Balancing Chemical Equations and Using Stoichiometric Coefficients
This lesson teaches balancing chemical equations in a step by step process. Learn how to properly utilize stoichiometric coefficients. ... https://www.youtube.com/watch?v=-EEVRBXKQyk
In this lecture we study the IUPAC method of naming carboxylic acids and how to handle both open chain and cyclic systems with carboxylic acids present.
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In this video we continue to examine NMR spectra as we discuss the concept of shielding and deshielding of nuclei. Chemical shift predictions in ppm come from this concept.
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https://www.youtube.com/watch?v=P5MuaeaqOnE
This lecture examines the addition of acid halides to alkene functional groups. A detailed examination of electron density, electronegativity and carbocation stability allows us to study the reaction and its mechanism in detail.
Hyperconjugation Lecture: https://www.youtube.com/watch?v=ZRp4F6ktSB0
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https://www.youtube.com/watch?v=qMacsPylxag
We take a look at SN1 reactions including the presence of carbocation intermediates, leaving group ranks, and the need for a milder and weaker neutral nucleophile.
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https://www.youtube.com/watch?v=ckx9J1fHsA4
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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https://www.youtube.com/watch?v=m36kC04_Y80
In this lesson we further examine NMR and the concept of integration which leads to hydrogen ratio of each signal.
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https://www.youtube.com/watch?v=qKZizWnEPfw
In this lecture we examine the even and odd "nitrogen rule" in relation to compound mass when dealing with organic compounds. This rule if very useful when identifying compounds using mass spec.
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In this lecture we examine the important role carbocations play in predicting the potential number of stereoisomer products. The trigonal planar and flat nature of these intermediates often lead to attack from both sides with a potential to produce multiple products in the presence of chirality.
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Our first glance into SN2 reactions. SN2 are bimolecular reactions meaning they rely on both the leaving group and nucleophile to cooperate at the same time. We also look at leaving group position.
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https://www.youtube.com/watch?v=V8y8Y09S4ck