Lipids from 78.2 grams of seal blubber were extracted with 100 mL of diethyl ether. The solution was dried and the lipids emulsified in 75 mL of aqueous solution that contained 66.7 μmoles of polar bear pancreatic lipase and 33.3 μmoles monoacylglycerol lipase. The emulsion was stirred at 25 °C for 15 hours, after which the lipids were extracted with 75 mL of carbon tetrachloride. Draw the chemical structure of the solute that is expected to be most prevalent in the aqueous phase.
The lipid extracted with diethyl ether (lipid is water insoluble)
the solution is dried and lipids are emulsified in 75mL of aqueous solution with 66.7 μmoles of polar bear pancreatic lipase and 33.3 μmoles monoacylglycerol lipase.
So this combination will hydrolyze the lipid as
lipid + 2 H2O
glycerol + fatty acid anions
The left over lipid was extracted with CCl4.
So in the aqueous phas there will be
monoacylglcyerol and fatty acid
Lipids from 78.2 grams of seal blubber were extracted with 100 mL of diethyl ether. The...
What is the purpose of extracting the aqueous layer two more
times with ether in step 5?
What is the purpose of washing the combined organic layers with
NaOH in step 6?
Thank you
Reaction 1: Nitration HNO3 NO2 + H2SO4, H20 NO2 toluene NO2 ortho meta para Procedure for Reaction 1: 1) To a stirred solution of 3 ml (44.7 mmoles) 67 % HNO3 in 3.75 mL of water, H2SO4 (9 mL) was slowly added at 10-15 °C. 2)...
using the procedure above complete the stoichiometry
table
Procedure In an oven-dried, 100 ml round bottom flask containing magnetic stirring bar was added hydrobenzoin (1.0 8.4.7 mmol), anhydrous iron(III) chloride (0.3 g, 1.8 mmol), and anhydrous acetone (30 ml). The mixture was heated to reflux and stirred for 30 min. The reaction mixture was cooled tort and transferred to a separatory funnel containing 10% aq potassium carbonate (10 mL). Water (50 mL) was added and the aqueous solution was extracted...