|
LOYOLA COLLEGE (AUTONOMOUS), CHENNAI – 600 034
M.Sc. DEGREE EXAMINATION – CHEMISTRY
THIRD SEMESTER – APRIL 2008
CH 3808 – PHOTOCHEMISTRY AND ORGANIC SYNTHESIS
Date : 26-04-08 Dept. No. Max. : 100 Marks
Time : 9:00 – 12:00
Part – A
Answer ALL questions. (10 ´ 2 = 20 marks)
- How hydroxyl groups are added on to carbon-carbon multiple bonds?
- Draw the Frontier Molecular Orbital picture for the cycloaddition of 1,3-butadiene and ethylene.
- Predict the product.
- Give an example for 3,3-sigmatropic rearrangement and explain the mechanism.
- State Stark Einstein and Grothus Draper laws of photochemistry.
- What is Norrish type II reaction? Give an example.
- How protective groups are important in the synthesis of an organic compound?
- What are synthons? Identify suitable synthetic equivalents for the following synthons.
C6H5CH2+, (CH3)2CH¯
- Write the mechanism of SeO2 oxidation.
- Why convergent synthesis is a better technique than stepwise synthesis?
Part – B
Answer any EIGHT questions. (8 ´ 5 = 40 marks)
- Explain the mechanism of NaBH4 reductions with an example.
- How regioselectivity is explained in cycloaddition reactions? Give suitable examples.
- The following compound undergoes sigmatropic rearrangement reaction. Write the mechanism of the reaction and predict the product/s.
- Predict the stereochemistry of the product and write the mechanism of the reaction.
- Explain the Barton reaction in steroidal compounds.
- How photoisomerisation takes place in alkene compounds? Explain with any two examples.
- Write the retrosynthesis of the following compounds.
- How are monofunctionalised compounds prepared from alkylhalides? Write a scheme to explain this.
- What is electroorganic synthesis? Elaborate on electrooxidation reactions with suitable examples.
- Discuss on C-C disconnections in 1,3- and 1,4-difunctionalised compounds with examples.
- Write a short note on aldol and crossed aldol condensation reactions.
- Bring out the differences between Clemmensen and Wolff Kishner reductions with suitable example.
Part – C
Answer any FOUR questions. (4 ´ 10 = 40 marks)
- Write the mechanism of the following reactions and explain.
- a) Knoevenagel reaction
- b) Claisen-Schmidt reaction
- c) Darzen’s reaction
- How are the following compounds synthesized by retrosynthetic approach?
- a) Write the photochemical rearrangement of 4,4-diphenylcyclohex-2-en-1-one with complete mechanism.
- b) Explain various photochemical processes taking place in the excited state.
- a) Explain the mechanism of Paterno Buchii reaction in alkenes.
- b) Find out the products with proper stereochemistry in the following reactions.
- Explain the mechanism of the following reactions.
- a) Write the complete mechanism of synthesis of cubane.
- b) Explain the chemoselectivity of the oxidizing agents with suitable examples.
Latest Govt Job & Exam Updates: