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  2. 3-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/3-Bromopentane

    151.047 g·mol −1 Appearance colorless liquid Density: 1.208 g mL −1 [2] Boiling point: 118–119 °C; 244–246 °F; 391–392 K Hazards GHS labelling: Pictograms.

  3. Bromopentane - Wikipedia

    en.wikipedia.org/wiki/Bromopentane

    1-Bromopentane; 2-Bromopentane [1] (chiral) 3-Bromopentane; There are four isomers of monobromopentane based on 2-methylbutane: 1-Bromo-2-methylbutane (chiral) 1-Bromo-3-methylbutane; 2-Bromo-2-methylbutane; 2-Bromo-3-methylbutane (chiral) 2,2-Dimethylpropane has only one monobrominated derivative, 1-bromo-2,2-dimethylpropane, also known as ...

  4. Iodobenzene - Wikipedia

    en.wikipedia.org/wiki/Iodobenzene

    Iodobenzene reacts with chlorine to give the complex, iodobenzene dichloride, [4] which is used as a solid source of chlorine. Iodobenzene can also serve as a substrate for the Sonogashira coupling , Heck reaction , and other metal-catalyzed couplings.

  5. Dehalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehalogenation

    Such reactions give alkenes in the case of vicinal alkyl dihalides: [2] R 2 C(X)C(X)R 2 + M → R 2 C=CR 2 + MX 2. Most desirable from the perspective of remediation are dehalogenations by hydrogenolysis, i.e. the replacement of a C−X bond by a C−H bond. Such reactions are amenable to catalysis: R−X + H 2 → R−H + HX

  6. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    Monobromotoluene isomers [1] [2] [3] Common name Structure Systematic name: 1-bromo-2-methylbenzene 1-bromo-3-methylbenzene 1-bromo-4-methylbenzene Molecular formula: C 7 H 7 Br (C 6 H 4 BrCH 3) Molar mass: 171.03 g/mol Appearance colorless liquid colorless liquid white crystalline solid CAS number [95-46-5] [591-17-3]

  7. 1-Bromo-4-iodobenzene - Wikipedia

    en.wikipedia.org/wiki/1-bromo-4-iodobenzene

    1-Bromo-4-iodobenzene is a mixed aryl halide (aryl bromide and aryl iodide) with the formula BrC 6 H 4 I. [2] Preparation. In one laboratory route to 1-bromo-4 ...

  8. Organobromine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organobromine_chemistry

    Bromine is more electronegative than carbon (2.9 vs 2.5). Consequently, the carbon in a carbon–bromine bond is electrophilic, i.e. alkyl bromides are alkylating agents. [2] Carbon–halogen bond strengths, or bond dissociation energies are of 115, 83.7, 72.1, and 57.6 kcal/mol for bonded to fluorine, chlorine, bromine, or iodine, respectively ...

  9. Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Bromobenzaldehyde

    2-Bromobenzaldehyde [1] 3-Bromobenzaldehyde [2] 4-Bromobenzaldehyde [3] [4] Structure Molecular formula: C 7 H 5 BrO (BrC 6 H 4 COH) Molar mass: 185.020 g/mol Appearance colorless liquid colorless liquid white solid CAS number [6630-33-7] [3132-99-8] [1122-91-4] Properties Density and phase: 1.585 g/ml, liquid 1.587 g/ml, liquid solid ...