Organic Chemistry II Laboratory manual Assignment

Organic Chemistry II Laboratory manual  Assignment Words: 848

Page 1 of 8 Expect. L . Catenation of a-C)-gloriousness Procedure: 1 . Preheat solution of Zincs in a ml pear shape flask with air condenser (0. 5 g anhydrous Zincs in 12. 5 ml acetic anhydride, this will be provided by lab. Technician) in water bath for 10-15 minis. 2. Add slowly 2. 5 g (0. 014 mol) of powdered C)-glucose in small portions (roughly in 7-10 3. Swirl the mixture gently during the addition to control the vigorous reaction and keep swirling to dissolve the powder added.. 4. 5. After addition is completed, heat the flask on a water bath for one hour.

Cool the intent of the flask with cold water, and then pour into ice water (120 ml) and stir vigorously to assist the hydrolysis of unrelated acetic anhydride. 6. 7. 8. 9. After 30 min, the oil which first separates will gradually solidify. * Collect the crude product using Hirsch funnel. Record the melting point. Dissolve the crude product in minimal amount of hot methanol. Once the crude product is dissolved, let it cool down and pour water to recitalist it. 10. Filter out the rationalized product. 11. Record the melting point. (the literature value is 1. In this experiment,a a-C)-gloriousness is obtained.

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If we use co) Question (Mice)20/McCann to react with powdered C)-glucose, -D-gloriousness will be resulted. Explain. -??END-?? Page 2 of 8 Expect. 2. CICS-l anhydride (Dills-alder reaction) The Dills-Alder reaction is an important, synthetically useful reaction in organic chemistry. It is named after Otto Dills and his student Kurt Alder who were awarded the Nobel Prize in chemistry in 1950 in recognition of the importance of their discovery. The Dills-Alder reaction is the syllabication of a 1 ,3-TO system (a dine) with a bond that usually bears an electrocardiographs group (a downhill) to reduce a six-member ring.

The reaction is concerted (bond breaking and forming occur simultaneously) and therefore results in high stereotypically (products with predictable stereotypical). Butadiene as the dine and malefic anhydride as the downhill. These substrates react to form the Dills-Alder product, CICS-??l OZ,6-tetrahedron-4,5-demographically anhydride. After synthesizing your anhydride, you will need to purify it by rationalizations, and characterize it by obtaining a melting point and an IR spectrum Page 3 of 8 Procedure 1 . Weigh 0. 72 g (0. 74 mol) of finely powdered malefic anhydride contained in a small conical flask. Add 0. 65 g (0. 0080 mol) of freshly distilled 2,3-timetabled-1 ,3-dine (this will be provided by lab. Technician) to (addition should be performed in fume cupboard). Wrap the conical flask and tilt the flask to ensure malefic anhydride is immersed into the dine solution. Reaction occurs in a few minutes (indicated by evolution of heat). Allow to stand until the mixture attains room temperature. Add -?? ml acetone to dissolve the mixture. Add -?? ml water to precipitate out the product.

Wash with ml water for two times. Wash with ml petroleum ether (b. P. 60-80 co) for two times. 10. Air dry the product upon filter paper. 1 1 . Record the yield and its melting point. (the literature value is co) 12. Obtain an IR spectrum of your product and identify the characteristic signals of the compound. Question 1 . Is the adduct of the reaction in end or ex. form? Explain. 2. If some of the product the acid in the product? Page 4 of 8 Expect. 3. Photochemical Reaction and Acid-catcalled Rearrangement: Preparation of Pensacola and Opinionatedly Procedures: Part A: 1 .

Dissolve phenomenon (3 g) with ‘so-propane (20 ml) in a 50-ml Erlenmeyer flask by warming on the stream bath. Add more ‘so-propane (-??10 ml) and acetic acid (half drop) to the flask; transfer the solution to a given-test tube; wash the Erlenmeyer flask with ‘so-propane and transfer to fill up the test tube, stopper the test tube with a well-rolled tight fitting cork ensuring there is no air bubble trapped in the tube. Expose the solution to direct IV light for 1 week to complete the reaction (hand in your reaction mixture to our Lab Technician for this IV activated reaction).

Since noncompliance is sparingly soluble in ‘so-propane, it will crystallize out once is formed. Part a: 1 . Chill the flask and collect the crystals by a Hirsch funnel. 2. Dry the crystals and record the yield together with its m. P. (the literature value 3. Add Pensacola (1 g) (from part A), acetic acid (5 ml) and one small crystal of iodine ((about 0. 01 g) too pear-shaped flask fitted with a condenser. (In case your yield is less than 1 g, please add in the other reagent in correct proportion. Reflux the solution for 1-2 minutes until the crystals dissolve and reflux for further 5 ins.

Cool the solution, the pinochle separate as paste; filter the paste and wash it free from iodine by 95% ethanol (about 1-2 ml). Recitalist the crystals from a suitable solvent (made a suggestion and consult your demonstrator; hint: like dissolve like and record the amount of solvent used in your report) Record the yield and m. P. Of the crystals. (the literature value is 1 . Write the feasible mechanism for the formation of Pensacola and Opinionatedly -?? END-?? Page 5 of 8 Expect. 4. Michael Addition: Preparation of 1-Phenyl-3-phenylaminopyrrolidine-2, 5-iodine. Part A Preparation of Millennial acid (A) 1 .

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