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Organic Chemistry Demystified

Course Overview

You’ll have an arsenal of skills to lock down your desired career after completing this Organic Chemistry Demystified course. Moreover, you will have access to all of the materials in this course for free for a whole year and learn a multitude of highly coveted skills to move up the corporate ladder.

With this comprehensive Organic Chemistry Demystified course, you’ll have all of your questions answered and all of the necessary expertise under your belt. Apart from setting you up for success, this course offers numerous advantages to make your learning experience more pleasurable and less stressful. So, add this Organic Chemistry Demystified course to the basket and take your expertise up a notch!

Please Note: Thames College is a One Education approved resale partner for Quality Licence Scheme Endorsed courses.

Why Choose Thames College?

Thames College offers you the benefit of —

Who Is This Course For?

Those who want to strengthen their professional skills while training for the desired job should take advantage of the Organic Chemistry Demystified training! This course will keep you up-to-date with all the latest developments and coach you accordingly. So invest in this Organic Chemistry Demystified course if you want the best training available.

Certificate of Achievement

CPD Certification

After successfully completing the assessment of this Organic Chemistry Demystified course, you will be eligible for a Free CPD Certificate. You can also get a Printed Hardcopy for only 2.99 GBP.

Requirements

No formal entry requirements! No prerequisites or relevant experience is required!

This course is accessible to anyone with an eagerness to learn. All you require is—

Career Path

Utilise this all-inclusive course to acquire the skills and expertise you’ll need to thrive in the workplace.

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
Assignment
Assignment -Organic Chemistry Demystified 00:00:00

Certificate of Achievement

CPD Accredited Certification

You will be eligible for CPD Accredited Certificates after completing this Course successfully.
Certification is available –
  1. In PDF for £2.99
  2. Hard copy for £8.99
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