GET LIFETIME ACCESS TO ALL OUR COURSES FOR ONLY £199 £99 GET NOW
Take This Course
- £21.00
- 1 year
- Intermediate
- Course Certificate
- Number of Units82
- Number of Quizzes0
- 12 hours, 26 minutes Gift this course
Overview:
Dive into the world of organic chemistry with the Complete Organic Chemistry Demystified course. This course will provide you with an overall idea of organic chemistry. Within no time, you will be able to build a solid foundation in this area.
Through this Complete Organic Chemistry Demystified course, you will learn how to draw organic molecules. The informative modules will educate you on acid-base reactions. You will develop an in-depth understanding of geometry, nomenclature, conformations and more. In addition, you will receive detailed lessons on substitute reactions and elimination reactions. This course will also educate you on synthetic techniques.
This Complete Organic Chemistry Demystified course is the perfect place to explore different aspects of organic chemistry. If you aspire to pursue a career in the relevant fields, this course is the ideal training ground for you. Enrol now!
Please note: Our Complete Organic Chemistry Demystified course only gives you the theoretical knowledge to excel in this field. This course doesn’t entitle you to practise as a professional in this specific field.
Learning Objectives
- Get introduced to the basic steps of drawing organic molecules
- Enrich your knowledge of acid-base relations
- Learn the principles of geometry and nomenclature
- Develop a clear understanding of conformations
- Deepen your understanding of substitute reactions and elimination reactionsGain in-depth knowledge of synthetic techniques
Who is this Course for?
This Complete Organic Chemistry Demystified course is ideal for aspiring professionals or those who wish to gain the relevant skills and knowledge to fast track their careers. It is for those who have little or no knowledge of the principles of organic chemistry or those who are new to the field and want to test their skills and knowledge. There are no entry requirements for this course; however, an eye for detail and a creative mind is essential.
Entry Requirement
- This course is available to all learners of all academic backgrounds.
- A good understanding of the English language, numeracy, and ICT are required to attend this course.
CPD Certificate from Course Gate
At the successful completion of the course, you can obtain your CPD certificate from us. You can order the PDF certificate for £4.99 and the hard copy for £9.99. Also, you can order both PDF and hardcopy certificates for £12.99.
Career path
Upon successfully completing the Complete Organic Chemistry Demystified course, learners can progress to a more advanced program from our course list. Career opportunities in this field include freelancing or working in-house, within a range of professional settings, with the opportunity to earn a high salary. Related professions in this industry include:
- Chemistry teacher
- Food scientist
- Forensic analyst
- Environmental scientist
- Materials scientist
- Analytical chemist
- Pharmacologist
Course Curriculum
| Module 01: About the Course | |||
| Introduction | 00:02:00 | ||
| Module 02: Drawing Organic Molecules | |||
| How to read bond-line drawings | 00:18:00 | ||
| How to draw bond-line drawings | 00:18:00 | ||
| Identifying formal charges | 00:22:00 | ||
| Finding lone pairs that are not drawn | 00:23:00 | ||
| Module 03: Resonance | |||
| What is resonance? | 00:05:00 | ||
| Drawing resonance structures (part 1) | 00:40:00 | ||
| Formal charges in resonance structures | 00:19:00 | ||
| Drawing resonance structures (part 2) | 00:25:00 | ||
| Recognizing patterns | 00:30:00 | ||
| The relative importance of resonance structures | 00:19:00 | ||
| Module 04: Acid-Base Reactions | |||
| Introduction to acid – base | 00:03:00 | ||
| Charged atoms | 00:08:00 | ||
| Resonance | 00:11:00 | ||
| Induction | 00:09:00 | ||
| Orbitals | 00:03:00 | ||
| Charged atoms – Resonance – Induction – Orbitals | 00:07:00 | ||
| Showing an acid-base mechanism | 00:14:00 | ||
| Acid-Base equilibrium position | 00:06:00 | ||
| Module 05: Geometry | |||
| Orbitals | 00:15:00 | ||
| Goemetry of orbitals | 00:15:00 | ||
| Impact of resonance on geometry | 00:01:00 | ||
| Module 06: Nomenclature | |||
| Introduction to nomenclature | 00:03:00 | ||
| Functional group | 00:07:00 | ||
| Unsaturation | 00:04:00 | ||
| Parent | 00:09:00 | ||
| Substituents | 00:10:00 | ||
| “cis” – “trans” stereoisomerism | 00:04:00 | ||
| “E” – “Z” stereoisomerism | 00:04:00 | ||
| Localizing substituents in parent chain | 00:12:00 | ||
| From structure to name | 00:20:00 | ||
| Module 07: Conformations | |||
| Introduction to conformations | 00:02:00 | ||
| Newman projection | 00:10:00 | ||
| Relative stability of Newman projections | 00:08:00 | ||
| Drawing chair conformations | 00:02:00 | ||
| Drawing substituents in chair conformations | 00:11:00 | ||
| Ring flipping | 00:10:00 | ||
| Comparing stability of chair conformations | 00:10:00 | ||
| Module 08: Configurations | |||
| Introduction to configurations | 00:01:00 | ||
| Locating stereocenters | 00:04:00 | ||
| Determining the configuration of a stereocenter | 00:18:00 | ||
| Nomenclature | 00:12:00 | ||
| Enantiomers | 00:08:00 | ||
| Diastereomers | 00:05:00 | ||
| Meso compounds | 00:04:00 | ||
| Fischer projections | 00:11:00 | ||
| Module 09: Mechanisms | |||
| Introduction to mechanisms | 00:02:00 | ||
| Nucleophiles and electrophiles | 00:09:00 | ||
| Arrows used for mechanisms | 00:14:00 | ||
| Carbocation | 00:15:00 | ||
| Module 10: Substitution Reactions | |||
| SN1 SN2 mechanisms | 00:10:00 | ||
| Factor #1: the electrophile | 00:06:00 | ||
| Factor #2: the nucleophile | 00:04:00 | ||
| Factor #3: the leaving group | 00:05:00 | ||
| Factor #4: the solvent | 00:05:00 | ||
| Combining all 4 factors | 00:09:00 | ||
| Module 11: Elimination Reactions | |||
| Introduction to elimination reactions | 00:02:00 | ||
| E1 mechanism | 00:08:00 | ||
| E2 mechanism | 00:20:00 | ||
| Module 12: Substitution vs Elimination | |||
| Introduction to substitution vs elimination | 00:03:00 | ||
| Determining the function of the reagent | 00:04:00 | ||
| Identifying the mechanism(s) | 00:11:00 | ||
| Predicting regiochemical and stereochemical outcomes | 00:16:00 | ||
| Module 13: Addition Reactions | |||
| Introduction to addition reactions | 00:01:00 | ||
| Regiochemistry | 00:05:00 | ||
| Stereochemistry | 00:18:00 | ||
| Hydrogenation: adding H-H | 00:07:00 | ||
| Hydrohalogenation: adding hydrogen halide, H-X | 00:09:00 | ||
| Hydrobromination : adding H-Br | 00:09:00 | ||
| Hydration: adding H-OH | 00:12:00 | ||
| Adding Br and Br | 00:05:00 | ||
| Halohydrin formation: adding Br and OH | 00:08:00 | ||
| “Anti” dihydroxylation: adding OH and OH | 00:07:00 | ||
| “syn” dihydroxylation : adding OH and OH | 00:04:00 | ||
| Ozonolysis | 00:03:00 | ||
| Reactions summary | 00:01:00 | ||
| Module 14: Synthesis Techniques | |||
| One-step synthesis | 00:03:00 | ||
| Combining reactions: changing the position of a leaving group | 00:03:00 | ||
| Combining reactions: changing the position of a double bond | 00:02:00 | ||
| Combining reactions: introducing functionality | 00:03:00 | ||
| Module 15: Wrapping Up and Bonus | |||
| Thank you for enrolling and announcing part 2 | 00:01:00 | ||
| Certificate and Transcript | |||
| Order Your Certificates or Transcripts | 00:00:00 | ||
Take This Course
- £21.00
- 1 year
- Intermediate
- Course Certificate
- Number of Units82
- Number of Quizzes0
- 12 hours, 26 minutes Gift this course
Gift this courseShare Link on 
Instructors
