Overview

This second-year chemistry unit is designed for students who have completed introductory organic chemistry as part of their first-year studies. It focuses on advancing students’ knowledge in key areas of organic chemistry, including organic reactions, stereochemistry, and synthetic strategies. The unit also builds on foundational laboratory techniques, enhancing students’ practical skills in organic chemistry. Through this unit, students will deepen their understanding and develop specialized expertise in organic chemistry, preparing them for further study and research in the field.

Requisites

Prerequisites
CHE10002 Chemistry 2
Teaching periods
Location
Start and end dates
Last self-enrolment date
Census date
Last withdraw without fail date
Results released date
Semester 2
Location
Hawthorn
Start and end dates
04-August-2025
02-November-2025
Last self-enrolment date
17-August-2025
Census date
31-August-2025
Last withdraw without fail date
19-September-2025
Results released date
09-December-2025
Semester 2
Location
Hawthorn
Start and end dates
03-August-2026
01-November-2026
Last self-enrolment date
16-August-2026
Census date
01-September-2026
Last withdraw without fail date
22-September-2026
Results released date
08-December-2026

Learning outcomes

Students who successfully complete this unit will be able to:

  • Interpret fundamental concepts including electrophiles/nucleophiles, acidity/basicity, and apply curly arrow notation to rationalize organic reaction mechanisms
  • Explain and apply key reaction mechanisms including aliphatic nucleophilic substitution, aromatic electrophilic substitution and key carbonyl reactions, to predict reaction outcomes and product distributions
  • Analyze the stereochemistry of organic molecules and accurately distinguish between various types of stereoisomers
  • Design organic synthetic pathways by applying strategies of functional group interconversion and retrosynthetic analysis
  • Demonstrate a thorough understanding of polymer chemistry, including polymer classification and methods of synthesis
  • Exhibit proficiency in organic laboratory techniques and effectively communicate experimental results through structured scientific reports

Teaching methods

Hawthorn

Type Hours per week Number of weeks Total (number of hours)
Live Online
Lecture
1.00  12 weeks  12
On-campus
Lecture
1.00 12 weeks 12
On-campus
Lab
3.00  12 weeks  36
Unspecified Activities
Independent Learning
7.50  12 weeks  90
TOTAL     150

Assessment

Type Task Weighting ULO's
Online Assignment Individual  5 - 10%  1
Examination Individual  20 - 35%  3.4.5
Laboratory Report Individual/Group  35 - 50%  6
Mid-Semester Test Individual  20 - 30%  1,2

Hurdle

As the minimum requirements of assessment to pass a unit and meet all ULOs to a minimum standard, an undergraduate student must have achieved:

(i) an aggregate mark of 50% or more, and
(ii) obtain at least 40% in the final exam, and must
(iii) obtain at least 40% of the possible marks for the laboratory hurdle.

Students who do not successfully achieve hurdle requirements (ii) and (iii) will receive a maximum of 45% as the total mark for the unit.

Content

  • Fundamental concepts of electrophiles and nucleophiles, acidity and basicity
  • Curly arrow notation for illustrating electron movement in organic reaction mechanisms
  • Core organic reactions including aliphatic nucleophilic substitution, aromatic electrophilic substitution, carbonyl compound reactions
  • Principles of stereochemistry and classification of stereoisomers
  • Strategies in organic synthesis, including functional group interconversion and polymer synthesis
  • Advanced practical techniques in organic chemistry laboratories

Study resources

Reading materials

A list of reading materials and/or required textbooks will be available in the Unit Outline on Canvas.