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  2. 2-Bromohexane - Wikipedia

    en.wikipedia.org/wiki/2-Bromohexane

    2-Bromohexane is the organobromine compound with the formula CH 3 CH(Br)(CH 2) 3 CH 3. It is a colorless liquid. The compound is chiral. Most 2-bromoalkanes are prepared by addition of hydrogen bromide to the 1-alkene. Markovnikov addition proceeds in the absence of free-radicals, i.e. give the 2-bromo derivatives. [2]

  3. C6H13Br - Wikipedia

    en.wikipedia.org/wiki/C6H13Br

    2-Bromohexane Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .

  4. 1-Fluorohexane - Wikipedia

    en.wikipedia.org/wiki/1-Fluorohexane

    The compound is primarily used in the field of organic chemistry as a reagent or solvent. Also, 1-fluorohexane is used in physical chemistry as a model compound for understanding the physico-chemical properties of fluorinated hydrocarbons.

  5. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    1-Bromobutane is the organobromine compound with the formula CH 3 (CH 2) 3 Br. It is a colorless liquid, although impure samples appear yellowish. It is insoluble in water, but soluble in organic solvents. It is primarily used as a source of the butyl group in organic synthesis. It is one of several isomers of butyl bromide.

  6. 1-Bromohexane - Wikipedia

    en.wikipedia.org/wiki/1-Bromohexane

    1-Bromohexane undergoes reactions expected of simple alkyl bromides. It can form Grignard reagents . [ 3 ] It reacts with potassium fluoride to give the corresponding fluorocarbons .

  7. Category:Bromoalkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Bromoalkanes

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  8. Bromocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Bromocyclohexane

    Properties Chemical formula. C 6 H 11 Br Molar mass: 163.06 g/mol Appearance ... is an organic compound with the chemical formula (CH 2) 5 CHBr. Uses and reactions

  9. Phosphonium - Wikipedia

    en.wikipedia.org/wiki/Phosphonium

    Wittig reagents are used in organic synthesis. They are derived from phosphonium salts. A strong base such as butyllithium or sodium amide is required for the deprotonation: [Ph 3 P + CH 2 R]X − + C 4 H 9 Li → Ph 3 P=CHR + LiX + C 4 H 10. One of the simplest ylides is methylenetriphenylphosphorane (Ph 3 P=CH 2). [6]