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Cyclohexane [110-82-71 M 84.2, f 6.6O, b 80.7O, d24 0.77410, n 1.42623, n25 1.42354.
    Commonly, washed with conc H2SO4 until the washings are colourless, followed by water, aq Na2C03 or 5%
NaOH, and again water until neutral. It is next dried with P2O5, Linde type 4A molecular sieves, CaC12, or
MgS04 then Na and distd. Cyclohexane has been refluxed with, and distd from Na, CaH2, LiAl& (which also
removes peroxides), sodiudpotassium alloy, or P2O5. Traces of *benzene can be removed by passage through
a column of silica gel that has been freshly heated: this gives material suitable for ultraviolet and infrared
spectroscopy. If there is much *benzene in the cyclohexane, most of it can be removed by a preliminary
treatment with nitrating acid (a cold mixture of 3OmL conc HNO3 and 70mL of conc H2SO4) which converts
*benzene into nitrobenzene.
The impure cyclohexane and the nitrating acid are placed in an ice bath and stirred
vigorously for 15min, after which the mixture is allowed to warm to 25O during lh. The cyclohexane is
decanted, washed several times with 25% NaOH, then water dried with CaC12, and distd from sodium.
Carbonyl-containing impurities can be removed as described for chloroform. Other purification procedures
include passage through columns of activated alumina and repeated crystn by partial freezing. Small quantities
may be purified by chromatography on a Dowex 710-Chromosorb W gas-liquid chromatographic column.
Rapid purification: Distil, discarding the forerun. Stand distillate over Grade I alumina (5% w/v) or 4A
molecular sieves.

[ Last edited by jianmei97 on 2007-6-13 at 12:24 ]
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