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    cuối kỳ đề oisp hk212

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    Man Chung
    This document is an organic chemistry final exam consisting of 5 questions testing students' knowledge of organic reactions, structures, and synthetic tactics. The exam provides reaction sequences and asks students to identify structures, products, and propose multi-step syntheses using limited starting materials. Students are instructed to show their work and provide structures without stereochemistry where specified. The exam is 70 minutes and covers key learning objectives related to organic chemistry principles and synthesis.

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    cuối kỳ đề oisp hk212

    Uploaded by

    Man Chung
    94 views7 pages
    This document is an organic chemistry final exam consisting of 5 questions testing students' knowledge of organic reactions, structures, and synthetic tactics. The exam provides reaction sequences and asks students to identify structures, products, and propose multi-step syntheses using limited starting materials. Students are instructed to show their work and provide structures without stereochemistry where specified. The exam is 70 minutes and covers key learning objectives related to organic chemistry principles and synthesis.

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    cuối-kỳ-đề-oisp-hk212

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    This document is an organic chemistry final exam consisting of 5 questions testing students' knowledge of organic reactions, structures, and synthetic tactics. The exam provides reaction sequences and asks students to identify structures, products, and propose multi-step syntheses using limited starting materials. Students are instructed to show their work and provide structures without stereochemistry where specified. The exam is 70 minutes and covers key learning objectives related to organic chemistry principles and synthesis.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    94 views7 pages

    cuối kỳ đề oisp hk212

    Uploaded by

    Man Chung
    This document is an organic chemistry final exam consisting of 5 questions testing students' knowledge of organic reactions, structures, and synthetic tactics. The exam provides reaction sequences and asks students to identify structures, products, and propose multi-step syntheses using limited starting materials. Students are instructed to show their work and provide structures without stereochemistry where specified. The exam is 70 minutes and covers key learning objectives related to organic chemistry principles and synthesis.

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    You are on page 1of 7

    (Ngày ra đề) (Ngày duyệt đề)

    Giảng viên ra đề: Người phê duyệt:


    (Chữ ký, Chức vụ và Họ tên)

    (phần phía trên cần che đi khi in sao đề thi)

    Semester/year 2 2021-2022
    FINAL EXAM Date 12/06/2022
    Course Organic Chemistry
    Ho Chi Minh City University of Technology Course No. CH2021
    (HCMUT), VNU-HCM
    FACULTY OF CHEMICAL ENGINEERING Duration 70 min Code 01
    Note: - Materials, cell phones, or any communication devices are not allowed.
    - Only the answers in the boxes are accepted.

    Question 1) (L.O.2, 2 points): What is the product for each of the following reaction? NO

    stereochemistry is required.

    Reactions Answers

    Student ID: ............................ Student name: .................................................... Page 1/7


    Question 2) (L.O.1, 2 points): What is the structure of (A), (B), (C), and (D), respectively, in the

    following reaction sequence? Please note that NO stereochemistry is required.

    Answers:

    (A) (B)

    Student ID: ............................ Student name: .................................................... Page 2/7


    (C) (D)

    Question 3) (L.O.1, 2 points): What is the structure of (E), (F), (G), and (H), respectively, in the

    following reaction sequence? Please note that isotopes must be addressed if necessary and NO

    stereochemistry is required.

    Student ID: ............................ Student name: .................................................... Page 3/7


    Answers:

    (E) (F)

    (G) (H)

    Question 4) (L.O.3, 2 points):

    4.1 Propose a synthetic tactic to complete the following transformation (from (A) to (B) as shown below).

    You are ONLY allowed to use the given chemicals: CH3CH2OH, tetrahydrofuran (THF), SOCl2, CO2,

    AlCl3, HCl, H2SO4, NaOH, H2O, Mg, Fe, Zn, and Br2. Reaction temperatures are not limited.

    Student ID: ............................ Student name: .................................................... Page 4/7


    Answer:

    Student ID: ............................ Student name: .................................................... Page 5/7


    4.2 Propose a synthetic tactic to complete the following transformation (from (C) to (D) as shown

    below). You are ONLY allowed to use the given chemicals: CuCN, CH3COCl, NaOH, HCl, H2SO4, H2O,

    HNO3, NaBH4, LiAlH4, Fe, H3PO2, and NaNO2. Reaction temperatures are not limited.

    Answer:

    Student ID: ............................ Student name: .................................................... Page 6/7


    Question 5) (L.O.3, 2 points): What is the product for each of the following reactions? Please note that

    isotopes and stereochemistry must be addressed if necessary.

    Reactions Answers

    You are asked to use Fischer formula to


    present the product(s).

    --- THIS IS THE END OF THE EXAM---

    Student ID: ............................ Student name: .................................................... Page 7/7

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