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  2. 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.

  3. Neutralization (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Neutralization_(chemistry)

    An example of a base being neutralized by an acid is as follows. Ba(OH) 2 + 2 H + → Ba 2+ + 2 H 2 O. The same equation relating the concentrations of acid and base applies. The concept of neutralization is not limited to reactions in solution. For example, the reaction of limestone with acid such as sulfuric acid is also a neutralization ...

  4. 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 ...

  5. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    The relative rates at which different halogens react vary considerably: [citation needed] fluorine (108) > chlorine (1) > bromine (7 × 10 −11) > iodine (2 × 10 −22).. Radical fluorination with the pure element is difficult to control and highly exothermic; care must be taken to prevent an explosion or a runaway reaction.

  6. Electrophilic halogenation - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_halogenation

    Halogenation of benzene where X is the halogen, catalyst represents the catalyst (if needed) and HX represents the protonated base. A few types of aromatic compounds, such as phenol , will react without a catalyst , but for typical benzene derivatives with less reactive substrates, a Lewis acid is required as a catalyst .

  7. Halous acid - Wikipedia

    en.wikipedia.org/wiki/Halous_acid

    A halous acid, also known as a halogenous acid, [1] is an oxyacid consisting of a halogen atom in the +3 oxidation state single-bonded to a hydroxyl group and double-bonded to an oxygen atom. Examples include chlorous acid, bromous acid, and iodous acid. The conjugate base is a halite.

  8. Metal halides - Wikipedia

    en.wikipedia.org/wiki/Metal_halides

    The halogens can all react with metals to form metal halides according to the following equation: 2M + nX 2 → 2MX n. where M is the metal, X is the halogen, and MX n is the metal halide. Sample of silver chloride. In practice, this type of reaction may be very exothermic, hence impractical as a preparative technique.

  9. Hydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrohalogenation

    A hydrohalogenation reaction is the electrophilic addition of hydrogen halides like hydrogen chloride or hydrogen bromide to alkenes to yield the corresponding haloalkanes. [ 1 ] [ 2 ] [ 3 ] If the two carbon atoms at the double bond are linked to a different number of hydrogen atoms, the halogen is found preferentially at the carbon with fewer ...