2521 Courses in Leicester delivered Online

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 • 12:28:00 total length •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 •Orbitals: 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 •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 •'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: changing the position of a double bond: 00:02:00 •Combining reactions: introducing functionality: 00:03:00 •Thank you for enrolling and announcing part 2: 00:01:00 •Assignment -Organic Chemistry Demystified: 00:00:00

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