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Overview
By enroling in Organic Chemistry Demystified, you can kickstart your vibrant career and strengthen your profound knowledge. You can learn everything you need to know about the topic.
The Organic Chemistry Demystified course includes all of the most recent information to keep you abreast of the employment market and prepare you for your future. The curriculum for this excellent Organic Chemistry Demystified course includes modules at all skill levels, from beginner to expert. You will have the productivity necessary to succeed in your organisation once you have completed our Organic Chemistry Demystified Program.
So enrol in our Organic Chemistry Demystified course right away if you’re keen to envision yourself in a rewarding career.
Description
Enroling in this Organic Chemistry Demystified course can improve your Organic Chemistry Demystified perspective, regardless of your skill levels in the Organic Chemistry Demystified topics you want to master. If you’re already a Organic Chemistry Demystified expert, this peek under the hood will provide you with suggestions for accelerating your learning, including advanced Organic Chemistry Demystified insights that will help you make the most of your time. This Organic Chemistry Demystified course will act as a guide for you if you’ve ever wished to excel at Organic Chemistry Demystified.
Why Choose Us?
- After successfully completing the Organic Chemistry Demystified Course, you will receive a FREE PDF Certificate as evidence of your newly acquired abilities.
- Lifetime access to the whole collection of Organic Chemistry Demystified learning materials.
- Online test with immediate results
- Enroling in the course has no additional cost.
- You can study and complete the Organic Chemistry Demystified course at your own pace.
- Study for the Organic Chemistry Demystified course using any internet-connected device, such as a computer, tablet, or mobile device.
Who Is This Course For?
This Organic Chemistry Demystified course is a great place to start if you’re looking to start a new career in Organic Chemistry Demystified field. This training is for anyone interested in gaining in-demand Organic Chemistry Demystified proficiency to help launch a career or their business aptitude.
Requirements
The Organic Chemistry Demystified course requires no prior degree or experience. All you require is English proficiency, numeracy literacy and a gadget with stable internet connection. Learn and train for a prosperous career in the thriving and fast-growing industry of Organic Chemistry Demystified, without any fuss.
Career Path
This Organic Chemistry Demystified training will assist you develop your Organic Chemistry Demystified ability, establish a personal brand, and present a portfolio of relevant talents. It will help you articulate a Organic Chemistry Demystified professional story and personalise your path to a new career. Furthermore, developing this Organic Chemistry Demystified skillset can lead to numerous opportunities for high-paying jobs in a variety of fields.
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 | 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 | 00:15:00 | ||
| 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 | 00:09:00 | ||
| 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 | ||
| 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 | 00:05:00 | ||
| 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 | ||
| E1 mechanism | 00:08:00 | ||
| E2 mechanism | 00:20:00 | ||
| 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 | ||
| 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 | ||
| Unit 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 | ||
| Unit 15: Wrapping Up and Bonus | |||
| Thank you for enrolling and announcing part 2 | 00:01:00 | ||
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