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  2. Phases of fluorine - Wikipedia

    en.wikipedia.org/wiki/Phases_of_fluorine

    Henri Moissan's 1892 record of fluorine gas color, viewed end-on in a 5‑m tube. Air (1) is on the left, fluorine (2) is in the middle, chlorine (3) is on the right. Fluorine forms diatomic molecules (F 2) that are gaseous at room temperature with a density about 1.3 times that of air.

  3. Fluorine - Wikipedia

    en.wikipedia.org/wiki/Fluorine

    Fluorine is a chemical element; it has symbol F and atomic number 9. It is the lightest halogen [ note 1 ] and exists at standard conditions as pale yellow diatomic gas. Fluorine is extremely reactive as it reacts with all other elements except for the light inert gases .

  4. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    The covalent radius of fluorine of about 71 picometers found in F 2 molecules is significantly larger than that in other compounds because of this weak bonding between the two fluorine atoms. [9] This is a result of the relatively large electron and internuclear repulsions, combined with a relatively small overlap of bonding orbitals arising ...

  5. Color of chemicals - Wikipedia

    en.wikipedia.org/wiki/Color_of_chemicals

    The color of chemicals is a physical property of chemicals that in most cases comes from the excitation of electrons due to an absorption of energy performed by the chemical. The study of chemical structure by means of energy absorption and release is generally referred to as spectroscopy .

  6. Hydrogen fluoride - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_fluoride

    Hydrogen fluoride does not boil until 20 °C in contrast to the heavier hydrogen halides, which boil between −85 °C (−120 °F) and −35 °C (−30 °F). [ 6 ] [ 7 ] [ 8 ] This hydrogen bonding between HF molecules gives rise to high viscosity in the liquid phase and lower than expected pressure in the gas phase.

  7. Fluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Fluorocarbon

    Perfluoroalkanes are very stable because of the strength of the carbon–fluorine bond, one of the strongest in organic chemistry. [4] Its strength is a result of the electronegativity of fluorine imparting partial ionic character through partial charges on the carbon and fluorine atoms, which shorten and strengthen the bond (compared to carbon-hydrogen bonds) through favorable covalent ...

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  9. Flame test - Wikipedia

    en.wikipedia.org/wiki/Flame_test

    A flame test involves introducing a sample of the element or compound to a hot, non-luminous flame and observing the color of the flame that results. [4] The compound can be made into a paste with concentrated hydrochloric acid, as metal halides, being volatile, give better results. [5] Different flames can be tried to verify the accuracy of ...