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  2. Potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_permanganate

    4 KMnO 4 + 4 KOH → 4 K 2 MnO 4 + O 2 + 2 H 2 O. This reaction illustrates the relatively rare role of hydroxide as a reducing agent. Addition of concentrated sulfuric acid to potassium permanganate gives Mn 2 O 7. [76] Although no reaction may be apparent, the vapor over the mixture will ignite paper impregnated with alcohol.

  3. Ethylbenzene - Wikipedia

    en.wikipedia.org/wiki/Ethylbenzene

    Ethylbenzene is an organic compound with the formula C 6 H 5 CH 2 CH 3. It is a highly flammable, colorless liquid with an odor similar to that of gasoline . This monocyclic aromatic hydrocarbon is important in the petrochemical industry as a reaction intermediate in the production of styrene , the precursor to polystyrene , a common plastic ...

  4. BTX (chemistry) - Wikipedia

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

    If ethylbenzene is included, the mixture is sometimes referred to as BTEX. The BTX aromatics are very important petrochemical materials. Global consumption of benzene, estimated at more than 40,000,000 tons in 2010, showed an unprecedented growth of more than 3,000,000 tons from the level seen in 2009.

  5. Potassium manganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_manganate

    2 MnO 2 + 4 KOH + O 2 → 2 K 2 MnO 4 + 2 H 2 O. The transformation gives a green-colored melt. Alternatively, instead of using air, potassium nitrate can be used as the oxidizer: 2 KOH + KNO 3 + MnO 2 → K 2 MnO 4 + H 2 O + KNO 2. One can test an unknown substance for the presence of manganese by heating the sample in strong KOH in air.

  6. Acetophenone - Wikipedia

    en.wikipedia.org/wiki/Acetophenone

    Acetophenone is also generated from ethylbenzene hydroperoxide. Ethylbenzene hydroperoxide is primarily converted to 1-phenylethanol (α-methylbenzyl alcohol) in the process with a small amount of by-product acetophenone. Acetophenone is recovered or hydrogenated to 1-phenylethanol which is then dehydrated to produce styrene.

  7. Cannizzaro reaction - Wikipedia

    en.wikipedia.org/wiki/Cannizzaro_reaction

    2 C 6 H 5 CHO + KOH → C 6 H 5 CH 2 OH + C 6 H 5 COOK. The process is a redox reaction involving transfer of a hydride from one substrate molecule to the other: one aldehyde is oxidized to form the acid, the other is reduced to form the alcohol. [3]

  8. Transalkylation - Wikipedia

    en.wikipedia.org/wiki/Transalkylation

    In organic chemistry, transalkylation is a chemical reaction involving the transfer of an alkyl group from one organic compound to another. The reaction is used for the transfer of methyl and ethyl groups between benzene rings.

  9. Ethyl group - Wikipedia

    en.wikipedia.org/wiki/Ethyl_group

    Ethyl group (highlighted blue) as part of a molecule, as the ethyl radical, and in the compounds ethanol, bromoethane, ethyl acetate, and ethyl methyl ether.. In organic chemistry, an ethyl group (abbr. Et) is an alkyl substituent with the formula −CH 2 CH 3, derived from ethane (C 2 H 6).