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  2. Phenolphthalein - Wikipedia

    en.wikipedia.org/wiki/Phenolphthalein

    Phenolphthalein is slightly soluble in water and usually is dissolved in alcohols in experiments. It is a weak acid, which can lose H + ions in solution. The nonionized phenolphthalein molecule is colorless and the double deprotonated phenolphthalein ion is fuchsia. Further proton loss in higher pH occurs slowly and leads to a colorless form.

  3. List of states of matter - Wikipedia

    en.wikipedia.org/wiki/List_of_states_of_matter

    Strange matter: A type of quark matter that may exist inside some neutron stars close to the Tolman–Oppenheimer–Volkoff limit (approximately 2–3 solar masses). May be stable at lower energy states once formed. Quark matter: Hypothetical phases of matter whose degrees of freedom include quarks and gluons Color-glass condensate

  4. Phthalein dye - Wikipedia

    en.wikipedia.org/wiki/Phthalein_dye

    Chemical structure of phenolphthalein, a common phthalein dye. Phthalein dyes are a class of dyes mainly used as pH indicators, due to their ability to change colors depending on pH. [1] They are formed by the reaction of phthalic anhydride with various phenols. They are a subclass of triarylmethane dyes. Common phthalein dyes include ...

  5. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    Deprotonation of a phenol forms a corresponding negative phenolate ion or phenoxide ion, and the corresponding salts are called phenolates or phenoxides (aryloxides according to the IUPAC Gold Book). [ citation needed ]

  6. Base (chemistry) - Wikipedia

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

    Concentrated or strong bases are caustic on organic matter and react violently with acidic substances. Aqueous solutions or molten bases dissociate in ions and conduct electricity. Reactions with indicators: bases turn red litmus paper blue, phenolphthalein pink, keep bromothymol blue in its natural colour of blue, and turn methyl orange-yellow.

  7. Phenol red - Wikipedia

    en.wikipedia.org/wiki/Phenol_red

    At still higher pH (pK a = 7.7), the phenol's hydroxy group loses its proton, resulting in the red ion denoted as PS 2−. [6] In several sources, the structure of phenol red is shown with the sulfur atom being part of a cyclic group, similar to the structure of phenolphthalein.

  8. Kastle–Meyer test - Wikipedia

    en.wikipedia.org/wiki/Kastle–Meyer_test

    Upon reduction, the very intense pink color of the cationic form of phenolphthalein fades to a faint yellow color. It is this form of phenolphthalein that is present in Kastle–Meyer test kits. In order to generate the intense pink color indicative of a positive test, the reduced phenolphthalein must be oxidized back to its normal, colored form.

  9. Atomic, molecular, and optical physics - Wikipedia

    en.wikipedia.org/wiki/Atomic,_molecular,_and...

    Atomic, molecular, and optical physics (AMO) is the study of mattermatter and light–matter interactions, at the scale of one or a few atoms [1] and energy scales around several electron volts. [2]: 1356 [3] The three areas are closely interrelated. AMO theory includes classical, semi-classical and quantum treatments.