Examples of 'ml of diethyl ether' in a sentence
Meaning of "ml of diethyl ether"
ml of diethyl ether: This phrase specifies a measurement unit for volume, where 'ml' stands for milliliters, and 'diethyl ether' is a chemical compound. It indicates a quantity of diethyl ether substance often used in laboratory experiments, research, or industrial processes
How to use "ml of diethyl ether" in a sentence
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ml of diethyl ether
One hundred mL of diethyl ether is added and then filtered.
It is then washed with 5 mL of diethyl ether.
Thereto were added 50 ml of diethyl ether and the deposited precipitate was isolated by filtration.
The solution obtained is extracted with 5 ml of diethyl ether.
Addition of 20 ml of diethyl ether produces a red precipitate which is separated off by filtration.
Then the suspension was diluted with 3 ml of diethyl ether and filtrated.
Approximately 70 ml of diethyl ether was added to reaction, resulting in precipitate formation.
The remaining mixture was stirred vigorously and 50 mL of diethyl ether was added.
To the remaining solution 40 ml of diethyl ether was slowly added resulting in a white precipitate.
The product is precipitated from the obtained solution with 50 ml of diethyl ether.
This lipid film was dissolved in 1 ml of diethyl ether washed with distilled water.
After cooling with ice the reaction mixture is treated with 10 ml of diethyl ether.
When the mixture was diluted with 10 ml of diethyl ether more product precipitated.
The condensate is transferred to a separatory funnel and extracted twice with 30 mL of diethyl ether.
The residue was then dissolved in 30 mL of diethyl ether and triturated with hexanes.
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The separated aqueous phase was separated and washed with an additional 30 ml of diethyl ether.
Approximately 70 mL of diethyl ether was added to reaction.
The solvent is then evaporated and the residue triturated with twice 20 ml of diethyl ether.
The mixture was evaporated, 2 ml of diethyl ether was added and stirred.
The resulting cloudy mixture was filtered through celite and washed with 30 ml of diethyl ether.
The residue was dissolved in 20 ml of diethyl ether and filtered.
Furthermore, 30 ml of diethyl ether was added and stirred, whereby crystals were precipitated.
The blended material was then slowly added to 10 ml of diethyl ether while stirring.
An additional 100 mL of diethyl ether is added and the mixture filtered.
Remove the lead acetate paper and add 1 to 2 ml of diethyl ether and shake gently.
Then 150 ml of diethyl ether was added to dissolve the product of the reaction.
The yellow solution thus obtained is cooled and then diluted with 50 ml of diethyl ether.
It is diluted with 100 ml of diethyl ether and left to stand overnight.
The product obtained is solubilised in CH 3 OH and poured over 3 ml of diethyl ether.
After the addition of 500 ml of diethyl ether a clean phase separation was obtained.
G of cyclohexanecarboxylic acid chloride are dissolved in 50 ml of diethyl ether.
The mixture is poured into 500 ml of diethyl ether and the precipitate collected.
The reaction medium is precipitated from 20 ml of diethyl ether.
An additional 15 mL of diethyl ether is added and the solution stirred vigorously for 1 hour.
To this solution was slowly added 20 ml of diethyl ether.
An additional 100 mL of diethyl ether is added and then filtered.
G of the free base was dissolved in 40 ml of diethyl ether.
Thereafter, 20 ml of diethyl ether was added, and stirring was continued for 10 more minutes.
The solvent is concentrated and 50 ml of diethyl ether are added.
Then, 20 ml of diethyl ether was added thereto, and the precipitate was filtered off.
The metabolites are extracted twice with 60 ml of diethyl ether.
After the addition of a further 120 ml of diethyl ether the product precipitates completely.
The product was precipitated by the addition of 20 ml of diethyl ether.
A precipitate formed when about 400 mL of diethyl ether was added to the DMF-enriched solution.
To the reaction mixture was then added 50 mL of diethyl ether.
To the residue, 220 ml of diethyl ether were added, followed by distillation under reduced pressure.
The residue was suspended in 20 mL of diethyl ether.
After the addition of 100 ml of diethyl ether and decanting, the solution is evaporated.
The aqueous layer was extracted with 50 mL of diethyl ether.
The resulting slurry was added to 250 ml of diethyl ether and the solids filtered.
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