Organic Chemistry Demystified Training
Course Highlights In today’s time, from common household chemicals to foods and drugs, organic chemistry plays a vital role in …
- Course Highlights
In today’s time, from common household chemicals to foods and drugs, organic chemistry plays a vital role in developing most of the chemical parts of our daily life. To understand and gain a better understanding of organic chemistry, our Organic Chemistry Demystified Training will be the perfect choice for you.
The Organic Chemistry Demystified Training course provides all the necessary information about organic chemistry to gain expertise in organic chemistry. Our learners will get practical as well as theoretical knowledge of it. Topics covered include organic molecules, geometry, nomenclature, conformations, substitution, and elimination along with detailed narration.
The Organic Chemistry Demystified Training course is a self-paced course, meaning the learner can complete the course at his suitable schedule. Our course is split into [number] units with many short modules each under it. We provide professional certificates to the learners after the successful completion of their course.
Join in today to build your skills and meet your competitors head-on!
- Who is This Course For?
Organic Chemistry Demystified Training is ideal for newbie or existing students of organic chemistry, a Chemist, Chemical engineer or professionals working in a chemical related career field. The course is also suitable for individuals who want to broaden or polish their knowledge of organic chemistry
Course Curriculum
Course Curriculum
| Unit 01: About the Course | |||
| Introduction | 00:02:00 | ||
| Unit 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 | ||
| Unit 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 | ||
| Unit 04: Acid-Base Reactions | |||
| Introduction to acid-base reactions | 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 | ||
| Unit 05: Geometry | |||
| Orbitals | 00:03:00 | ||
| Goemetry of orbitals | 00:15:00 | ||
| Impact of resonance on geometry | 00:01:00 | ||
| Unit 06: Nomenclature | |||
| Introduction to Nomenclature | 00:03:00 | ||
| Functional group | 00:07:00 | ||
| Unsaturation | 00:04:00 | ||
| Parent | 00:06:00 | ||
| Substituents | 00:10:00 | ||
| “cis” – “trans” stereoisomerism | 00:04:00 | ||
| “cis” – “trans” stereoisomerism | 00:04:00 | ||
| Localizing substituents in parent chain | 00:12:00 | ||
| From structure to name | 00:20:00 | ||
| Unit 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 | 00:12:00 | ||
| Ring flipping | 00:10:00 | ||
| Comparing stability of chair conformations | 00:10:00 | ||
| Unit 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 | ||
| Unit 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 | ||
| Unit 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 | 00:04:00 | ||
| Factor #4: the solvent | 00:05:00 | ||
| Combining all 4 factors | 00:10:00 | ||
| Unit 11: Elimination Reactions | |||
| Introduction to elimination reactions | 00:02:00 | ||
| E2 mechanism | 00:20:00 | ||
| E1 mechanism | 00:08:00 | ||
| Unit 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 | ||
| Unit 13: Addition Reactions | |||
| Introduction to addition reactions | 00:01:00 | ||
| Regiochemisty | 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 | ||
| Unit 14: Synthesis Techniques | |||
| One-step synthesis | 00:03:00 | ||
| Combining reactions: changing the position of a double bond | 00:10:00 | ||
| Combining reactions: changing the position of a double bond | 00:10:00 | ||
| Combining reactions: introducing functionality | 00:03:00 | ||
| Unit 15: Wrapping Up and Bonus | |||
| Thank you for enrolling and announcing part 2 | 00:01:00 | ||
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1 Year Access 
5 Students 
12 hours, 27 minutes