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  2. 2-Phenylhexane - Wikipedia

    en.wikipedia.org/wiki/2-Phenylhexane

    2-Phenylhexane is an aromatic hydrocarbon. It can be produced by a Friedel-Crafts alkylation between 1-chlorohexane and benzene ., [ 1 ] or by the reaction of benzene and 1-hexene with various acid catalysts such as antimony pentafluoride , [ 2 ] scandium(III) triflate , [ 3 ] and phosphoric acid .

  3. 1-Chlorohexane - Wikipedia

    en.wikipedia.org/wiki/1-chlorohexane

    The chemical formula is CH 3 (CH 2) 5 Cl. [2] [3] Synthesis. ... 2-Phenylhexane can be prepared by reacting the compound with benzene and aluminum trichloride. [5]

  4. List of chlorinated propanes - Wikipedia

    en.wikipedia.org/wiki/List_of_chlorinated_propanes

    1,1,1,2,3,3,3-Heptachloropropane; Octachloro. Octachloropropane; References This page was last edited on 23 January 2023, at 01:25 (UTC). Text is available under the ...

  5. C3-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C3-Benzenes

    The C 3-benzenes are a class of organic aromatic compounds which contain a benzene ring and three other carbon atoms. For the hydrocarbons with no further unsaturation, there are four isomers. The chemical formula for all the saturated isomers is C 9 H 12 .

  6. Hypochlorous acid is a natural molecule in the body but can also be used in skincare. Experts share how it’s used and why it’s the latest buzzy ingredient.

  7. These Batch Cosmos Are Made to Serve a Crowd - AOL

    www.aol.com/batch-cosmos-made-serve-crowd...

    3 oz. triple sec or other orange liqueur. 1. orange, for garnish. Directions. Combine the vodka, cranberry juice, lime juice, and triple sec in a pitcher filled with ice. Stir well until chilled ...

  8. Why food safety experts stand behind the 'when in doubt ... - AOL

    www.aol.com/why-food-safety-experts-stand...

    December 5, 2024 at 2:00 AM. With the inflated price of groceries today, people might be wondering how much they can kick the can when it comes to the expiration dates of an array of items.

  9. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    H 2 C=CH 2 + HCl → CH 3 CH 2 Cl. In oxychlorination, hydrogen chloride instead of the more expensive chlorine is used for the same purpose: CH 2 =CH 2 + 2 HCl + 1 ⁄ 2 O 2 → ClCH 2 CH 2 Cl + H 2 O. Secondary and tertiary alcohols react with hydrogen chloride to give the corresponding chlorides.