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CPD Accredited & QLS Endorsed Course

  • (5)
  • Calendar 4 Students
  • Calendar 1 Year
  • calendar Intermediate
  • clock 12 hours, 26 minutes

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Course Overview

Organic Chemistry Demystified is a comprehensive course designed to unravel the complexities of organic chemistry. This course delves into the fundamental concepts and reactions that form the backbone of organic chemistry, making it accessible and engaging for students. Whether you're a beginner or have some prior knowledge, this course breaks down intricate topics into digestible segments, providing clear explanations and practical examples. By the end of the course, you'll gain a strong foundation in organic chemistry, enabling you to tackle more advanced topics with confidence. This course is perfect for students, professionals, and enthusiasts who wish to deepen their understanding of organic chemistry. With a focus on clarity and simplicity, Organic Chemistry Demystified makes learning this essential subject enjoyable and rewarding.

Brace yourself, and enrol now for an amazing venture!

This Organic Chemistry Demystified Course Package Includes

  • Free CPD Accredited PDF Certificate
  • Comprehensive lessons and training provided by experts on Diploma in Organic Chemistry Demystified
  • Interactive online learning experience provided by qualified professionals at your convenience
  • 24/7 Access to the course materials and learner assistance
  • Easy accessibility from any smart device (Laptop, Tablet, Smartphone etc.)
  • A happy and handy learning experience for the professionals and students
  • 100% learning satisfaction, guaranteed by Compliance Central — a leading compliance training provider approved by IAO

Learning Outcome

Upon successful completion of this highly appreciated Organic Chemistry Demystified course, you’ll be a skilled professional. Besides—
  • Understand the basic principles of organic chemistry.
  • Identify and classify organic compounds and functional groups.
  • Predict the outcomes of common organic reactions.
  • Master the mechanisms of key organic reactions.
  • Apply organic chemistry concepts to real-world problems.
  • Interpret and analyze organic chemistry data.
  • Develop problem-solving skills specific to organic chemistry.
  • Build a solid foundation for advanced study in chemistry.

Assessment

Complete this Organic Chemistry Demystified course and sit for a short online assessment to instantly evaluate your understanding of the subject. The test will be automated, and your answers will be checked and reviewed then and there. You'll also get unlimited chances to retake the exam! Our concern is to make you competent for the job, so we will fully support your learning and understanding of it thoroughly. The test fees are included in the one-time paid course fee. As said earlier, you can retake the exam if you fail early—you will not be charged any money for later attempts.  

Certificate of Achievement

CPD Accredited Certificate
CPD-accredited certificates are available for £4.79 (instant PDF download) or £10.79 (hard copy delivered to you). Our courses are regularly reviewed to ensure they are up-to-date. Certificates do not expire, but reviewing or renewing them annually is recommended.

Who Is This Course For

Compliance Central aims to prepare efficient human resources for the industry and make it more productive than ever. This helpful course is suitable for any person who is interested in a Organic Chemistry Demystified. There are no pre-requirements to take it. You can attend the course if you are a student, an enthusiast or a
  • Students preparing for chemistry exams.
  • Professionals looking to refresh their knowledge of organic chemistry.
  • Individuals interested in pursuing a career in chemistry or related fields.
  • Educators seeking additional resources for teaching organic chemistry.
  • Laboratory technicians aiming to enhance their understanding of organic reactions.
  • Science enthusiasts curious about the principles of organic chemistry.
  • Pre-med students requiring a solid foundation in organic chemistry.
  • Chemical engineers needing to reinforce their organic chemistry skills.
  • Biochemists looking to deepen their knowledge of organic molecules.
  • Anyone interested in demystifying the complexities of organic chemistry.

Course Currilcum

    • Introduction 00:02:00
    • 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
    • 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
    • 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
    • Orbitals14 00:15:00
    • Goemetry of orbitals 00:15:00
    • Impact of resonance on geometry 00:01:00
    • 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
    • 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
    • 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
    • Introduction to mechanisms 00:02:00
    • Nucleophiles and electrophiles 00:09:00
    • Arrows used for mechanisms 00:14:00
    • Carbocation 00:15:00
    • 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
    • Introduction to elimination reactions 00:02:00
    • E1 mechanism 00:08:00
    • E2 mechanism 00:20:00
    • 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
    • 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
    • One-step synthesis 00:03:00
    • Combining reactions: changing the position of a leaving group 00:03:00
    • Combining reactions: introducing functionality 00:03:00
    • Thank you for enrolling and announcing part 2 00:01:00
    • Order Your CPD Certificate 00:00:00

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Student Reviews

Ben lim

Gaining improve knowledge in the construction project management and the course is easy to understand.

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Very good and informative and quick with marking my assignments and issuing my certificate.

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The first aid course was very informative with well organised curriculum. I already have some bit and pieces knowledge of first aid, this course helped me a lot.

Ben lim

Gaining improve knowledge in the construction project management and the course is easy to understand.

Thelma Gittens

Highly recommended. The module is easy to understand and definitely the best value for money. Many thanks

BF Carey

First course with Compliance Central. It was a good experience.

Course Currilcum

    • Introduction 00:02:00
    • 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
    • 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
    • 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
    • Orbitals14 00:15:00
    • Goemetry of orbitals 00:15:00
    • Impact of resonance on geometry 00:01:00
    • 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
    • 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
    • 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
    • Introduction to mechanisms 00:02:00
    • Nucleophiles and electrophiles 00:09:00
    • Arrows used for mechanisms 00:14:00
    • Carbocation 00:15:00
    • 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
    • Introduction to elimination reactions 00:02:00
    • E1 mechanism 00:08:00
    • E2 mechanism 00:20:00
    • 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
    • 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
    • One-step synthesis 00:03:00
    • Combining reactions: changing the position of a leaving group 00:03:00
    • Combining reactions: introducing functionality 00:03:00
    • Thank you for enrolling and announcing part 2 00:01:00
    • Order Your CPD Certificate 00:00:00