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  2. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  3. Benzonitrile - Wikipedia

    en.wikipedia.org/wiki/Benzonitrile

    Benzonitrile is a useful solvent and a versatile precursor to many derivatives. It reacts with amines to afford N-substituted benzamides after hydrolysis. [3] It is a precursor to diphenylmethanimine via reaction with phenylmagnesium bromide followed by methanolysis.

  4. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75

  5. Acetophenone - Wikipedia

    en.wikipedia.org/wiki/Acetophenone

    In instructional laboratories, [5] acetophenone is converted to styrene in a two-step process that illustrates the reduction of carbonyls using sodium borohydride and the dehydration of alcohols: 4 C 6 H 5 C(O)CH 3 + NaBH 4 + 4 H 2 O → 4 C 6 H 5 CH(OH)CH 3 + NaOH + B(OH) 3 C 6 H 5 CH(OH)CH 3 → C 6 H 5 CH=CH 2 + H 2 O

  6. tert-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/Tert-Butylbenzene

    tert-Butylbenzene can be produced by the treatment of benzene with isobutene [1] or by the reaction of benzene with tert-butyl chloride in presence of anhydrous aluminium chloride, [2] the latter is depicted below:

  7. Benzilic acid rearrangement - Wikipedia

    en.wikipedia.org/wiki/Benzilic_acid_rearrangement

    The benzilic acid rearrangement is formally the 1,2-rearrangement of 1,2-diketones to form α-hydroxy–carboxylic acids using a base.This reaction receives its name from the reaction of benzil with potassium hydroxide to form benzilic acid.

  8. Cannizzaro reaction - Wikipedia

    en.wikipedia.org/wiki/Cannizzaro_reaction

    2 C 6 H 5 CHO + KOH → C 6 H 5 CH 2 OH + C 6 H 5 COOK. The process is a redox reaction involving transfer of a hydride from one substrate molecule to the other: one aldehyde is oxidized to form the acid, the other is reduced to form the alcohol. [3]

  9. Hexamethylbenzene - Wikipedia

    en.wikipedia.org/wiki/Hexamethylbenzene

    Hexamethylbenzene, also known as mellitene, is a hydrocarbon with the molecular formula C 12 H 18 and the condensed structural formula C 6 (CH 3) 6.It is an aromatic compound and a derivative of benzene, where benzene's six hydrogen atoms have each been replaced by a methyl group.