Become a trained professional from the safety and comfort of your own home by taking Organic Chemistry Demystified . Whatever your situation and requirements, One Education can supply you with professional teaching, gained from industry experts, and brought to you for a great price with a limited-time discount.
One Education has been proud to produce an extensive range of best-selling courses, and Organic Chemistry Demystified is one of our best offerings. It is crafted specially to promote easy learning at any location with an online device. Each topic has been separated into digestible portions that can be memorised and understood in the minimum of time.
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By completing Organic Chemistry Demystified, you will have automatically earnt an e-certificate that is industry-recognised and will be a great addition to your competencies on your CV.
Whatever your reason for studying Organic Chemistry Demystified, make the most of this opportunity from One Education and excel in your chosen field.
Please be aware that there are no hidden fees, no sudden exam charges, and no other kind of unexpected payments. All costs will be made very clear before you even attempt to sign up.
The course is delivered through our online learning platform, accessible through any internet-connected device. There are no formal deadlines or teaching schedules, meaning you are free to study the course at your own pace.
You are taught through a combination of
- Video lessons
- Online study materials
Will I receive a certificate of completion?
Upon successful completion, you will qualify for the UK and internationally-recognised CPD accredited certification. You can choose to make your achievement formal by obtaining your PDF Certificate at the cost of £9 and Hard Copy Certificate for £15.
Why study this course
It doesn’t matter if you are an aspiring professional or absolute beginner; this course will enhance your expertise and boost your CV with critical skills and an accredited certification attesting to your knowledge.
The Organic Chemistry Demystified is fully available to anyone, and no previous qualifications are needed to enrol. All One Education needs to know is that you are eager to learn and are over 16.
|Unit 01: About the Course|
|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|
|The relative importance of resonance structures||00:19:00|
|Unit 04: Acid-Base Reactions|
|Introduction to acid – base||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|
|Goemetry of orbitals||00:15:00|
|Impact of resonance on geometry||00:01:00|
|Unit 06: Nomenclature|
|Introduction to nomenclature||00:03:00|
|“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|
|Relative stability of Newman projections||00:08:00|
|Drawing chair conformations||00:02:00|
|Drawing substituents in chair conformations||00:12:00|
|Comparing stability of chair conformations||00:10:00|
|Unit 08: Configurations|
|Introduction to configurations||00:01:00|
|Determining the configuration of a stereocenter||00:18:00|
|Unit 09: Mechanisms|
|Introduction to mechanisms||00:02:00|
|Nucleophiles and electrophiles||00:09:00|
|Arrows used for mechanisms||00:14:00|
|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|
|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|
|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|
|Unit 14: Synthesis Techniques|
|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 -Organic Chemistry Demystified||00:00:00|
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