Depending on the specific positions of the hydrogen atoms that are replaced by bromine, different isomeric products can form. For example, α- and β-bromination can occur, leading to different positional isomers.
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Cyclohexanone, 2-bromo-3-methyl-6-(1-methylethyl)-, (2R,3R,6S)-
(2Z,4Z)-5-(4-Hydroxy-2,6,6-trimethyl-cyclohex-1-enyl)-3-methyl-penta-2,4-dienal
(4S,6S,8S,10S)-6,8,10-tris(tert-butyldimethylsilyloxy)pentacos-1-en-4-yl (E)-3-phenylacrylate
5,5''-bis(mesityl(1H-pyrrol-2-yl)methyl)-2,2':5',2''-terthiophene
7-methoxy-3-(4-methoxyphenyl)-1H-isochromen-1-one
6-hydroxyketamine
[(isopropyl)2PB(phenyl)]2-diyl
(3R,6R,7S)-8-Benzyloxy-6-hydroxy-3,7-dimethyl-octanoic acid methyl ester
3-BENZYLOXY-1,1,1-TRIFLUORO-PROPAN-2-ONE
