binary bromides. The exceptions are decidedly in the minority and stem in each case from one of three causes: extreme inertness and reluctance to participate in chemical reactions (the noble gases, with the exception of xenon in the very unstable XeBr 2; extreme nuclear instability hampering chemical investigation before ...

5. Substituted phenethylamine - Wikipedia

   en.wikipedia.org/wiki/Substituted_phenethylamine

   Substituted phenethylamines (or simply phenethylamines) are a chemical class of organic compounds that are based upon the phenethylamine structure; [note 1] the class is composed of all the derivative compounds of phenethylamine which can be formed by replacing, or substituting, one or more hydrogen atoms in the phenethylamine core structure with substituents.

6. Bromomethane - Wikipedia

   en.wikipedia.org/wiki/Bromomethane

   Bromomethane, commonly known as methyl bromide, is an organobromine compound with formula C H 3 Br. This colorless, odorless, nonflammable gas is produced both industrially and biologically. This colorless, odorless, nonflammable gas is produced both industrially and biologically.

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   Get lifestyle news, with the latest style articles, fashion news, recipes, home features, videos and much more for your daily life from AOL.

8. Methylenetriphenylphosphorane - Wikipedia

   en.wikipedia.org/wiki/Methylenetriphenylphosphorane

   The estimated pK a of this carbon acid is near 15. [2] Potassium tert-butoxide has been used in place of butyl lithium. [3] Sodium amide has also been used a base. [4] Methylenetriphenylphosphorane is used to replace oxygen centres in aldehydes and ketones with a methylene group, i.e., a methylenation: R 2 CO + Ph 3 PCH 2 → R 2 C=CH 2 + Ph 3 PO

9. Thousands of liters of chemicals dumped into Brazilian river ...

   www.aol.com/thousands-liters-chemicals-dumped...

   President Luiz Inácio Lula da Silva sent his condolences to the families of the victims in a post to social media Monday, and said his government will support local authorities in dealing with ...