Loyola College M.Sc. Chemistry April 2008 Photochemistry & Organic Synthesis Question Paper PDF Download

GH 38

 

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)

  1. How hydroxyl groups are added on to carbon-carbon multiple bonds?
  2. Draw the Frontier Molecular Orbital picture for the cycloaddition of 1,3-butadiene and ethylene.
  3. Predict the product.
  4. Give an example for 3,3-sigmatropic rearrangement and explain the mechanism.
  5. State Stark Einstein and Grothus Draper laws of photochemistry.
  6. What is Norrish type II reaction? Give an example.
  7. How protective groups are important in the synthesis of an organic compound?
  8. What are synthons? Identify suitable synthetic equivalents for the following synthons.

C6H5CH2+, (CH3)2CH¯

  1. Write the mechanism of SeO2 oxidation.
  2. Why convergent synthesis is a better technique than stepwise synthesis?

 

Part – B

Answer any EIGHT questions.                                                          (8 ´ 5 = 40 marks)

  1. Explain the mechanism of NaBH4 reductions with an example.
  2. How regioselectivity is explained in cycloaddition reactions? Give suitable examples.
  3. The following compound undergoes sigmatropic rearrangement reaction. Write the mechanism of the reaction and predict the product/s.

 

  1. Predict the stereochemistry of the product and write the mechanism of the reaction.

 

  1. Explain the Barton reaction in steroidal compounds.
  2. How photoisomerisation takes place in alkene compounds? Explain with any two examples.
  3. Write the retrosynthesis of the following compounds.
  4. How are monofunctionalised compounds prepared from alkylhalides? Write a scheme to explain this.
  5. What is electroorganic synthesis? Elaborate on electrooxidation reactions with suitable examples.
  6. Discuss on C-C disconnections in 1,3- and 1,4-difunctionalised compounds with examples.
  7. Write a short note on aldol and crossed aldol condensation reactions.
  8. Bring out the differences between Clemmensen and Wolff Kishner reductions with suitable example.

Part – C

Answer any FOUR questions.                                                           (4 ´ 10 = 40 marks)

  1. Write the mechanism of the following reactions and explain.
  2. a) Knoevenagel reaction
  3. b) Claisen-Schmidt reaction
  4. c) Darzen’s reaction
  5. How are the following compounds synthesized by retrosynthetic approach?

 

  1. a) Write the photochemical rearrangement of 4,4-diphenylcyclohex-2-en-1-one with complete mechanism.
  2. b) Explain various photochemical processes taking place in the excited state.
  3. a) Explain the mechanism of Paterno Buchii reaction in alkenes.
  4. b) Find out the products with proper stereochemistry in the following reactions.
  5. Explain the mechanism of the following reactions.

 

 

  1. a) Write the complete mechanism of synthesis of cubane.
  2. b) Explain the chemoselectivity of the oxidizing agents with suitable examples.

 

 

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