Description

Organic Chemistry is yet another 'Teacher's Choice' course from Teachers Training for a complete understanding of the fundamental topics. You are also entitled to exclusive tutor support and a professional CPD-accredited certificate in addition to the special discounted price for a limited time. Just like all our courses, this Organic Chemistry and its curriculum have also been designed by expert teachers so that teachers of tomorrow can learn from the best and equip themselves with all the necessary skills.

Consisting of several modules, the course teaches you everything you need to succeed in this profession.

The course can be studied part-time. You can become accredited within 12 hours studying at your own pace. Your qualification will be recognised and can be checked for validity on our dedicated website.

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No formal entry requirements. You need to have:

Passion for learning

A good understanding of the English language

Be motivated and hard-working

Over the age of 16.

Certification

Successfully completing the MCQ exam of this course qualifies you for a CPD-accredited certificate from The Teachers Training. You will be eligible for both PDF copy and hard copy of the certificate to showcase your achievement however you wish.

You can get your digital certificate (PDF) for £4.99 only

Hard copy certificates are also available, and you can get one for only £10.99

You can get both PDF and Hard copy certificates for just £12.99!

The certificate will add significant weight to your CV and will give you a competitive advantage when applying for jobs.

Unit 01: About the Course
	Introduction	00:02:00
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
	Recognizing patterns	00:30:00
	The relative importance of resonance structures	00:19:00
Unit 04: Acid-Base Reactions
	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
Unit 05: Geometry
	Orbitals	00:15:00
	Goemetry of orbitals	00:15:00
	Impact of resonance on geometry	00:01:00
Unit 06: Nomenclature
	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
Unit 07: Conformations
	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
Unit 08: Configurations
	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
Unit 09: Mechanisms
	Introduction to mechanisms	00:02:00
	Nucleophiles and electrophiles	00:09:00
	Arrows used for mechanisms	00:14:00
	Carbocation	00:15:00
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
	E1 mechanism	00:08:00
	E2 mechanism	00:20:00
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
	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
Unit 14: Synthesis Techniques
	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
Unit 15: Wrapping Up and Bonus
	Thank you for enrolling and announcing part 2	00:01:00

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Organic Chemistry

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