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Organic Chemistry Midterm Practice: Step-by-Step Guidance
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Lewis Structure
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Drawing the Lewis Structure for N2H4.
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How to use Organic Chemistry to make Lewis Structures easier.
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Naming Cycloalkanes
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00:53
Name the following alkane
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00:18
Determining Root Name
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00:34
Determining Root Name
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Naming Alkyl Halides
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01:52
How to name alkyl halides
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01:58
Name the following alkyl halide
Johnny Betancourt
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03:53
Name the following alkyl halide
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Hybridization
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How carbon creates 4 partially-filled orbitals.
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04:58
Bond sites, hybridization, and intermediate orbitals
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02:47
Introduction to the reactive intermediates.
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Molecular Geometry
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Predict the hybridization and molecular geometry
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07:44
Molecular Geometry Explained.
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Intermolecular Forces
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01:46
How dipole-dipole forces work.
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03:08
How IMFs are related to melting and boiling points.
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03:01
How Van der Waals forces work.
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Solubility
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Introducing common solvents and other molecules in organic chemistry.
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Understanding “like dissolves like”.
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Chirality
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03:24
Drawing Mirror Images and Determining Chirality
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05:10
What is chirality?
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Drawing Mirror Images and Determining Chirality
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Cahn-Ingold-Prelog Nomenclature
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R and S Naming- Step 4
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01:48
Why stereoisomers need their own naming system.
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Determining Priorities
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Fischer Projection
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Introduction to different projections.
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05:45
How to convert Fischer projections into bondline structures
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03:38
Convert the following Fischer projection into bondline structure.
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Fischer Configurations
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02:32
R and S rule for Fischer Projections.
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05:25
Determining Absolute Configurations
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Types of Isomers
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01:39
Determining when molecules are conformers.
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Determining when molecules are different.
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Determining when molecules are constitutional isomers.
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Cis vs Trans
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Why we need to use the E/Z naming system
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00:50
What does E and Z stand for?
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How to name different types of double bonds or rings
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