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  2. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    A halogen addition reaction is a simple organic reaction where a halogen molecule is added to the carbon–carbon double bond of an alkene functional group. [1] The general chemical formula of the halogen addition reaction is: C=C + X 2 → X−C−C−X (X represents the halogens bromine or chlorine, and in this case, a solvent could be CH 2 ...

  3. Halogen - Wikipedia

    en.wikipedia.org/wiki/Halogen

    The halogens (/ ˈ h æ l ə dʒ ə n, ˈ h eɪ-,-l oʊ-,-ˌ dʒ ɛ n / [1] [2] [3]) are a group in the periodic table consisting of six chemically related elements: fluorine (F), chlorine (Cl), bromine (Br), iodine (I), and the radioactive elements astatine (At) and tennessine (Ts), though some authors [4] would exclude tennessine as its chemistry is unknown and is theoretically expected to ...

  4. Homestake experiment - Wikipedia

    en.wikipedia.org/wiki/Homestake_experiment

    The Homestake experiment (sometimes referred to as the Davis experiment or Solar Neutrino Experiment and in original literature called Brookhaven Solar Neutrino Experiment or Brookhaven 37 Cl (Chlorine) Experiment) [1] was an experiment headed by astrophysicists Raymond Davis, Jr. and John N. Bahcall in the late 1960s.

  5. Chlorine - Wikipedia

    en.wikipedia.org/wiki/Chlorine

    Chlorine is the second halogen, being a nonmetal in group 17 of the periodic table. Its properties are thus similar to fluorine, bromine, and iodine, and are largely intermediate between those of the first two. Chlorine has the electron configuration [Ne]3s 2 3p 5, with the seven electrons in the third and outermost shell acting as its valence ...

  6. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    Organochlorine chemistry is concerned with the properties of organochlorine compounds, or organochlorides, organic compounds that contain one or more carbon–chlorine bonds. [1] The chloroalkane class (alkanes with one or more hydrogens substituted by chlorine) includes common examples. The wide structural variety and divergent chemical ...

  7. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    Halogenation of saturated hydrocarbons is a substitution reaction. The reaction typically involves free radical pathways. The regiochemistry of the halogenation of alkanes is largely determined by the relative weakness of the C–H bonds. This trend is reflected by the faster reaction at tertiary and secondary positions.

  8. Interhalogen - Wikipedia

    en.wikipedia.org/wiki/Interhalogen

    It has the same molecular shape as chlorine trifluoride. Iodine trifluoride (IF 3) is a yellow solid that decomposes above −28 °C. It can be synthesised from the elements, but care must be taken to avoid the formation of IF 5. F 2 attacks I 2 to yield IF 3 at −45 °C in CCl 3 F. Alternatively, at low temperatures, the fluorination reaction

  9. Chlorine oxide - Wikipedia

    en.wikipedia.org/wiki/Chlorine_oxide

    Chlorine and oxygen can bond in a number of ways: chlorine monoxide radical, ClO•, chlorine (II) oxide radical; chloroperoxyl radical, ClOO•, chlorine (II) peroxide radical; chlorine dioxide, ClO 2, chlorine (IV) oxide; chlorine trioxide radical, ClO 3 •, chlorine (VI) oxide radical; chlorine tetroxide radical, ClO 4 •, chlorine (VII ...