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midterm organic chemistry 232-English

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Giảng viên ra đề: (Ngày ra đề) Người phê duyệt: (Ngày duyệt đề)

Trưởng bộ môn Kỹ thuật Hóa hữu cơ


PGS. TS. Lê Thị Hồng Nhan

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

MIDTERM EXAM Semester/year 2 2023-2024


Date 16/03/2024
Course Organic Chemistry
Ho Chi Minh City University of Technology Course No. CH2021
(HCMUT), VNU-HCM
FACULTY OF CHEMICAL ENGINEERING Duration 60 min Code 02
Notes: - Materials, cell phones, or any communication devices are not allowed.
- Only the answers in the corresponding boxes are accepted.
Proctor 1 (Giám thị 1) Proctor (Giám thị 2)

Question 1) (L.O.1, 1.0 pt): Indicate the number of asymmetric carbons and the absolute configuration
of two carbons numbered in the following structure.

Question Answer
i) How many asymmetric carbons are
there in the given structure? (0.5 pt)

Carbon 1: …..
ii) What are the absolute configurations
of carbons 1 and 2? (0.5 pt)
Carbon 2: …..

Question 2) (L.O.1, 1.0 pt): Indicate the absolute configuration of six carbons numbered in the following
compounds.

0.5 pt 0.5 pt

Carbon 3 4 5 6 7 8

Absolute configuration

Student ID:............................. Student name:.....................................Page 1/7-Code: 02


Question 3 (L.O.1, 0.5 pt): Arrange four following compounds in the order of decreasing basicity.

Answer: …… > …… > …… > ……

Question 4 (L.O.1, 0.5 pt): Arrange eight following compounds in the order of decreasing acidity.

Answer: …… > …… > …… > …… > …… > …… > …… > ……

Student ID:............................. Student name:.....................................Page 2/7-Code: 02


Question 5 (L.O.1, 0.5 pt): Which of the following structures is/are AROMATIC?

Answer:

Question 6 (L.O.1, 0.5 pt): Which of the following structures is/are AROMATIC?

Answer:

Student ID:............................. Student name:.....................................Page 3/7-Code: 02


Question 7 (L.O.2, 1.5 pt): What is the structure of the product(s) in each of the following reaction?
NO STEREOCHEMISTRY IS REQUIRED.
Answer:

Answer:

Answer:

Student ID:............................. Student name:.....................................Page 4/7-Code: 02


Question 8 (L.O.2, 1.5 pt): What is the structure of the product(s) in each of the following reaction?
STEREOCHEMISTRY MUST BE SHOWN IF NECESSARY.

Answer:
Product(s) MUST be presented by perspective
formula(s).

Product(s) MUST be presented by perspective


formula(s).

Answer:
Product(s) MUST be presented by perspective
formula(s).

Product(s) MUST be presented by perspective


formula(s).

Answer:
Product(s) MUST be presented by perspective
formula(s).

Product(s) MUST be presented by perspective


formula(s).

Student ID:............................. Student name:.....................................Page 5/7-Code: 02


Question 9 (L.O.3, 2 pt): What is the structure of compounds (A), (B), (C), and (D) respectively in the
following reaction sequences? NO STEREOCHEMISTRY IS REQUIRED.

Answer:

(A) (B)

(C) (D)

Student ID:............................. Student name:.....................................Page 6/7-Code: 02


Question 10 (L.O.3, 1 pt): Complete the following transformation with detailed reactions and conditions
by using the pool of chemicals: but-1-en-3-yne (CH≡C-CH=CH2), cyclohex-2-ene-1,4-dione, Na, Br2, H2,
NH3, KOH, Ni, N2H4, H2O. No other chemicals are accepted. The application of ultraviolet light and
heating is allowed if necessary. NO STEREOCHEMISTRY IS REQUIRED.

Note that a ketone (C=O) can react with H2 in the presence of an Ni catalyst to form an alcohol (-CH-
OH).
Answer:

THIS IS THE END OF THE EXAM.

Student ID:............................. Student name:.....................................Page 7/7-Code: 02

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