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Advanced Organic Chemistry

Informacje ogólne

Kod przedmiotu: 310-ERS-COZE
Kod Erasmus / ISCED: (brak danych) / (brak danych)
Nazwa przedmiotu: Advanced Organic Chemistry
Jednostka: Wydział Chemii
Grupy: erazmus 2024
Program ERASMUS - Chemia
Punkty ECTS i inne: 3.00 Podstawowe informacje o zasadach przyporządkowania punktów ECTS:
  • roczny wymiar godzinowy nakładu pracy studenta konieczny do osiągnięcia zakładanych efektów uczenia się dla danego etapu studiów wynosi 1500-1800 h, co odpowiada 60 ECTS;
  • tygodniowy wymiar godzinowy nakładu pracy studenta wynosi 45 h;
  • 1 punkt ECTS odpowiada 25-30 godzinom pracy studenta potrzebnej do osiągnięcia zakładanych efektów uczenia się;
  • tygodniowy nakład pracy studenta konieczny do osiągnięcia zakładanych efektów uczenia się pozwala uzyskać 1,5 ECTS;
  • nakład pracy potrzebny do zaliczenia przedmiotu, któremu przypisano 3 ECTS, stanowi 10% semestralnego obciążenia studenta.

zobacz reguły punktacji
Język prowadzenia: angielski
Rodzaj przedmiotu:

obowiązkowe

Wymagania (lista przedmiotów):

Organic Chemistry II 310-ERS-CHOR2E
Spectroscopic Methods in Chemical Analysis 310-ERS-MSA

Założenia (lista przedmiotów):

Organic Chemistry II 310-ERS-CHOR2E
Spectroscopic Methods in Chemical Analysis 310-ERS-MSA

Założenia (opisowo):

Completion of an Organic Chemistry II course (e.g., 310-ERS-CHOR2E) and knowledge of spectroscopic methods in chemical analysis (e.g., 310-ERS-MSA) are required. The student should possess basic knowledge of organic chemistry, enabling them to name and discuss the structure of simple organic compounds and their physical and chemical properties, as well as explain the mechanisms of basic reactions. They should be familiar with and capable of applying fundamental techniques for isolating and purifying organic compounds. The student should also have acquired basic manual skills necessary for laboratory work, and be familiar with and adhere to health and safety regulations. The student should have a basic understanding of spectroscopic methods for identifying organic compounds and be able to apply this knowledge in practice.

Tryb prowadzenia przedmiotu:

w sali

Skrócony opis:

The aim of the course is to familiarize students with the current state of knowledge about the reactions of the various types (radical, ionic, pericyclic, organometallic) taking into account their stereochemical course and to show the relationship between the structure and reactivity of organic compounds

Pełny opis:

Study profile – general academic

Mode of study – full-time

Type of subject – mandatory

Field: Exact and Natural Sciences, Discipline: Chemical Sciences

Year of study/semester – Year 1, second cycle, Summer semester

Prerequisites – Organic Chemistry II, Spectroscopic Methods in Chemical Analysis

Number of instructional hours categorized by form – 25 hours of lectures, 30 hours of laboratory

Teaching methods:

- for lectures: lecture, seminar-style lecture, explanatory consultations

- for laboratories: practical exercises, observations, clarifying talks, consultations

ECTS credits – 3

Student workload balance:

Quantitative indicators – student workload related to activities requiring direct teacher involvement: 61.9 hours, corresponding to 2.5 ECTS points; student workload independent of direct teacher involvement: 50.0 hours, corresponding to 2.0 ECTS points.

Literatura:

1. J. Clayden, N. Greeves, S. Warren, P. Wothers "Organic Chemistry",

2. D. G. Morris "Stereochemistry",

3. M. B. Smith, J. March "March's Advanced Organic Chemistry"

4. J. March "Organic Chemistry: reactions, mechanisms, structure"

5. J. McMurry "Organic chemistry"

6. I. Fleming. D. Williams "Spectroscopic Methods in Organic Chemistry"

7. A. I. Vogel "Textbook of Practical Organic Chemistry"

8. L. M. Harwood, C. J. Moody "Experimental Organic Chemistry: Principles and Practice"

Efekty uczenia się:

KP7_WG1 – Knows the types of organic reactions and is able to discuss and represent both basic and complex organic reaction mechanisms graphically, in accordance with the current state of knowledge.

KP7_WG2 – Possesses advanced knowledge in organic chemistry, enabling them to discuss the structure of organic compounds (including their spatial structure), their physical and chemical properties, and explain reaction mechanisms. Knows methods for the synthesis and identification of organic compounds.

KP7_WG7 – Has knowledge of health and safety regulations, particularly the principles of safely handling chemical reagents and solvents, as well as the segregation and disposal of chemical waste. Has the ability to apply this knowledge in laboratory work and organize a safe, independent research workstation.

KP7_UW1 – Is able to plan and conduct scientific experiments in organic compound synthesis, selecting the appropriate amounts of reagents and suitable glassware and laboratory equipment.

KP7_UW2 – Is able to choose and apply appropriate measurement methods to verify the achievement of synthetic goals and use the obtained data to determine the structure of organic compounds.

KP7_UW6 – Has a basic ability to interpret IR, ¹H NMR, and ¹³C NMR spectra. Can compare and interpret data, and apply known solutions to new situations in the synthesis and analysis of organic compounds. Is able to prepare a report on the conducted research.

KP7_KO2 – Can work both in a group and independently. Has knowledge of health and safety regulations and is prepared to create a safe workspace for themselves and other group members.

Metody i kryteria oceniania:

Assessment methods:

a) lecture - written exam,

b) laboratory - reports and written tests from laboratory exercises, chemical equipment quiz, regular assessment of performance during laboratory exercises.

The student is admitted to the exam after successfully completing the laboratory classes. Attendance at lectures is a prerequisite for taking the exam.

The condition for passing the laboratory is attendance at all laboratory exercises and obtaining positive grades for the quiz, report(s), and written test(s).

Assessment criteria according to the approved University of Białystok Study Regulations:

Total points required to achieve the final grade in %:

5 (Very good): 91-100

4+ (Good plus): 81-90

4 (Good): 71-80

3+ (Satisfactory plus): 61-70

3 (Satisfactory): 51-60

2 (Fail): below 51

Flexible forms of assessment may be introduced in agreement between the lecturer and the student, in line with the principles of universal design, provided that these conditions are established at the beginning of the teaching cycle.

Zajęcia w cyklu "Rok akademicki 2023/24" (zakończony)

Okres: 2023-10-01 - 2024-06-30
Wybrany podział planu:
Przejdź do planu
Typ zajęć:
Laboratorium, 30 godzin więcej informacji
Wykład, 25 godzin więcej informacji
Koordynatorzy: Ryszard Łaźny
Prowadzący grup: Dorota Czajkowska-Szczykowska, Ryszard Łaźny
Lista studentów: (nie masz dostępu)
Zaliczenie: Przedmiot - Egzamin
Laboratorium - Zaliczenie na ocenę

Zajęcia w cyklu "Rok akademicki 2024/25" (w trakcie)

Okres: 2024-10-01 - 2025-06-30
Wybrany podział planu:
Przejdź do planu
Typ zajęć:
Laboratorium, 30 godzin więcej informacji
Wykład, 25 godzin więcej informacji
Koordynatorzy: Dorota Czajkowska-Szczykowska
Prowadzący grup: Dorota Czajkowska-Szczykowska
Lista studentów: (nie masz dostępu)
Zaliczenie: Przedmiot - Egzamin
Laboratorium - Zaliczenie na ocenę
Rodzaj przedmiotu:

obowiązkowe

Wymagania (lista przedmiotów):

Organic Chemistry II 310-ERS-CHOR2E
Spectroscopic Methods in Chemical Analysis 310-ERS-MSA

Założenia (lista przedmiotów):

Organic Chemistry II 310-ERS-CHOR2E
Spectroscopic Methods in Chemical Analysis 310-ERS-MSA

Tryb prowadzenia przedmiotu:

w sali

Skrócony opis:

The aim of the course is to familiarize students with the current state of knowledge about the reactions of the various types (radical, ionic, pericyclic, organometallic) taking into account their stereochemical course and to show the relationship between the structure and reactivity of organic compounds

Pełny opis:

The lecture covers the following content:

- Stereochemistry (topicality, prochirality, prostereoisomerism, selectivity and specificity of the reaction, enantiomeric excess and diastereomeric, stereoisomerism of molecules without stereogenic centres).

- Principles of presenting the mechanisms of organic reactions. Radical reactions (chain radical substitution, addition, fragmentation (Hunsdiecker reaction), non-chain radical reactions (Birch reduction, reduction of carbonyl compounds, reactions: pinacol, McMurry, acylin condensation).

- Polar reaction (nucleophilic and electrophilic: mechanism and stereochemistry).

- Selected pericyclic reactions.

- Organometallic compounds and their application in organic synthesis.

Laboratory exercises are designed to familiarize the student with various synthesis techniques, purification methods, and organic compound identification methods (1H NMR, 13C NMR, IR).

Literatura:

1. J. Clayden, N. Greeves, S. Warren, P. Wothers "Organic Chemistry",

2. D. G. Morris "Stereochemistry",

3. M. B. Smith, J. March "March's Advanced Organic Chemistry"

4. J. March "Organic Chemistry: reactions, mechanisms, structure"

5. J. McMurry "Organic chemistry"

6. I. Fleming. D. Williams "Spectroscopic Methods in Organic Chemistry"

7. A. I. Vogel "Textbook of Practical Organic Chemistry"

8. L. M. Harwood, C. J. Moody "Experimental Organic Chemistry: Principles and Practice"

Opisy przedmiotów w USOS i USOSweb są chronione prawem autorskim.
Właścicielem praw autorskich jest Uniwersytet w Białymstoku.
ul. Świerkowa 20B, 15-328 Białystok tel: +48 85 745 70 00 (Centrala) https://uwb.edu.pl kontakt deklaracja dostępności mapa serwisu USOSweb 7.1.1.0-2 (2024-11-25)