This lesson discusses how to figure out if lone pairs of electrons are in hybrid orbitals or p-orbitals. This relates heavily to resonance and aromaticity lectures.
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https://www.youtube.com/watch?v=vyuh0ykJUEw
This lesson examines the formation of acetal and ketal groups using aldehydes and ketones with various alcohols under acidic reversible conditions.
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https://www.youtube.com/watch?v=aYjnY0_UcYM
This lecture discusses the criteria for a compound to meet the classification of aromatic and how to apply Huckel's Rule.
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https://www.youtube.com/watch?v=9yXXfYtZui4
A multipart series discussing the hybridization of carbon in all of the various hybrid states including sp3, sp2 and sp. A detailed look at non carbon based atoms helps us determine how to handle lone pairs and the hybridization states of oxygen, nitrogen and the halogens.
Hybridization Playlist:
https://www.youtube.com/watch?v=99qY8RqwE38&list=PLpqnaa47Nj3CclEQwyn2AgJv-qoLc5aRm
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This lesson reviews previous organic synthesis techniques for creating alcohols in Organic Chemistry I. Please see those individual reaction videos for details. Recap of alkene hydration, alkene diol formation, and SN2 alcohol formation.
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https://www.youtube.com/watch?v=QqZ-SZwtx7A
Significant Figures Lecture and Explanation for chemistry class. We discuss what a significant figure is, the certainty of measurements, rules for determining a significant figure, and how to predict the significant figures when answering a mathematical calculation.
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https://www.youtube.com/watch?v=MyCY_OBfM7s
We examine nomenclature and naming of alkanes and cycloalkane groups by proper IUPAC standards.
Updated! Watch the complete alkane naming course here:
https://www.youtube.com/watch?v=BEh8I15ZEAo&list=PLpqnaa47Nj3D6K4VcHTG4TbZur2K15DY7
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https://www.youtube.com/watch?v=dNxS5Unl6q4
This lecture examines the role of hydrogen bonding and how it can affect the chemical shift (ppm) in NMR spectroscopy.
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A lecture series discussing enolate chemistry. This lesson begins to examine the process of the aldol condensation. We start with simple self aldol condensation products that dehydrate to create conjugated enones.
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