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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. Electron configuration - Wikipedia

    en.wikipedia.org/wiki/Electron_configuration

    The molecular orbitals are labelled according to their symmetry, [e] rather than the atomic orbital labels used for atoms and monatomic ions; hence, the electron configuration of the dioxygen molecule, O 2, is written 1σ g 2 1σ u 2 2σ g 2 2σ u 2 3σ g 2 1π u 4 1π g 2, [39] [40] or equivalently 1σ g 2 1σ u 2 2σ g 2 2σ u 2 1π u 4 3σ g ...

  5. Hydrogen disulfide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_disulfide

    The structure of hydrogen disulfide is similar to that of hydrogen peroxide, with C 2 point group symmetry. Both molecules are distinctly nonplanar. The dihedral angle between the H a −S−S and S−S−H b planes is 90.6°, compared with 111.5° in H 2 O 2. The H−S−S bond angle is 92°, close to 90° for unhybridized divalent sulfur. [1]

  6. Solvated electron - Wikipedia

    en.wikipedia.org/wiki/Solvated_electron

    2 [Na(NH 3) 6] + e − → H 2 + 2 NaNH 2 + 10 NH 3. Electride salts can be isolated by the addition of macrocyclic ligands such as crown ether and cryptands to solutions containing solvated electrons. These ligands strongly bind the cations and prevent their re-reduction by the electron. [Na(NH 3) 6] + e − + cryptand → [Na(cryptand)] + e ...

  7. 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 ...

  8. Sulfurous acid - Wikipedia

    en.wikipedia.org/wiki/Sulfurous_acid

    Sulfuric(IV) acid (United Kingdom spelling: sulphuric(IV) acid), also known as sulfurous (UK: sulphurous) acid and thionic acid, [citation needed] is the chemical compound with the formula H 2 SO 3. Raman spectra of solutions of sulfur dioxide in water show only signals due to the SO 2 molecule and the bisulfite ion, HSO − 3. [2]

  9. Cyanate - Wikipedia

    en.wikipedia.org/wiki/Cyanate

    Sodium cyanate is isostructural with sodium fulminate, confirming the linear structure of the cyanate ion. [3] It is made industrially by heating a mixture of sodium carbonate and urea. [4] Na 2 CO 3 + 2 OC(NH 2) 22 NaNCO + CO 2 + 2 NH 3 + H 2 O. A similar reaction is used to make potassium cyanate. Cyanates are produced when cyanides are ...