Examples of 'ml of benzene' in a sentence
Meaning of "ml of benzene"
ml of benzene - Milliliter (ml) of benzene is a unit of measurement used to quantify the volume of benzene, a chemical compound commonly used in various industrial processes, laboratories, and applications. This phrase is employed in scientific contexts when dealing with specific amounts of benzene
How to use "ml of benzene" in a sentence
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ml of benzene
After evaporation the residue was dissolved in a few ml of benzene and Left overnight.
A microcrystalline solid was so obtained which was dissolved in 6 ml of benzene.
The reaction mixture is kept refluxing in 10 ml of benzene under an atmosphere of nitrogen.
The aqueous layer was further subjected to two times of extraction with 8 ml of benzene.
The remaining residue was extracted with 45 ml of benzene to give a clear yellow filtrate.
The sodium chloride is separated by filtration and washed with two times 5 ml of benzene.
The resulting residue was mixed with 10 ml of benzene and again concentrated under a reduced pressure.
It is filtered and then washed with 5 ml of benzene.
The residue is dissolved in 10 ml of benzene and precipitated with cyclohexane.
Thereafter the salts are filtered off and the filtrate is diluted with 50 ml of benzene.
The residue is dissolved in 30 ml of benzene and refluxed for 1 hour.
It is concentrated under vacuum, adding three times 20 ml of benzene.
G of paratoluenesulfonic acid and 300 ml of benzene are put into a reaction vessel.
The mixture was extracted three times with 80 ml of benzene.
The solid was diluted with 500 ml of benzene and product was dissolved.
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The aqueous fractions were again extracted twice with 10 ml of benzene.
The solution was extracted with 350 ml of benzene as described in the paper.
After separation, the aqueous layer was extracted with an additional 50 ml of benzene.
A solution of the obtained azide in 50 ml of benzene is refluxed for 1 hour.
The triethylamine chlorohydrate is filtered and washed twice with 200 ml of benzene.
To the residue is added 200 ml of benzene to make the crystals to finely particulate.
The residue was stirred with 40 mL of benzene.
The solution is diluted with 200 ml of benzene and left to rise to room temperature.
The salts are filtered and discarded, the filtrate is diluted with 40 ml of benzene.
The residue was mixed with 100 ml of benzene and the resulting crystals were filtered off.
The finely divided precipitate was collected on a filter and redissolved in 400 ml of benzene.
Therefore, the reaction mixture was treated with 0.5 ml of benzene and shaken for a few seconds.
After refluxing 24 h and subsequent cooling, the reaction mixture was extracted with 10 mL of benzene.
The solution is then diluted with 50 mL of benzene and washed with brine and 1N HCl.
The rose-colored precipitate formed is separated and washed twice with 100 ml of benzene each time.
The residue is taken up in 50 ml of benzene and 10 g of alumina are added.
Moles of 6 bromohexanoyl chloride are dissolved in 150 ml of benzene.
The residue is dissolved in 15 ml of benzene and extracted with 15 ml of water.
The residue was then dissolved in 500 ml of benzene.
G of plant extract is shaken with 10 ml of benzene and filtered.
The phases are separated, the aqueous layer is extracted with 2 x 100 ml of benzene.
The reaction medium is cooled, diluted with 90 ml of benzene and filtered.
Mg of the cyclic compound 6 produced in Example 1 was dissolved in 10 ml of benzene.
To the solution was added 2.2 g of thiophosgene in 10 ml of benzene dropwise with stirring.
After removing the solvent, the residue was dissolved into 100 ml of benzene.
To the residue was added 50 ml of benzene.
The reaction mixture is taken up with 100 ml of benzene.
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Your doctor will prescribe the dose in ml
Six to eight ml of hydrogen peroxide will be necessary
