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  2. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    A simple Lewis model also does not account for the phenomenon of aromaticity. For instance, Lewis structures do not offer an explanation for why cyclic C 6 H 6 (benzene) experiences special stabilization beyond normal delocalization effects, while C 4 H 4 (cyclobutadiene) actually experiences a special destabilization.

  3. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    Examples of Lewis bases based on the general definition of electron pair donor include: simple anions, such as H − and F −; other lone-pair-containing species, such as H 2 O, NH 3, HO −, and CH 3 −; complex anions, such as sulfate; electron-rich π-system Lewis bases, such as ethyne, ethene, and benzene

  4. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    For example, many chemical compounds exist in different isomeric forms, which have different enantiomeric structures but the same molecular formula. There are multiple types of ways to draw these structural formulas such as: Lewis structures , condensed formulas, skeletal formulas , Newman projections , Cyclohexane conformations , Haworth ...

  5. Chemical bonding of water - Wikipedia

    en.wikipedia.org/wiki/Chemical_bonding_of_water

    Lewis Structure of H 2 O indicating bond angle and bond length. Water (H 2 O) is a simple triatomic bent molecule with C 2v molecular symmetry and bond angle of 104.5° between the central oxygen atom and the hydrogen atoms.

  6. Chemical bond - Wikipedia

    en.wikipedia.org/wiki/Chemical_bond

    Examples of Lewis dot diagrams used to represent electrons in the chemical bonds between atoms, here showing carbon (C), hydrogen (H), and oxygen (O). Lewis diagrams were developed in 1916 by Gilbert N. Lewis to describe chemical bonding and are still widely used today. Each line segment or pair of dots represents a pair of electrons.

  7. Single bond - Wikipedia

    en.wikipedia.org/wiki/Single_bond

    The structure of pi bonds does not allow for rotation (at least not at 298 K), so the double bond and the triple bond which contain pi bonds are held due to this property. The sigma bond is not so restrictive, and the single bond is able to rotate using the sigma bond as the axis of rotation (Moore, Stanitski, and Jurs 396-397).

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  9. Radical (chemistry) - Wikipedia

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

    The hydroxyl radical, Lewis structure shown, contains one unpaired electron. Lewis dot structure of a Hydroxide ion compared to a hydroxyl radical. In chemistry, a radical, also known as a free radical, is an atom, molecule, or ion that has at least one unpaired valence electron.