Assignment Lab Notebook of Module 07
Assignment Lab Notebook of Module 07
Assignment Lab Notebook of Module 07
#07
AIM: A mixture of benzoic acid and 1,2-diphenyl ethandione in dichloromethane will be separated by a
liquid-liquid extraction.
Note: having any of these solutions of HCl and NaOH enter the eye will be painful and may constitute a health risk. Safety
glasses MUST be worn at all times.
Consult the Master Table of Reagents and only add reagents and chemicals needed for this experiment to complete this table. The
Master Table of Reagents is given as a link in the Main Table of Module 07.
Note: The above table has more entries than required. Also for the chemical HCl, both concentrated and dilute solutions of HCl
can simply be added as one entry of the chemical HCl reported in Master Table of Reagents. Same applies for NaOH.
1
Pictorial Flow Chart: In the pictorial flow chart provided on the left hand side of the page, fill in the correct compound in the
boxes provided with the letters B for benzoic acid, C for benzoate anion (the conjugate base of benzoic acid) and D for 1,2-diphenyl
ethandione. Note that each box may contain more than one of these compounds B, C or D, or none at all.
Before shaking
NaOH aq.
CH2Cl2
After shaking
beaker # 2
NaOH aq.
CH2Cl2
Write down the acid base reaction that occurs
in sections 1 and 2 (if no reaction occurs, write NO RXN):
flask # 1
2
Procedure: Section 3 OBSERVATIONS :
Before shaking
water
CH2Cl2
flask # 1
After shaking
water
Collect organic
layer into flask #3
flask # 3
3
Procedure : Section 4: Draw your own flow chart OBSERVATIONS :
for sections 4.
4
Procedure Section 5 : Draw your own flow chart for section 5. OBSERVATIONS :
5
Procedure Section 6: Draw your own flow chart OBSERVATIONS :
for sections 6.
6
Procedure Section 7: Draw your own flow chart
OBSERVATIONS :
for sections 7.
7
RESULTS:
Note: The benzoic acid and diketone obtained in this experiment will be stored in your mini-locker to dry.
The following results (i.e. mass recovery and m.pt.) will be measured the following week using your dried
samples. Also, for online students, no penalty is given for wrong descriptions of crystals.
[Show your calculations below] Refer to Appendix F for an example on how to calculate % mass recovery.
Reminder: Temp 1 is when the crystals start to melt and Temp 2 is the temperature at which all the sample has
completely melted. The word “slow” indicates that the increases to temperature must be slow so that you do not
overshoot the temperature range at which melting of your known solid occurs. Note: No fast rate determination was
needed.
8
Mass of recrystallized 1,2 diphenyl ethandione:
crystals:____________________________________________________
[Show your calculations below] Remember that the maximum recovery possible is 0.50 grams.
crystals:____________________________________________________
9
CONCLUSION:
Remember that the conclusion must always be related to the aim of the experiment, in this case “the separation of a mixture using
liquid-liquid extraction”. For example, you can comment on your mass recovery results and where you may have lost compound, you
can comment on the relationship between melting point range and purity of your benzoic acid sample; you can also comment on the
reasons why the experiment was able to separate the mixture, give facts to support your conclusion.
10