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  2. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    [1] [2] [3] Introduced by Gilbert N. Lewis in his 1916 article The Atom and the Molecule, a Lewis structure can be drawn for any covalently bonded molecule, as well as coordination compounds. [4] Lewis structures extend the concept of the electron dot diagram by adding lines between atoms to represent shared pairs in a chemical bond.

  3. Sulfamic acid - Wikipedia

    en.wikipedia.org/wiki/Sulfamic_acid

    Ball-and-stick model of a sulfamic acid zwitterion as it occurs in the crystal state. [4]The compound is well described by the formula H 3 NSO 3, not the tautomer H 2 NSO 2 (OH). The relevant bond distances are 1.44 Å for the S=O and 1.77 Å for the S–N.

  4. Oxidation state - Wikipedia

    en.wikipedia.org/wiki/Oxidation_state

    3.3.1 Applied to a Lewis structure. 3.3.2 Applied to bond graph. 3.4 Balancing redox. ... Again, this is an average value since the structure of the molecule is H 3 C ...

  5. Tetrahedral molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_molecular_geometry

    In a tetrahedral molecular geometry, a central atom is located at the center with four substituents that are located at the corners of a tetrahedron.The bond angles are arccos(− ⁠ 1 / 3 ⁠) = 109.4712206...° ≈ 109.5° when all four substituents are the same, as in methane (CH 4) [1] [2] as well as its heavier analogues.

  6. Linnett double-quartet theory - Wikipedia

    en.wikipedia.org/wiki/Linnett_Double-Quartet_Theory

    The cornerstone of classical bonding theories is the Lewis structure, published by G. N. Lewis in 1916 and continuing to be widely taught and disseminated to this day. [3] In this theory, the electrons in bonds are believed to pair up, forming electron pairs which result in the binding of nuclei .

  7. Hyponitrite - Wikipedia

    en.wikipedia.org/wiki/Hyponitrite

    In organic chemistry, it may also refer to the group −O−N=N−O−, or any organic compound with the generic formula R 1 −O−N=N−O−R 2, where R 1 and R 2 are organic groups. [1] Such compounds can be viewed as salts and esters of hyponitrous acid. An acid hyponitrite is an ionic compound with the anion HN 2 O − 2 ([HON=NO] −).

  8. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    For example, the double-bond carbons in alkenes like C 2 H 4 are AX 3 E 0, but the bond angles are not all exactly 120°. Likewise, SOCl 2 is AX 3 E 1, but because the X substituents are not identical, the X–A–X angles are not all equal. Based on the steric number and distribution of Xs and Es, VSEPR theory makes the predictions in the ...

  9. Hydrogen isocyanide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_isocyanide

    Hydrogen isocyanide (HNC) is a linear triatomic molecule with C ∞v point group symmetry.It is a zwitterion and an isomer of hydrogen cyanide (HCN). [2] Both HNC and HCN have large, similar dipole moments, with μ HNC = 3.05 Debye and μ HCN = 2.98 Debye respectively. [3]