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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

    Sulfamic acid melts at 205 °C before decomposing at higher temperatures to water, sulfur trioxide, sulfur dioxide and nitrogen. [2] Sulfamic acid (H 3 NSO 3) may be considered an intermediate compound between sulfuric acid (H 2 SO 4), and sulfamide (H 4 N 2 SO 2), effectively replacing a hydroxyl (–OH) group with an amine (–NH 2) group at

  4. Peroxynitrite - Wikipedia

    en.wikipedia.org/wiki/Peroxynitrite

    Peroxynitrite can be prepared by the reaction of superoxide with nitric oxide: [1] [2] [3] NO + O − 2 → NO(O 2) −. It is prepared by the reaction of hydrogen peroxide with nitrite: [4] H 2 O 2 + NO − 2 → ONOO − + H 2 O. Its presence is indicated by the absorbance at 302 nm (pH 12, ε 302 = 1670 M −1 cm −1).

  5. Reactive oxygen species - Wikipedia

    en.wikipedia.org/wiki/Reactive_oxygen_species

    F: hydrogen peroxide (H 2 O 2); G: nitric oxide (NO •) In chemistry and biology, reactive oxygen species (ROS) are highly reactive chemicals formed from diatomic oxygen (O 2), water, and hydrogen peroxide. Some prominent ROS are hydroperoxide (O 2 H), superoxide (O 2 −), [1] hydroxyl radical (OH.), and singlet oxygen. [2]

  6. Tris - Wikipedia

    en.wikipedia.org/wiki/Tris

    As temperature rises from 25 °C to 37 °C, the pH of a tris buffer will decrease an average of 0.025 units per degree. [ 9 ] In general, a 10-fold increase in tris buffer concentration will lead to a 0.05 unit increase in pH and vice versa.

  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. Thiol - Wikipedia

    en.wikipedia.org/wiki/Thiol

    The S−H bond is much weaker than the O−H bond as reflected in their respective bond dissociation energies (BDE). For CH 3 S−H, the BDE is 366 kJ/mol (87 kcal/mol), while for CH 3 O−H, the BDE is 440 kJ/mol (110 kcal/mol). [10] An S−H bond is moderately polar because of the small difference in the electronegativity of sulfur and ...

  9. Nitrous acid - Wikipedia

    en.wikipedia.org/wiki/Nitrous_acid

    Nitrous acid (molecular formula H N O 2) is a weak and monoprotic acid known only in solution, in the gas phase, and in the form of nitrite (NO − 2) salts. [3] It was discovered by Carl Wilhelm Scheele, who called it "phlogisticated acid of niter".