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CHM305Sciences3 Unitsintermediate

Organic Chemistry Iii

This course introduces students to advanced concepts in organic chemistry, focusing on the structure, properties, and reactions of alcohols, ethers, epoxides, carboxylic acids, and carbonyl compounds. It explores nomenclature, preparation methods, and reaction mechanisms, emphasizing practical applications. The course also covers the synthesis and analysis of important organic molecules, providing a solid foundation for further studies in chemistry and related fields. Students will develop problem-solving skills and critical thinking abilities through assignments and laboratory exercises.

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150h
Study Time
13
Weeks
12h
Per Week
basic
Math Level
Course Keywords
AlcoholsEthersCarboxylic AcidsAldehydesSpectroscopy

Course Overview

Everything you need to know about this course

Course Difficulty

Intermediate Level
Builds on foundational knowledge
65%
intermediate
➕
Math Level
Basic Math
🔬
Learning Type
Hands-on Practice

Course Topics

Key areas covered in this course

1

Alcohol Chemistry

2

Ether Synthesis

3

Carboxylic Acid Reactions

4

Aldehyde and Ketone Preparation

5

Spectroscopy in Organic Chemistry

6

Reaction Mechanisms

Total Topics6 topics

Ready to Start

No specific requirements needed

This course is designed to be accessible to all students. You can start immediately without any prior knowledge or specific preparation.

Assessment Methods

How your progress will be evaluated (3 methods)

Assignments

Comprehensive evaluation of course material understanding

Written Assessment

Tutor-Marked Assignments

Comprehensive evaluation of course material understanding

Written Assessment

Final Examination

Comprehensive evaluation of course material understanding

Written Assessment

Career Opportunities

Explore the career paths this course opens up for you

Pharmaceutical Chemist

Apply your skills in this growing field

Chemical Engineer

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Research Scientist

Apply your skills in this growing field

Quality Control Analyst

Apply your skills in this growing field

Biochemist

Apply your skills in this growing field

Industry Applications

Real-world sectors where you can apply your knowledge

PharmaceuticalsPetrochemicalsFood ScienceCosmeticsEnvironmental Science

Study Schedule Beta

A structured 13-week journey through the course content

Week
1

Module 1: Alcohols and Their Reactions

3h

Unit 1: Classes, Structures and Naming Of Alcohols

3 study hours
  • •Read the introduction to alcohols, focusing on their structure and properties.
  • •Practice naming alcohols using both common and IUPAC nomenclature.
  • •Solve problems classifying alcohols into primary, secondary, and tertiary types.
Week
2

Module 1: Alcohols and Their Reactions

3h

Unit 2: Preparation of Alcohols

3 study hours
  • •Study the different methods of preparing alcohols, including hydrolysis and hydration.
  • •Write out reaction equations for each preparation method, noting the conditions.
  • •Discuss the production of alcohol from fermentation.
Week
3

Module 1: Alcohols and Their Reactions

4h

Unit 3: Reactions of Alcohols

4 study hours
  • •Understand the acidity of alcohols compared to water.
  • •Explain the amphoteric nature of alcohols.
  • •Discuss the various reactions of alcohols, stating the necessary conditions of reaction.
Week
4

Module 2: Ethers and Epoxides

3h

Unit 1: Structures and Nomenclature of Ethers and Epoxides

3 study hours
  • •Write the general formula of ethers and epoxides.
  • •Draw the structures of ethers and epoxides.
  • •Distinguish between symmetrical and unsymmetrical ethers.
  • •Write the names of ethers using the IUPAC nomenclature.
  • •State and draw the various isomers of ethers.
Week
5

Module 2: Ethers and Epoxides

4h

Unit 2: Ethers: Preparation and Properties

4 study hours
  • •Discuss the various methods of preparing ethers in the laboratory and industrially.
  • •Explain the various reactions of ethers.
  • •Practice writing out the reactions of ethers.
Week
6

Module 2: Ethers and Epoxides

3h

Unit 3: Epoxides- Preparation and Reactions

3 study hours
  • •Discuss the preparation of epoxides using different methods.
  • •Discuss the physical properties of epoxides.
  • •Discuss the chemical properties of epoxides.
Week
7

Module 3: Carboxylic Acids and Their Derivatives

3h

Unit 1: Carboxylic Acids and Their Derivatives -Naming and Physical properties

3 study hours
  • •Define carboxylic acids.
  • •Give examples of carboxylic acids.
  • •Name and draw the structures of simple carboxylic acid.
  • •Name and draw structures of carboxylic acid derivatives.
  • •Explain the properties of carboxylic acids.
Week
8

Module 3: Carboxylic Acids and Their Derivatives

4h

Unit 2: Preparation of Carboxylic Acids

4 study hours
  • •Prepare carboxylic acids from aldehydes and ketones using oxidation reaction.
  • •Explain preparation of carboxylic acids from hydrolysis of nitriles.
  • •Explain preparation of carboxylic acids from the hydrolysis
Week
9

Module 3: Carboxylic Acids and Their Derivatives

4h

Unit 4: Reactions of Carboxylic Acids

4 study hours
  • •Explain the acidic properties of carboxylic acids.
  • •Discuss the reactions of carboxylic acid has an acid.
  • •Explain the following reactions of carboxylic acids: Esterification, Halogenations.
  • •Explain how esters are converted into: Acyl chloride, Amide, Acid anhydrides.
  • •Explain the reduction of carboxylic acids.
Week
10

Module 3: Carboxylic Acids and Their Derivatives

4h

Unit 5: Derivatives of Carboxylic Acids

4 study hours
  • •Identify the structures of the various derivatives of carboxylic acids.
  • •Compare the properties and reactions of the various derivatives of carboxylic acids.
  • •Explain the reaction of acyl chloride, acid anhydrides, amides and esters
Week
11

Module 4 :Aldehydes and Ketones

3h

Unit 1: Naming Aldehydes and Ketones, Physical Properties

3 study hours
  • •Draw the structure of a simple aldehyde and ketone.
  • •Give the names of aldehydes and ketones from the structures.
  • •State the physical properties of aldehydes and ketones.
  • •Compare the physical properties of the carbonyl compounds
Week
12

Module 4 :Aldehydes and Ketones

4h

Unit: 2 Preparation of Aldehydes and Ketones

4 study hours
  • •Prepare aldehydes and ketones from the dehydration of alcohols.
  • •Prepare aldehydes and ketones from oxidation of alcohols.
  • •Prepare aldehydes and ketones from the oxidation cleavage of alkene.
  • •Prepare aldehydes and ketones from decarbonylation of calcium salts.
  • •Prepare aldehydes and ketones from the reduction of acyl chloride.
  • •Prepare aldehydes and ketones from Friedel Craft acylation reaction
Week
13

Module 4 :Aldehydes and Ketones

4h

Unit 3: Reactions of Aldehydes and Ketones

4 study hours
  • •Explain the acidic properties of carboxylic acids.
  • •Discuss the reactions of carboxylic acid has an acid.
  • •Explain the following reactions of carboxylic acids: Esterification, Halogenations.
  • •Explain how esters are converted into: Acyl chloride, Amide, Acid anhydrides.
  • •Explain the reduction of carboxylic acids

This study schedule is in beta and may not be accurate. Please use it as a guide and consult the course outline for the most accurate information.

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Study Tips & Exam Preparation

Expert tips to help you succeed in this course

1

Create detailed reaction maps for each functional group (alcohols, ethers, carboxylic acids, etc.) linking reactants, reagents, and products.

2

Practice IUPAC nomenclature for complex organic molecules weekly, focusing on identifying parent chains and substituents.

3

Review reaction mechanisms from Units 3-5, drawing out each step and explaining the role of catalysts and intermediates.

4

Solve all Tutor-Marked Assignments (TMAs) and identify areas of weakness for focused study.

5

Create flashcards for key reagents and their specific functions in organic reactions.

6

Dedicate specific study sessions to understanding spectroscopic data (IR, NMR) and its application in identifying organic compounds.

7

Simulate exam conditions by completing past papers within the time limit.

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