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.
In this lecture we continue to look at alkene reactivity with the hydroboration reaction. This reaction uses borane with an alkene followed by hydrogen peroxide oxidation in basic environment. The results are an anti-Markovinkov addition with syn stereochemistry every time.
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In this lesson we take a look at terminal alkynes and why they are mildly acidic. Hybridization and percent s character help us understand why these compounds can be acidic under some conditions.
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This lecture examines the process we must follow to determine the theoretical yield of a reaction by identifying the limiting reactant.
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The fourth lecture of the IUPAC naming series. In this lesson we learn the second rule of IUPAC naming which is how to number the main parent carbon chain in order to prioritize substituents.
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The Ideal Gas Law is discussed including its origin, how the gas law constant is determined, and practice problems.
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The Nitration of Benzene Mechanism - Electrophilic Aromatic Substitution
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A lecture examining the way organic alcohol groups tend to fragment when exposed to mass spectroscopy ionization.
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The tenth and final lecture of the IUPAC naming series. Here we practice naming alkanes with substituents putting together all we have learned.
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This lecture examines the halogenation of alkenes to alkyl halides using Br2 and Cl2 as reagents. The dihalide addition to alkenes involves a 3-membered intermediate ring with a bromine or chlorine. The resulting stereochemistry will always be anti.
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