Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Provide mechanism with curved arrows for
Part C: Synthesis of tetraphenylcyclopentadienone

Transcribed Image Text:Experiment 9C: Aldol Condensation (Data Sheet)
Running the reaction
0.44 g of dibenzyl ketone and 0.43 g of benzil were dissolved in 3 mL of absolute ethanol
in a 10 mL round-bottom flask
After adding a spin bar and an air condenser, the mixture was heated to a gentle reflux
0.50 mL of ethanolic potassium hydroxide was added dropwise
The color changed immediately from bright yellow to dark brown
During the 10 min of reflux, a very dark precipitate formed
Product isolation
The mixture was allowed to cool down to room temperature before being placed in an ice-
bath
The solids were isolated by vacuum filtration using a Hirsch funnel
The solids were washed with 1 mL of ice-cold 95 % ethanol being air was sucked through
the crystals for 10 minutes (=crude)
The crude was recrystallized from 15 mL of 95 % ethanol: toluene (1:1)
The hot, saturated solution was allowed to cool down slowly using a hot water bath
After 30 minutes, the mixture cooled to room temperature and was placed in an ice-bath
The crystals were isolated by vacuum filtration using a Hirsch funnel
The crystals were air-dried before characterization
TLC data: mobile phase: hexane: ethyl acetate (3:1), stationary phase: SiO2, dibenzyl
ketone: 11 mm, benzil: 35 mm, product: 71 mm (only one spot in the lane), solvent front:
88 mm
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