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  2. Bromoform - Wikipedia

    en.wikipedia.org/wiki/Bromoform

    Bromoform was discovered in 1832 by Löwig who distilled a mixture of bromal and potassium hydroxide, as analogous to preparation of chloroform from chloral. [5]Bromoform can be prepared by the haloform reaction using acetone and sodium hypobromite, by the electrolysis of potassium bromide in ethanol, or by treating chloroform with aluminium bromide.

  3. Phenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylboronic_acid

    Phenylboronic acid or benzeneboronic acid, abbreviated as PhB(OH) 2 where Ph is the phenyl group C 6 H 5 - and B(OH) 2 is a boronic acid containing a phenyl substituent and two hydroxyl groups attached to boron. Phenylboronic acid is a white powder and is commonly used in organic synthesis.

  4. Fluoroalcohol - Wikipedia

    en.wikipedia.org/wiki/Fluoroalcohol

    Most primary and secondary perfluoroalcohols are unstable, for example trifluoromethanol eliminates hydrogen fluoride, forming carbonyl fluoride. [2] This reaction is reversible. [3] CF 3 OH → COF 2 + HF. Stable perfluorinated alcohols include nonafluoro-tert-butyl alcohol ((CF 3) 3 COH) and pentafluorophenol (C 6 F 5 OH).

  5. Fluorobenzene - Wikipedia

    en.wikipedia.org/wiki/Fluorobenzene

    PhN=N-N(CH 2) 5 + 2 HF → PhF + N 2 + [(CH 2) 5 NH 2]F. Historical note: in Wallach's era, the element fluorine was symbolized with "Fl". Thus, his procedure is subtitled "Fluorbenzol, C 6 H 5 Fl". [1] On the laboratory scale, PhF is prepared by the thermal decomposition of the benzenediazonium tetrafluoroborate: PhN 2 BF 4 → PhF + BF 3 + N 2

  6. You Can Use Vinegar and Baking Soda To Remove Rust - AOL

    www.aol.com/lifestyle/vinegar-baking-soda-remove...

    Just aim for a solution that's saturated with salt. Step 2: Submerge the Rusty Object Place the rusty object in the container, ensuring that it's completely submerged in the vinegar-and-salt solution.

  7. Benzyl bromide - Wikipedia

    en.wikipedia.org/wiki/Benzyl_bromide

    Benzyl bromide is an organic compound with the formula C 6 H 5 CH 2 Br. The molecule consists of a benzene ring substituted with a bromomethyl group. It is a colorless liquid with lachrymatory properties. The compound is a reagent for introducing benzyl groups. [3] [4]

  8. 1-Bromo-4-fluorobenzene - Wikipedia

    en.wikipedia.org/wiki/1-Bromo-4-fluorobenzene

    4-Fluorobromobenzene is synthesized via bromination of fluorobenzene in the presence of a Lewis acid catalyst such as iron(III) bromide or aluminium tribromide. [2]4-Bromofluorobenzene is regarded by the Toxic Substances Control Act as a high production volume chemical, that is, a chemical that 1 million pounds (about 500 tonnes) per year is either produced in or imported to the United States.

  9. Dibromomethane - Wikipedia

    en.wikipedia.org/wiki/Dibromomethane

    The bromochloromethane product from either reaction can further react in a similar manner: 6 CH 2 BrCl + 3 Br 2 + 2 Al → 6 CH 2 Br 2 + 2 AlCl 3 CH 2 BrCl + HBr → CH 2 Br 2 + HCl. In the laboratory, it is prepared from bromoform using sodium arsenite and sodium hydroxide: [4] CHBr 3 + Na 3 AsO 3 + NaOH → CH 2 Br 2 + Na 3 AsO 4 + NaBr

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