Organic Chemistry II

COURSE CURRICULUM

1.

Course title

ORGANIC CHEMISTRY II

2.

Code

HM-403

3.

Study curriculum

Chemistry (applied chemistry, analytical biochemistry)

4.

Organizer of the curriculum (institute, department)

Institute of chemistry, PMF, UKIM

5.

Degree (BSc, MSc, PhD)

BSc

6.

Academic year/semester

II/IV

7.

ECTS points

8

8.

Lecturer

Dr. Emil Popovski, Professor
Dr. Jane Bogdanov, Professor
Dr. Natasa Ristovska, Professor

9.

Prerequisites

Inorganic chemistry and signature from Organic Chemistry I

10.

Course objectives (competences):
The purpose of this course is to introduce the student to the common structural features of organic compounds. The student will get to know the characteristics of organic compounds containing specific functional groups, such as alcohols, phenols, thiols, ethers, aldehydes, ketones, acids, esters, amides, anhydrides, acyl halides, amines, etc. The student will learn how to name and draw the appropriate structures, as well as identify methods for their synthesis. The study will also examine the reactions in which organic compounds participate. Also, the development of the skills in the laboratory work of the student, performing syntheses, isolating and identifying certain organic substances will continue.

11.

Course content:
Benzene and aromaticity (nomenclature of aromatic compounds, structure and stability, molecular orbitals). Chemistry of benzene (characteristic reactions of electrophilic and nucleophilic aromatic substitution, synthesis). Alcohols and phenols (nomenclature, characteristic properties, obtaining, reactions, spectroscopic analysis). Ethers and epoxides (nomenclature, characteristic properties, preparation, reactions, spectroscopic analysis). Thiols and sulfides. Aldehydes and ketones (nomenclature, characteristic properties, preparation, reactions, spectroscopic analysis). Carboxylic acids and nitriles (nomenclature, characteristic properties, preparation, reactions, spectroscopic analysis). Derivatives of carboxylic acids (nomenclature, characteristic properties, preparation, reactions, spectroscopic analysis). Polyamides and polyesters. Substitution reactions of alpha – C atom. Condensation reactions. Amines (nomenclature, characteristic properties, obtaining, reactions, spectroscopic analysis).

12.

Teaching methods: lectures, laboratory classes, problem solving, projects

13.

Total available time

240 hours

14.

Time distribution

4+1+3 hours/week (lectures 60 hours, problem solving 15 hours, laboratory classes 45 hours)

15.

Teaching methods distribution

15.1.

Teaching - lectures

60 hours

15.2.

Practicals (laboratory, problem solving), seminars, team work

60 hours

16.

Other activities

16.1.

Projects

/

16.2.

Independent work

30 hours

16.3.

Homework

90 hours

17.

Grading methods

17.1.

Tests

70 points

17.2.

Seminars/projects (written/oral presentation)

15 points

17.3.

Activity

15 points

18.

Grading scale (points/mark)

< 50 points

5 (five) (F)

51 to 60 points

6 (six) (E)

61 to 70 points

7 (seven) (D)

71 to 80 points

8 (eight) (C)

81 to 90 points

9 (nine) (B)

91 to 100 points

10 (ten) (A)

19.

Criteria for taking the final exam

Finished laboratory practicals and attending lectures

20.

Course language

Macedonian

21.

Teaching quality control

Anonymus surveys for course quality and student suggestions

22.

Literature

22.1.

Compulsory

No.

Author

Title

Publisher

Year

1.

John McMurry

Organic Chemistry 6thed.

Brooks/Cole

2004

2.

Bell C. E.; Taber D. F.; Clark A. K.

Organic chemistry laboratory with qualitative analysis: standard and microscale, 3rd ed.

Thomson

2001

3.

J.G. Traynham

Organic Nomenclature: A Programmed Introduction, 5th ed.

Prentice Hall

1997

22.2.

Additional

No.

Author

Title

Publisher

Year

1.

2.

3.

4.