updated last Wednesday, August 20, 2014


Week 7 Problem Set 30 BL (Esterification Reaction)


Useful Link: Refractometer

ATTN: answers to the below questions are due at the start of your lab period; these answers should be part of your pre-lab write-up.


Administrative Issues

1. Please consult your TA directly in order to find out when a particular postlab report is due. The red reader outlines the tentative schedule which has to be adjusted from time to time depending on how the section proceeds with the in-lab work.

2. If you have questions of general nature, please post them on the course discussion board instead of sending it to the instructor. Answering the same question several times is not productive for anybody.

3. The report for the project will be due by Tuesday, September 2, 2014 at 12:00 pm (in paper) and on the same day by 10 pm (on www.turnitin.com, CourseID: 8107579, Password: Chem30BL).

1. Please watch the following video (MP4-format), review the TLC chapter in the reader and the TLC lecture module (PP and lecture), take the online quiz read the appropriate chapter in the "Survival Kit Reader".

Video: Thin Layer Chromatography

Quiz: (http://bacher.chem.ucla.edu/TakeQuiz/?id=d3d9446802a44259755d38e6d163e820). The quiz is worth 10 points, and has to be taken until one hour prior to the in-lab meeting 7. (Hint: In some cases more than one answer is correct!) Even though you can take the quiz until one hour prior to meeting 7 of your section, you should not delay taking it since there might be some problems with the server. There seem to be problems with some MAC systems as well. After you submit the answers, your score should appear on your screen. If this does not happen, you will have to retake the quiz. (There will not be any possibility to retake the quiz weeks later!). In order to take the quiz, you have to go through a UCLA ICP address. This means that you either have to use your Bruin-Online account or go through the VPN (Vitual Private Network, software can be found here: http://www.bol.ucla.edu/services/vpn/) to have this UCLA ICP address. To log in, use your last name and your student ID. If you are experiencing problems, contact the instructor via email and include your full name (indicated which one is your last name), your student ID and section .

2. Reaction planning of esterification carried out in the lab

a. Which compound is used in excess in this reaction? Why is this approach necessary?

b. What is used as catalyst in the reaction. Show the appropriate key intermediate assuming the student uses malonic acid for the reaction.

c. After the completion of the reaction, the mixture is chilled. After the addition of water, the student observes the formation of a small amount of oil. No precipitate is observed at this point either. Rationalize this observation.

d. The student adds diethyl ether to the mixture obtained in c.. He does not observe a phase separation. Explain. How should he proceed?

e. After finally getting a phase separation, he combines the organic layers and extracts them with saturated sodium bicarbonate solution. How does the student know that he is done with this step? Show pertinent balanced chemical equations.

f. The crude ester is distilled in vacuo. The student observes that some of his liquid collects in the Hickman head while some of it remains in the conical vial. Rationalize this observation. How should the student proceed?

3. A student refluxes a mixture of 4.15 g of phthalic acid, 5.00 mL of methanol and 0.50 mL of concentrated sulfuric acid for three hours. After the work-up, the student isolated 3.64 g of the product.

a. Show a balanced chemical equation for the reaction.

b. Determine the percentage yield of the reaction. Show all calculations.

c. Predict the boiling point of the product at p = 40 torr.

d. The student observes refractive index of nD24= 1.5050. Which conclusion can he draw from this observation?

e. How many signals does the product exhibit in the 1H-NMR and the 13C-NMR, respectively? How do these signals look like? In which range do they fall?

f. What is the most important use of the product in this reaction?