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\nE1 and E2 Reactions - Crash Course Organic Chemistry \n

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\n\nPublisher:\n\nCrash Course\n\n\n
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\nWe’ve spent the last few episodes talking about substitution reactions, but now it’s time to talk about a related type of reaction: elimination reactions! Elimination reactions are super important because they are the main way we can...\nWe’ve spent the last few episodes talking about substitution reactions, but now it’s time to talk about a related type of reaction: elimination reactions! Elimination reactions are super important because they are the main way we can make compounds with double and triple bonds in organic chemistry. In this episode of Crash Course Organic Chemistry we’re going to cover… a lot, including a review of substitution reactions, E1 and E2 mechanisms, Zaitsev’s rule, and more. And of course, we’ll finish with some practice problems.\n
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Resource Details

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Curator Rating
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Educator Rating
Not yet Rated
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Media Length
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13:30
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Grade
12th - Higher Ed
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Subjects
Science
5 more...
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Media Type
Instructional Videos
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Source:
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\nCrash Course Organic Chemistry\n\n
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Date
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2021
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Language
English
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Audiences
For Teacher Use
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Usage Permissions
Fine Print: Educational Use
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Concepts

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data, organic chemistry, education
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Additional Tags

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nucleophile acts, beta carbon, phosphoric acid, π bond, e2 reaction, carbo cation, strong base, hydrogen atom, chemical reaction, minor product, elimination reaction, opposite sides, nucleophile attacks, sulfuric acid, newman projection, e1 reaction, double bond, leaving group, beta proton, alpha carbon, electron donor, methyl groups, substitution reactions, crashcourse, experiments, good nucleophile, science, major product, e2 mechanism, chair confirmation, chemistry, beta hydrogen, proton acceptor
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Classroom Considerations

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Best For: Explaining a topic
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