LOYOLA COLLEGE (AUTONOMOUS), CHENNAI – 600 034
B.Sc. DEGREE EXAMINATION – CHEMISTRY
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FOURTH SEMESTER – APRIL 2008
CH 4500 – ORGANIC CHEMISTRY – II
Date : 26/04/2008 Dept. No. Max. : 100 Marks
Time : 9:00 – 12:00
Part-A
Answer ALL questions. (10 ´ 2 = 20)
- ‘cyclopropane is more reactive than cyclohexane’. Why?
- What are the conformers possible for cyclohexane? Which one is more stable? Why?
- How would you distinguish methanol from ethanol by means of chemical tests?
- ‘Williamson’s synthesis is useful for the preparation of both simple and mixed ethers’. Justify this statement with suitable examples.
- Arrange the following in the increasing order of their acidity. Justify your answer.
Monochloroacetic acid, Dichloroacetic acid, Acetic acid, Formic acid and Trichloro acetic acid.
- What happens when maleic acid is treated with bromine? Identify the stereochemistry of the product obtained?
- Name the electrophile in nitration of benzene. What are the evidences for its existence?
- ‘Aniline does not undergo Friedel-Craft’s reaction’. Why?
- How would you prepare the following from benzene diazonium chloride?
(i) Benzene and (ii) Benzoic acid - Give the mechanism of Reimer-Tiemann reaction.
Part-B
Answer any EIGHT questions. (8 ´ 5 = 40)
- Explain Baeyer’s strain theory in the stability of cycloalkanes.
- How are alcohols prepared from hydroboration-oxidation method? Explain with mechanism.
- An amide(A) having molecular formula C3H7ON on hydrolysis gives an acid C3H6O2(B). (B) on chlorination in the presence of red phosphorus produces a chloroacid(C).The latter on boiling with aqueous NaOH and subsequent acidification forms lactic acid(D).Write the reactions and identify the structure of A, B, C and D.
- What happens when benzaldehyde is heated with alcoholic KCN solution? Explain the mechanism.
- How would you prepare 4-methylpentanoic and 3-methylbutanoic acid using diethyl malonate?
- Explain the mechanism of Hofmann-bromamide reaction. Name the intermediate in this reaction.
- ‘Nitration of benzene is irreversible while sulphonation of benzene is a reversible reaction.’ Explain.
- What are sulpha drugs? Explain the mechanism of action of sulpha durgs.
- What happens when 3-bromo-2, 3-dimethyl pentane is treated with alcoholic KOH? Identify the different products obtained and explain with mechanism.
- Explain the mechanism of Baeyer-Villiger rearrangement.
- Explain the synthetic utility of acetoacetic ester with examples.
- Explain aromaticity, antiaromaticity and nonaromaticity with suitable examples.
Part-C
Answer any FOUR questions. (4 ´ 10 = 40)
- a) Explain the mechanism of reduction of CH3COOC2H5 by LiAlH4.
- b) Compare the stereochemistry of products obtained in Sn1 and Sn2 reactions.
- a) How are grignard reagents used in the preparation of primary, secondary and tertiary alcohols? Explain with suitable examples.
- b) Explain the mechanism of preparation of ethers by oxymercuration- demercuration method.
- a) How are the following compounds prepared?
(i) acrylic acid (ii) cinnamic acid (iii) maleic acid - b) Explain the action of heat on a-, b- and g-hydroxy acids and identify the products obtained.
- a) Explain the mechanism of sulphonation of benzene
- b) ‘Halogens are deactivating groups but o-, p- directing’.
- a) How will you synthesise the following compounds from benzaldehyde?
(i) Mandelic acid (ii) m-Benzaldehydesulphonic acid
- b) Write a note on: (a) Cannizaro reaction (b) Perkin reaction
- a) Explain Claisen and abnormal Claisen rearrangements with mechanism.
- b) How would you convert m-nitrophenol from nitrobenzene? Explain all the steps involved in this process.