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  2. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    The benzyl cation or phenylcarbenium ion is the carbocation with formula C 6 H 5 CH + 2; the benzyl anion or phenylmethanide ion is the carbanion with the formula C 6 H 5 CH − 2. None of these species can be formed in significant amounts in the solution phase under normal conditions, but they are useful referents for discussion of reaction ...

  3. Benzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Benzyl_alcohol

    Benzyl alcohol (also known as α-cresol) is an aromatic alcohol with the formula C 6 H 5 CH 2 OH. The benzyl group is often abbreviated "Bn" (not to be confused with "Bz" which is used for benzoyl), thus benzyl alcohol is denoted as BnOH. Benzyl alcohol is a colorless liquid with a mild pleasant aromatic odor.

  4. Cresol - Wikipedia

    en.wikipedia.org/wiki/Cresol

    The Occupational Safety and Health Administration has set a permissible exposure limit at 5 ppm (22 mg/m 3) over an eight-hour time-weighted average, while the National Institute for Occupational Safety and Health recommends a limit of 2.3 ppm (10 mg/m 3).

  5. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Benzyl chloride is prepared industrially by the gas-phase photochemical reaction of toluene with chlorine: [3] C 6 H 5 CH 3 + Cl 2 → C 6 H 5 CH 2 Cl + HCl. In this way, approximately 100,000 tonnes are produced annually. The reaction proceeds by the free radical process, involving the intermediacy of free chlorine atoms. [4]

  6. Chloroformate - Wikipedia

    en.wikipedia.org/wiki/Chloroformate

    Typically these reactions would be conducted in the presence of a base which serves to absorb the HCl. Alkyl chloroformate esters degrate to give the alkyl chloride, with retention of configuration: ROC(O)Cl ' → RCl + CO 2. The reaction is proposed to proceed via a substitution nucleophilic internal mechanism. [3]

  7. p-Chlorocresol - Wikipedia

    en.wikipedia.org/wiki/P-Chlorocresol

    p-Chlorocresol, or 4-chloro-3-methylphenol (ClC 6 H 3 CH 3 OH), also known as p-chloro-m-cresol, is a potent disinfectant and antiseptic. [1] It appears as a pinkish white crystalline solid. [ 2 ] It is also used as a preservative [ 3 ] in cosmetics and medicinal products for both humans and animals.

  8. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    or normal amyl alcohol primary Pentan-1-ol: 138.5 2-methyl-1-butanol or active amyl alcohol primary 2-Methylbutan-1-ol: 128.7 3-methyl-1-butanol or isoamyl alcohol or isopentyl alcohol primary 3-Methylbutan-1-ol: 131.2 2,2-dimethyl-1-propanol or neopentyl alcohol primary 2,2-Dimethylpropan-1-ol: 113.1 2-pentanol or sec-amyl alcohol or methyl (n ...

  9. p-Cresol - Wikipedia

    en.wikipedia.org/wiki/P-cresol

    ch 3 c 6 h 4 so 3 h + 2 naoh → ch 3 c 6 h 4 oh + na 2 so 3 + h 2 o Other methods for the production of p -cresol include chlorination of toluene followed by hydrolysis. In the cymene-cresol process, toluene is alkylated with propene to give p -cymene , which can be oxidatively dealkylated in a manner similar to the cumene process .