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  2. Tetralin - Wikipedia

    en.wikipedia.org/wiki/Tetralin

    Tetralin (1,2,3,4-tetrahydronaphthalene) is a hydrocarbon having the chemical formula C 10 H 12. It is a partially hydrogenated derivative of naphthalene . It is a colorless liquid that is used as a hydrogen-donor solvent .

  3. 2,2',3,3',4,4'-Hexachlorobiphenyl - Wikipedia

    en.wikipedia.org/wiki/2,2',3,3',4,4...

    The IUPAC name of 2,2',3,3',4,4'-hexachlorobiphenyl is 1,2,3-trichloro-4-(2,3,4-trichlorophenyl) benzene and its molecular formula is C 12 H 4 Cl 6. It is a light yellow, soft, sticky resin and has a boiling point of 385-420 °C. Its flash point lies around 141 °C and its melting point around 150 °C. [1]

  4. Defining equation (physical chemistry) - Wikipedia

    en.wikipedia.org/wiki/Defining_equation...

    Theoretical chemistry requires quantities from core physics, such as time, volume, temperature, and pressure.But the highly quantitative nature of physical chemistry, in a more specialized way than core physics, uses molar amounts of substance rather than simply counting numbers; this leads to the specialized definitions in this article.

  5. 1,2,3,4-Butanetetracarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/1,2,3,4-Butanetetra...

    1,2,3,4-Butanetetracarboxylic acid is an organic compound with the formula HO 2 CCH 2 CH(CO 2 H)CH(CO 2 H)CH 2 CO 2 H. It is one of the simplest stable tetracarboxylic acids. The compound exists as two diastereomers, meso and the (R,R)/(S,S) pair. All are white solids. The compound is produced by oxidation of tetrahydrophthalic anhydride. [1]

  6. 1,2,3,4-Tetraphenylnaphthalene - Wikipedia

    en.wikipedia.org/wiki/1,2,3,4-Tetraphenylnaphthalene

    1,2,3,4-Tetraphenylnaphthalene is a polycyclic aromatic hydrocarbon commonly prepared in the undergraduate teaching laboratory as an introduction to the Diels-Alder reaction, in this case between benzyne, which acts as the dienophile, (generated in situ) and tetraphenylcyclopentadienone, which acts as the diene. [3]

  7. Sandpaper - Wikipedia

    en.wikipedia.org/wiki/Sandpaper

    The first recorded instance of sandpaper was in 13th-century China when crushed shells, seeds, and sand were bonded to parchment using natural gum. [2] [3] Shark skin (placoid scales) has also been used as an abrasive, and the rough scales of the Coelacanth are used for the same purpose by the natives of Comoros. [4]

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    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. p-Xylene - Wikipedia

    en.wikipedia.org/wiki/P-Xylene

    The p-stands for para-, indicating that the two methyl groups in p-xylene occupy the diametrically opposite substituent positions 1 and 4. It is in the positions of the two methyl groups, their arene substitution pattern, that it differs from the other isomers, o-xylene and m-xylene. All have the same chemical formula C 6 H 4 (CH 3) 2. All ...