Develop a comprehensive understanding of Organic Chemistry with this Organic chemistry demystified : 12H course + solved problems course. This course provides you with a simplified way of learning Organic Chemistry.
The Organic chemistry demystified : 12H course + solved problems training covers numerous solved problems to deepen your knowledge of Organic Chemistry fundamentals. It will provide you with step-by-step instructions on how to draw organic molecules and resonance structures. You will explore the nomenclature of Organic Chemistry and understand the concept of acid-base reactions in Organic Chemistry. In addition, you will identify what mechanisms are there in Organic Chemistry and gain the skills to solve various organic reactions.
Enroll right now and take steps to pursue a rewarding career in the field of Chemistry.
- Be able to read and draw bond-line drawings
- Learn how to draw resonance structures
- Gain in-depth knowledge of the
- Deepen your understanding of acid-base reactions
- Learn the fundamentals of resonance
- Identify the impact of resonance on geometry
- Understand the nomenclature of Organic compounds
- Learn about the various types of Organic reactions
Who Is This Course For?
This Organic chemistry demystified: 12H course + solved problems course helps aspiring professionals get started with Organic Chemistry by practicing various problems. Gaining the in-demand skills from this course offers excellent opportunities to pursue a rewarding career in the field of Chemistry.
- This course is available to all learners of all academic backgrounds.
- Learners should be aged 16 or over.
- Good understanding of English language, numeracy and ICT skills are required to take this course.
- After you have successfully completed the course, you will obtain an Accredited Certificate of Achievement. And, you will also receive a Course Completion Certificate following the course completion without sitting for the test. Certificates can be obtained either in hardcopy for £39 or in PDF format at the cost of £24.
- PDF certificate’s turnaround time is 24 hours, and for the hardcopy certificate, it is 3-9 working days.
Why Choose Us?
- Affordable, engaging & high-quality e-learning study materials;
- Tutorial videos and materials from the industry-leading experts;
- Study in a user-friendly, advanced online learning platform;
- Efficient exam systems for the assessment and instant result;
- United Kingdom & internationally recognized accredited qualification;
- Access to course content on mobile, tablet and desktop from anywhere, anytime;
- Substantial career advancement opportunities;
- 24/7 student support via email.
The Organic chemistry demystified : 12H course + solved problems training provides essential skills that will make you more effective in your role. It would be beneficial for any related profession in the industry, such as:
- Synthetic Organic Chemist
- Group Leader-Organic Chemistry
|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|
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