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BSc Sem V 2015 2016 2016 Chemistry 2 Question Paper - Mumbai University | munotes

TyBsc Sem V Chemistry 2 2015.pdf
SEM V · 2015-2016 · 1 May 2025

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Questions asked in this paper

  • (2) Figures to the right indicate full marks
  1. Q1 Answer any three of the following 5 marks
    • (A) What is Pinacol-pinacolone rearrangement? Give an example and
    • (B) (a) What are kinetically controlled reactions? Explain with any two 3
    • (b) State and explain Hofmann rule of elimination. 2
    • (C) (a) Write the products formed in the following reactions ethereaction 3
    • (b) Explain nucleophilicity with example
    • (D) (a) Give the mechanism the following reaction. 3
    • (b) Explain the of Beckmann rearrangement with a suitable 2
    • (E) (a) What is E1 reagtion? Discuss its mechanism
    • (b) Complete reactions 2
    • (a) Give the mechanism involved in the acid catalysed esterification 3
    • (b) What is Benzilic acid rearrangement? Give an example. 2
  2. Q2 Answer any three of the following Calculate angle
    • (A) Explain the concept of ‘angle strain'in their planar cyclopropane, cyclobutane and cyclop entane, structures. ism and
    • (B) Complete the following reaction. Explain its
    • C) Draw two chair conformations each of cis and trans 5 diethylcyclohexane. Which of the four conformers 1S stable? Why?
    • (D) Explain mechanism and stereochemistry of brominat trans-2-butene 5
    • (E) of chirality of spirans with
    • (F) Explain mechanism and stereochemistry of bagginduced dehydro genation 5 of 1-bromo-1,2-dipheny! propane. Why called anti-elimination
  3. Q3 Answer any three of the following S
    • (A) (a) What are monosaccharides? the importance of amphiprotic solvent in the mechanism of mut tion
    • (b) Write the open chain for the following ring structures
    • (B) () Write a note on Kiliani-Fische ) (a) What are epimers and 2
    • (b) How will you convert D(+) a ive 3
    • (D) (a) Assuming configuration of D (+) glucose derive the configuration of 3
    • (b) Complete the following reactions. 2 &
    • (E) (a) Explain : glucose is a reducing sugar whereas sucrose is reducing 3 sugar. What is the action of HIO, on glucose?
    • (b) Write the stepwise reactions of excess of phenyl on glucose
    • (F) (a) Write the structures of the following
    • (i) 1,3- oxazole
    • (b) Give the IUPAC names of : 2 4, Answer any three of the followidy
    • (A) (a) Explain Hofmaga exhaustive methylation & elimination reaction with 3
    • (b) Write synthesis for preparation of pyrrole. 2
    • (b) resonance structures of furan. 2
    • (C) (a will you convert?
    • (ii) to thiophene
    • (iii) to Tetrabromopyrrole
    • (b) Discuss the aromaticity of pyridine
    • (D) Explain 'multicomponent synthesis' with any two examples. 5
    • (E) Write synthesis of the following:- 5s
    • (a) Indigo from anthranilic acid
    • (b) Green synthesis
    • (F) Explain the use of microwaves in organic synthesis with any two examples
  4. Q5 (A) Choose the right answer from the alternatives given below and rewrite the completed
    • (b) Saytzeff elimination of alkyl halide forms olefin as the
    • (c) Sulphonation of naphthalene at given a mixture of
    • (d) In the alkaline hydrolysis of an ester, the end are
    • (A) State whether the following are true or false 4
    • (p) Basicity is a kinetic pro
    • (q) preferably from the syn-periplanar } Anions have than neutral molecules
    • (s) 1s a self- condensation of esters without
    • (B) Fill in the blanks
    • (b) In reactions, a levorotatory substrate no In catalytic hydrogenation, a cis substrate ct
    • (B) State whether the following molecules are chiral or achiral. 4
    • (C) Write the structures of the following compounds. 4
    • (a) 1-bromo-1,2 -pentadiene S
    • (b) 6-bromospiro [3, 5] nonane
    • (d) 3-methylbicyclo [4,2,0] octane
    • (C) Give the IU PAC names of the following 4
    • (D) Complete the following reactions:
    • (D) Match the columns appropriately :- >

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