enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 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.

  3. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    Benzyl bromide is an isomer, which has a bromine substituted for one of the hydrogens of toluene's methyl group, and it is sometimes named α-bromotoluene.

  4. 3-Quinuclidinyl benzilate - Wikipedia

    en.wikipedia.org/wiki/3-Quinuclidinyl_benzilate

    As a powerful anticholinergic agent, BZ produces a syndrome of effects known as the anticholinergic toxidrome: these include both psychological and physiological effects, with the most incapacitating effect being a state of delirium characterized by cognitive dysfunction, hallucinations, and inability to perform basic tasks.

  5. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    Benzyl group and derivatives: Benzyl group, benzyl radical, benzyl amine, benzyl bromide, benzyl chloroformate, and benzyl methyl ether. R = heteroatom, alkyl, aryl, allyl etc. or other substituents. In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5.

  6. Category:Benzyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Benzyl_compounds

    This page was last edited on 6 September 2024, at 07:50 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  7. Category:Lachrymatory agents - Wikipedia

    en.wikipedia.org/wiki/Category:Lachrymatory_agents

    Help; Learn to edit; Community portal; Recent changes; Upload file; Special pages

  8. Benzoyl group - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_group

    The benzoyl functional group.. In organic chemistry, benzoyl (/ ˈ b ɛ n z oʊ ɪ l /, BENZ-oh-il) [1] is the functional group with the formula −COC 6 H 5 and structure −C(=O)−C 6 H 5. [2] [3] It can be viewed as benzaldehyde missing one hydrogen.

  9. Baker–Nathan effect - Wikipedia

    en.wikipedia.org/wiki/Baker–Nathan_effect

    [2] [3] [4] They examined the chemical kinetics for the reaction of pyridine with benzyl bromide to form a pyridinium salt, and a series of benzyl bromides having different alkyl groups as substituents at the para position.