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  2. 4-Chlorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Chlorobenzaldehyde

    clc 5 h 4 chcl 2 + h 2 o → clc 5 h 4 cho + 2 hcl It can also be produced by the oxidation of 4-chlorobenzyl alcohol . [ 3 ] [ 4 ] It can be further oxidized to 4-chlorobenzoic acid . [ 5 ]

  3. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Indicative of its high reactivity (relative to alkyl chlorides), benzyl chloride slowly reacts with water in a hydrolysis reaction to form benzyl alcohol and hydrochloric acid. In contact with mucous membranes, hydrolysis produces hydrochloric acid. Thus, benzyl chloride is a lachrymator and has been used in chemical warfare. It is also very ...

  4. Benzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Benzyl_alcohol

    Benzyl alcohol is a colorless liquid with a mild pleasant aromatic odor. It is useful as a solvent for its polarity, low toxicity, and low vapor pressure. Benzyl alcohol has moderate solubility in water (4 g/100 mL) and is miscible in alcohols and diethyl ether.

  5. 4-Chlorobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/4-Chlorobenzoic_acid

    4-Chlorobenzoic acid is an organic compound with the molecular formula ClC 6 H 4 CO 2 H. It is a white solid that is soluble in some organic solvents and in aqueous base. 4-Chlorobenzoic acid is prepared by oxidation of 4-chlorotoluene .

  6. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

  7. Benzyl cyanide - Wikipedia

    en.wikipedia.org/wiki/Benzyl_cyanide

    Benzyl cyanide is used as a solvent [14] and as a starting material in the synthesis of fungicides (e.g. Fenapanil), [15] fragrances (phenethyl alcohol), antibiotics, [2] and other pharmaceuticals. The partial hydrolysis of BnCN results in 2-phenylacetamide .

  8. Benzyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloroformate

    Benzyl chloroformate is commonly used in organic synthesis for the introduction of the benzyloxycarbonyl (formerly called carboxybenzyl) protecting group for amines.The protecting group is abbreviated Cbz or Z (in honor of discoverer Zervas), hence the alternative shorthand designation for benzyl chloroformate as Cbz-Cl or Z-Cl.

  9. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.