In this lesson we learn the steps of solving for an unknown compound when presented with several spectra including mass spectroscopy, IR, proton NMR, and carbon 13 NMR.
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https://www.youtube.com/watch?v=DnntozJfUhw
This lecture takes a detailed look at acidity relative to pH as we examine the pH scale and learn how to relate the proton concentration in a solution to the pH of that solution.
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https://www.youtube.com/watch?v=TL80yfxdZSA
This lecture covers limiting reactants, theoretical yields, and percent yields. This is a very important lecture and will play a role in organic chemistry reactions down the road.
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https://www.youtube.com/watch?v=aOofO2-51DE
We examine nomenclature and naming of alkanes and cycloalkane groups by proper IUPAC standards.
Updated! Watch the complete alkane naming course here:
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https://www.youtube.com/watch?v=dNxS5Unl6q4
This lesson introduces the carboxylic acid derivatives including acid chlorides (halides), anhydrides, esters, and amides. We look at the reactivity of each derivative and explain the reasoning behind this activity.
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https://www.youtube.com/watch?v=n-qr7LIKPB8
This lesson looks at the first of 3 ways to add water to an alkene. Hydration through an acidic medium with water leads to Markovnikov addition of alcohols to alkenes. We examine the mechanism in detail.
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https://www.youtube.com/watch?v=p8xdiYDamDg
This lesson teaches how to distinguish between SN2 and SN2 reactions. Nucleophilic substitution reactions can be told apart by (1) position of leaving group (2) the type of nucleophile and (3) the solvent utilized. Stereochemical outcomes can also be utilized.
The Substitution Reaction Playlist: https://www.youtube.com/watch?v=V8y8Y09S4ck&list=PLpqnaa47Nj3ABPM8ScpLF3vwxfXNNwvMs
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https://www.youtube.com/watch?v=WkTAqFLbwS4
The ninth and final lecture of the solving unknown structure series. In this lesson we finally put all we have learned in the course together and solve an unknown structure using spectroscopy!
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The final part of the SN2 reaction series. We wrap up looking at solvent effects and how they cripple the energy of a good nucleophile when polar protic and why SN2 prefers polar aprotic. We finish discussing the section with inversion of stereochemistry.
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https://www.youtube.com/watch?v=JJZTOrJOTRI