Course: M.Sc.
Specialization: ORGANIC CHEMISTRY
                          Practical Syllabus (Semester: III; Batch: 2014-15)
                PRACTICAL-I: Multistage Organic Synthesis (3 & 4 stage)
     (Any five experiments must be carryout)          Max. Marks: 70 (60Prac. + 10Rec.)
Expt-1: Synthesis of paracetomol from benzene
       Step 1: Benzene to Nitrobenzene (Nitration)
       Step 2: Nitrobenzene to N-phenyl hydroxylamine (reduction)
       Step 3: N-phenyl hydroxyl amine to p-aminophenol (Rearrangement)
       Step 4: p-amino phenol to p-hydroxy acetanilide/paracetomol(acetylation)
Expt-2: Synthesis of o-chlorobenzoic acid from phthalic acid
       Step 1: Phthalic acid to phthalic anhydride (Dehydration)
       Step 2: Phthalic anhydride –phthalic amide (Amide formation)
       Step 3: Phthalmide- Anthranilic acid (Hoffman’s Bromamide reaction)
       Step 4: Anthranilic acid -ortho-chloro benzoic acid
Expt-3: Synthesis of sulpha drug from aniline
       Step 1: Aniline to acetanilide
       Step 2: Acetanilide to p-acetamide benzene sulphonyl chloride (sulphonation)
       Step 3: p-acetamide benzenesulphonylchloride to p-acetamide benzenesulphonamide
                                                                             (s-amination)
       Step 4: p-acetamide benzene sulphonamide to p-amino benzenesulphonamide(hydrolysis)
Expt-4: m-Chloro-nitrobenzene from nitrobenzene
       Step 1: Nitro benzene to m-dinitro benzene (nitration)
       Step 2: m-dinitrobenzene to m-nitro aniline (partial reduction)
       Step 3: m-nitro aniline to m-nitrodiazoniumchloride (diazotization)
       Step 4: m-nitrodiazoniumchloride to m-Chloro-nitrobenzene (sandmayers reaction)
Expt-5: Synthesis of p-bromo benzanilide from benzophenone
       Step 1: Benzophenone to benzopenone oxime (Addition)
       Step 2: Benzophenone oxime to benzanilide (Beckman’s rearrangement)
       Step 3: Benzanilide to p-bromobenzanilide) (bromination)
Expt-6: Synthesis of Methyl orange from aniline
       Step 1: Aniline to sulphonic acid (sulphonation)
       Step 2: sulphonic acid to Diazonium chloride (diazotization)
       Step 3: Diazonium chloride to methyl orange (coupling reaction)
Expt-7: Synthesis of Acridone from Anthranilic acid
       Step 1: Anthraninilc acid to o-chlorobenzoic acid (Diazotosation followed by sand
       mayer’s reaction)
       Step 2: o-chlorobenzoic acid to N-phenyl anthranilic acid (Substitution)
       Step 3: N-phenyl anthranilic acid to acridone (Cyclisation)
      All the students must submit the TLC for all the stages of preparation and a photo
copy must be pasted in records.
REFERENCES:
   1. Practical Organic Chemistry A.I.Vogel (Longmans)
   2. Text Book of practical organic Chemistry F.G.Mann & B.C. Sanders.
   3. A Manual of Practical Organic Chemistry Day Sitaramam & Govindachari
   4. Organic Experiments L.F.Fieser.
   5. Practical Organic Chemistry H.T.Openshaw
   6. Systematic Identification of Organic Compounds, P.L.Shriner, R.C.Fuson & D.Y.Curtin.
   7. Identification of Organic Compounds N.D.Cheronis & J.B.Entrilkin
   8. Advanced Organic Synthesis by R.S.Monson Academic Press
       Note: For University Practical Examination: Duration: 9 hours
                                   PRACTICAL – II :: Estimations
 (All experiments must be carryout)                Max. Marks: 70 (15 QA+45Prac.+10Rec.)
Part I: One theory question either relating to spectral characterization or any practical or
        as wish by the examiner.                                               15M
Part II: The following Estimations/Isolations                                      45M
       Expt. 1: Estimation of hydroxyl group by acetylation or pthalation method
       Expt. 2: Estimation of phenol (bromination method)
       Expt. 3: Estimation of aniline (Bromination method)
       Expt. 4: Estimation of carbonyl groups (Hydrazone formation method)
       Expt. 5: Estimation of sugars –glucose and sucrose by using Fehlings solution
       Expt. 6: Determination of iodine value of oil or fat
       Expt. 7: Determination of saponification value of oil or fat
       Expt. 8: Estimation of vitamin ‘C’ in lime juice.
       Expt. 9: Isolation of caffeine from tea/coffee sample.
Record:                                                                                  10M
       For University Practical Examination: Duration: 9 hours
                  Course: M.Sc.; Specialization: ORGANIC CHEMISTRY
                           Practical Syllabus (Semester: IV; Batch: 2014-15)
                     PRACTICAL-I: Analysis of Binary Organic Mixture
  (Any five experiments must be carryout)             Max. Marks: 70 (15QA+45Prac.+10Rec.)
Part I: One theory question either relating to spectral characterization or any practical or
        as wish by the examiner.                                               15M
Part II: Two component organic mixture analysis
    (The student must be given training in at least eight mixtures with different functional
    groups)
       [Note: For University examinations the student has to submit at least two derivatives for each
       individual component].
       NOTE: For University Practical Examination: Duration: 9 hours.
                  Course: M.Sc.; Specialization: ORGANIC CHEMISTRY
                           Practical Syllabus (Semester: IV; Batch: 2014-15)
                        PRACTICAL-II:           Project Work/Home Paper
                                                                       Max. Marks: 100
Project Work / Internship is compulsory for the University students.
Selection of Home Paper/Project Work is optional for affiliated college students.
      The students opted for Home Paper must be assigned a latest topic and the students
       have to submit a dissertation (50-60 pages) covering all the latest literature on the
       topic assigned. The candidate will be assessed at the time of the conduct of final
       practical examination of the semester taking into consideration of dissertation and
       viva-voce on the topic chosen for home paper.