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BSc Chemistry (Hons.) Semester-IV (Jan.-June, 2021)
First Internal Assessment Test: 17-07-2021
Subject: Organic Chemistry Paper: C10T
Full Marks: 10 Exam. Hours: 10:00 AM to 10:30 AM
Candidates are required to give answers in their own words and briefly
as far as practicable. Questions are of equal value. All parts of a question
must be attempted together.
Submit pdf of Answer paper to: satyajit@tmv.ac.in
• Please Write the following on top of the first page of the Answer
Papers:
Name: ______________________________Sem-IV Chemistry (Hons) FM: 10
Univ. Roll____________No._______________Regn. No._______________Session___________
• Please use the PDF file name in the Format: Your First Name-Sem-
IV-Hons-1st Internal Assessment Test, 17-07-2021
Nitrogen Compounds and Rearrangements
Answer any five questions 5 x 2 = 10
Q.1 Suggest mechanism and stereo-chemical outcome of the following
reaction.
Q.2 Identify the starting material of the following Claisen rearrangement
reaction.
TAMRALIPTA MAHAVIDYALAYA
DEPARTMENT of CHEMISTRY
Tamluk :: Purba Medinipur :: 721636
Page 2 of 2
Q.3 Identify the products X and Y of the following reactions sequence.
Q.4 In the following Beckman rearrangement, two isomeric products are
possible. Draw them. Explain which one is formed and why?
Q.5 Write down the mechanism of the following reaction.
Q.6 Identify the products A and B that might be formed in the following
reactions sequence:
Q.7 What is Henry reaction? Show its mechanism.
Q.8 Explain the following differences
*** End ***
Page 1 of 2
BSc Chemistry (Hons.) Semester-IV (Jan.— June, 2021)
Second Internal Assessment Test: 22-07-2021
Subject: Organic Chemistry Paper: C10T
Full Marks: 10 Exam. Time: 10:00 AM to 10:30 AM
Candidates are required to give answers in their own words and
briefly as far as practicable. Questions are of equal value. All parts
of a question must be attempted together.
Submit pdf of Answer paper to: satyajit@tmv.ac.in
• Please Write the following on top of the first page of the Answer
Papers:
Name: ______________________________Sem-IV Chemistry (Hons) FM: 10
Univ. Roll____________No._______________Regn. No._______________Session___________
The Logic of Organic Synthesis and Organic Spectroscopy
Answer any five questions 5 x 2 = 10
Q.1 π → π* transition shows bathochromic shift in polar protic solvent.
Justify the statement
Q.2 H+ ion shifts the n→ π* transition of C=O to higher energy. Explain.
Q.3 Demonstrate how IR spectroscopy might be used to monitor the progress
of the following reaction.
Q.4 Define the term: Chemical shift.
Q.5 Find out the products A and B of the following reactions sequence.
TAMRALIPTA MAHAVIDYALAYA
DEPARTMENT of CHEMISTRY
Tamluk :: Purba Medinipur :: 721636
Page 2 of 2
Q.6 Show retrosynthesis and proposal of synthesis of the following
molecule (any one)
Q.7 Using protection-deprotection technique how would you carry out the
following transformation
Q.8 Show how “reconnection” technique may be used in synthesis of a
target molecule containing 1,6-dioxygenated functionality.
*** End ***

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Question paper of 1st & 2nd internal assessment test for chemistry hons sem iv

  • 1. Page 1 of 2 BSc Chemistry (Hons.) Semester-IV (Jan.-June, 2021) First Internal Assessment Test: 17-07-2021 Subject: Organic Chemistry Paper: C10T Full Marks: 10 Exam. Hours: 10:00 AM to 10:30 AM Candidates are required to give answers in their own words and briefly as far as practicable. Questions are of equal value. All parts of a question must be attempted together. Submit pdf of Answer paper to: satyajit@tmv.ac.in • Please Write the following on top of the first page of the Answer Papers: Name: ______________________________Sem-IV Chemistry (Hons) FM: 10 Univ. Roll____________No._______________Regn. No._______________Session___________ • Please use the PDF file name in the Format: Your First Name-Sem- IV-Hons-1st Internal Assessment Test, 17-07-2021 Nitrogen Compounds and Rearrangements Answer any five questions 5 x 2 = 10 Q.1 Suggest mechanism and stereo-chemical outcome of the following reaction. Q.2 Identify the starting material of the following Claisen rearrangement reaction. TAMRALIPTA MAHAVIDYALAYA DEPARTMENT of CHEMISTRY Tamluk :: Purba Medinipur :: 721636
  • 2. Page 2 of 2 Q.3 Identify the products X and Y of the following reactions sequence. Q.4 In the following Beckman rearrangement, two isomeric products are possible. Draw them. Explain which one is formed and why? Q.5 Write down the mechanism of the following reaction. Q.6 Identify the products A and B that might be formed in the following reactions sequence: Q.7 What is Henry reaction? Show its mechanism. Q.8 Explain the following differences *** End ***
  • 3. Page 1 of 2 BSc Chemistry (Hons.) Semester-IV (Jan.— June, 2021) Second Internal Assessment Test: 22-07-2021 Subject: Organic Chemistry Paper: C10T Full Marks: 10 Exam. Time: 10:00 AM to 10:30 AM Candidates are required to give answers in their own words and briefly as far as practicable. Questions are of equal value. All parts of a question must be attempted together. Submit pdf of Answer paper to: satyajit@tmv.ac.in • Please Write the following on top of the first page of the Answer Papers: Name: ______________________________Sem-IV Chemistry (Hons) FM: 10 Univ. Roll____________No._______________Regn. No._______________Session___________ The Logic of Organic Synthesis and Organic Spectroscopy Answer any five questions 5 x 2 = 10 Q.1 π → π* transition shows bathochromic shift in polar protic solvent. Justify the statement Q.2 H+ ion shifts the n→ π* transition of C=O to higher energy. Explain. Q.3 Demonstrate how IR spectroscopy might be used to monitor the progress of the following reaction. Q.4 Define the term: Chemical shift. Q.5 Find out the products A and B of the following reactions sequence. TAMRALIPTA MAHAVIDYALAYA DEPARTMENT of CHEMISTRY Tamluk :: Purba Medinipur :: 721636
  • 4. Page 2 of 2 Q.6 Show retrosynthesis and proposal of synthesis of the following molecule (any one) Q.7 Using protection-deprotection technique how would you carry out the following transformation Q.8 Show how “reconnection” technique may be used in synthesis of a target molecule containing 1,6-dioxygenated functionality. *** End ***