enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Expressing resonance when drawing Lewis structures may be done either by drawing each of the possible resonance forms and placing double-headed arrows between them or by using dashed lines to represent the partial bonds (although the latter is a good representation of the resonance hybrid which is not, formally speaking, a Lewis structure).

  3. Trimethylborane - Wikipedia

    en.wikipedia.org/wiki/Trimethylborane

    Trimethylborane is a strong Lewis acid. B(CH 3) 3 can form an adduct with ammonia: (NH 3):B(CH 3) 3. [13] as well as other Lewis bases. The Lewis acid properties of B(CH 3) 3 have been analyzed by the ECW model yielding E A = 2.90 and C A = 3.60.

  4. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    Lewis structure is best used to calculate formal charges or how atoms bond to each other as both electrons and bonds are shown. Lewis structures give an idea of the molecular and electronic geometry which varies based on the presence of bonds and lone pairs and through this one could determine the bond angles and hybridization as well.

  5. Methenium - Wikipedia

    en.wikipedia.org/wiki/Methenium

    In organic chemistry, methenium (also called methylium, carbenium, [2] methyl cation, or protonated methylene) is a cation with the formula CH + 3.It can be viewed as a methylene radical (: CH

  6. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    The most common Lewis bases are anions. The strength of Lewis basicity correlates with the pK a of the parent acid: acids with high pK a 's give good Lewis bases. As usual, a weaker acid has a stronger conjugate base. Examples of Lewis bases based on the general definition of electron pair donor include: simple anions, such as H − and F −

  7. Borane - Wikipedia

    en.wikipedia.org/wiki/Borane

    Molecular species BH 3 is a very strong Lewis acid. It can be isolated in the form of various adducts, such as borane carbonyl, BH 3 (CO). [11] Molecular BH 3 is believed to be a reaction intermediate in the pyrolysis of diborane to produce higher boranes: [5] B 2 H 6 ⇌ 2BH 3 BH 3 +B 2 H 6 → B 3 H 7 +H 2 (rate determining step) BH 3 + B 3 H ...

  8. Trigonal prismatic molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Trigonal_prismatic...

    In chemistry, the trigonal prismatic molecular geometry describes the shape of compounds where six atoms, groups of atoms, or ligands are arranged around a central atom, defining the vertices of a triangular prism. The structure commonly occurs for d 0, d 1 and d 2 transition metal complexes with covalently-bound ligands and small charge ...

  9. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    [1]: 416 The geometry of the central atoms and their non-bonding electron pairs in turn determine the geometry of the larger whole molecule. The number of electron pairs in the valence shell of a central atom is determined after drawing the Lewis structure of the molecule, and expanding it to show all bonding groups and lone pairs of electrons.