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  2. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    The facility of halogenation is influenced by the halogen. Fluorine and chlorine are more electrophilic and are more aggressive halogenating agents. Bromine is a weaker halogenating agent than both fluorine and chlorine, while iodine is the least reactive of them all.

  3. Hospital Sisters Health System - Wikipedia

    en.wikipedia.org/wiki/Hospital_Sisters_Health_System

    Hospital Sisters Health System, or HSHS, is a non-profit healthcare system headquartered in Springfield, Illinois. HSHS operates a network of 15 hospitals and other healthcare facilities throughout the midwestern U.S. states of Illinois , and Wisconsin .

  4. Halogen - Wikipedia

    en.wikipedia.org/wiki/Halogen

    The chemical reactivity of halogen atoms depends on both their point of attachment to the lead and the nature of the halogen. Aromatic halogen groups are far less reactive than aliphatic halogen groups, which can exhibit considerable chemical reactivity. For aliphatic carbon-halogen bonds, the C-F bond is the strongest and usually less ...

  5. Hydrogenated starch hydrolysates - Wikipedia

    en.wikipedia.org/wiki/Hydrogenated_starch_hydro...

    Hydrogenated starch hydrolysates (HSHs), also known as polyglycitol syrup (INS 964), are mixtures of several sugar alcohols (a type of sugar substitute). Hydrogenated starch hydrolysates were developed by the Swedish company Lyckeby Starch in the 1960s. [1]

  6. Halogen bond - Wikipedia

    en.wikipedia.org/wiki/Halogen_bond

    Halogen bonds occur when a halogen atom is electrostatically attracted to a partial negative charge. Necessarily, the atom must be covalently bonded in an antipodal σ-bond ; the electron concentration associated with that bond leaves a positively charged "hole" on the other side. [7]

  7. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    In primary (1°) haloalkanes, the carbon that carries the halogen atom is only attached to one other alkyl group. An example is chloroethane (CH 3 CH 2 Cl). In secondary (2°) haloalkanes, the carbon that carries the halogen atom has two C–C bonds. In tertiary (3°) haloalkanes, the carbon that carries the halogen atom has three C–C bonds.

  8. Interhalogen - Wikipedia

    en.wikipedia.org/wiki/Interhalogen

    Typically, interhalogen bonds are more reactive than diatomic halogen bonds—because interhalogen bonds are weaker than diatomic halogen bonds, except for F 2. If interhalogens are exposed to water, they convert to halide and oxyhalide ions. With BrF 5, this reaction can be explosive.

  9. Haloacetic acids - Wikipedia

    en.wikipedia.org/wiki/Haloacetic_acids

    Haloacetic acids or HAAs are carboxylic acids in which one or more halogen atoms take the place of hydrogen atoms in the methyl group of acetic acid.Those acids have a general chemical formula X 1 X 2 X 3 C−CO 2 H, where X is hydrogen or halogen, and at least one X is a halogen.