Overview
This comprehensive course on Organic Chemistry Demystified will deepen your understanding on this topic.
After successful completion of this course you can acquire the required skills in this sector. This Organic Chemistry Demystified comes with accredited certification from CPD, which will enhance your CV and make you worthy in the job market.
So enrol in this course today to fast track your career ladder.
How will I get my certificate?
You may have to take a quiz or a written test online during or after the course. After successfully completing the course, you will be eligible for the certificate.
Who is This course for?
There is no experience or previous qualifications required for enrolment on this Organic Chemistry Demystified. It is available to all students, of all academic backgrounds.
Requirements
Our Organic Chemistry Demystified is fully compatible with PC’s, Mac’s, Laptop, Tablet and Smartphone devices. This course has been designed to be fully compatible with tablets and smartphones so you can access your course on Wi-Fi, 3G or 4G.
There is no time limit for completing this course, it can be studied in your own time at your own pace.
Career Path
Having these various qualifications will increase the value in your CV and open you up to multiple sectors such as Business & Management, Admin, Accountancy & Finance, Secretarial & PA, Teaching & Mentoring etc.
Course Curriculum
- 16 sections
- 82 lectures
- 00:00:00 total length
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Introduction 00:02:00
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How to read bond-line drawings 00:18:00
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How to draw bond-line drawings 00:18:00
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Identifying formal charges 00:22:00
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Finding lone pairs that are not drawn 00:23:00
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What is resonance? 00:05:00
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Drawing resonance structures (part 1) 00:40:00
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Formal charges in resonance structures 00:19:00
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Drawing resonance structures (part 2) 00:25:00
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Recognizing patterns 00:30:00
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The relative importance of resonance structures 00:19:00
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Introduction to acid – base 00:03:00
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Charged atoms 00:08:00
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Resonance 00:11:00
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Induction 00:09:00
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Orbitals 00:03:00
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Charged atoms – Resonance – Induction – Orbitals 00:07:00
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Showing an acid-base mechanism 00:14:00
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Acid-Base equilibrium position 00:06:00
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Orbitals 00:15:00
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Goemetry of orbitals 00:15:00
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Impact of resonance on geometry 00:01:00
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Introduction to nomenclature 00:03:00
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Functional group 00:07:00
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Unsaturation 00:04:00
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Parent 00:09:00
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Substituents 00:10:00
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“cis” – “trans” stereoisomerism 00:04:00
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“E” – “Z” stereoisomerism 00:04:00
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Localizing substituents in parent chain 00:12:00
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From structure to name 00:20:00
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Introduction to conformations 00:02:00
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Newman projection 00:10:00
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Relative stability of Newman projections 00:08:00
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Drawing chair conformations 00:02:00
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Drawing substituents in chair conformations 00:12:00
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Ring flipping 00:10:00
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Comparing stability of chair conformations 00:10:00
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Introduction to configurations 00:01:00
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Locating stereocenters 00:04:00
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Determining the configuration of a stereocenter 00:18:00
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Nomenclature 00:12:00
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Enantiomers 00:08:00
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Diastereomers 00:05:00
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Meso compounds 00:04:00
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Fischer projections 00:11:00
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Introduction to mechanisms 00:02:00
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Nucleophiles and electrophiles 00:09:00
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Arrows used for mechanisms 00:14:00
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Carbocation 00:15:00
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SN1 SN2 mechanisms 00:10:00
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Factor #1: the electrophile 00:06:00
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Factor #2: the nucleophile 00:04:00
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Factor #3: the leaving group 00:05:00
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Factor #4: the solvent 00:05:00
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Combining all 4 factors 00:10:00
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Introduction to elimination reactions 00:02:00
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E1 mechanism 00:08:00
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E2 mechanism 00:20:00
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Introduction to substitution vs elimination 00:03:00
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Determining the function of the reagent 00:04:00
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Identifying the mechanism(s) 00:11:00
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Predicting regiochemical and stereochemical outcomes 00:16:00
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Introduction to addition reactions 00:01:00
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Regiochemistry 00:05:00
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Stereochemistry 00:18:00
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Hydrohalogenation: adding hydrogen halide, H-X 00:09:00
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Hydrobromination : adding H-Br 00:09:00
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Hydration: adding H-OH 00:12:00
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Adding Br and Br 00:05:00
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Halohydrin formation: adding Br and OH 00:08:00
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“Anti” dihydroxylation: adding OH and OH 00:07:00
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“Anti” dihydroxylation: adding OH and OH 00:07:00
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“syn” dihydroxylation : adding OH and OH 00:04:00
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Ozonolysis 00:03:00
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Reactions summary 00:01:00
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One-step synthesis 00:03:00
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Combining reactions: changing the position of a leaving group 00:03:00
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Combining reactions: changing the position of a double bond 00:02:00
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Combining reactions: introducing functionality 00:03:00
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Thank you for enrolling and announcing part 2 00:01:00
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Assignment -Organic Chemistry Demystified 00:00:00
Frequently Bought Together
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£19.99
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This course includes:
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Duration:12 hours, 28 minutes
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Access:1 year access
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Units:82
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Level:
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CPD Points:10
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Certificate:Yes
