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Redaktion Chemie:

Sander HannesYasemin GökkuşDarja Bücker
Themenseite im Fachportal Chemie

Reaktionsmechanismen

Reaktionsmechanismen sind ein wichtiges Hilfsmittel der organischen Chemie - und gleichzeitig wichtiger Forschungsgegenstand. Der Mechanismus einer chemischen Reaktion gibt Auskunft über den exakten Ablauf der Teilschritte der Reaktion. Reaktionsmechanismen sind daher ein wichtiges Hilfsmittel, um chemische Reaktionen zu verstehen, zu steuern und zu optimieren. Es existiert eine gewissen Korrespondenz von Reaktionsmechanismus und Stoffklasse: Bestimmte Stoffklassen reagieren meist bevorzugt nach einem typischen Reaktionsmechanismus.

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Cover: Alkenes & Alkynes: Crash Course Chemistry #41
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Video (9 Minuten)

Today Hank talks about the deliciousness of alkenes & alkynes, their structures, and how to remember which is which by simply knowing the alphabet. Also, he breaks down hydrogenation, halogenation, polymerization, and triglycerides all while helping us figure out the meaning of different names for fats. Pssst... we made flashcards to help you review the content in this episode! Find them on the free Crash Course App! Download it here for Apple Devices: https://apple.co/3d4eyZo Download it here for Android Devices: https://bit.ly/2SrDulJ -- Table of Contents Alkenes & Alkynes 1:14 Naming Rules 1:39 Cis-Trans Isomerism 3:29 Hydrogenation, Halogenation, Polymerization, and Triglycerides 4:40 Meanings of Fat Names 5:50 -- Crash Course is on Patreon! You can support us directly by signing up at http://www.patreon.com/crashcourse Want to find Crash Course elsewhere on the internet? Facebook - http://www.facebook.com/YouTubeCrashCourse Twitter - http://www.twitter.com/TheCrashCourse Instagram - https://www.instagram.com/thecrashcourse/ CC Kids: http://www.youtube.com/crashcoursekids

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Allgemein: Sekundarstufe II, Hochschule

Youtube

Cover: E/Z Alkenes, Electrophilic Addition, & Carbocations: Crash Course Organic Chemistry #14
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Video (14 Minuten)

Alkenes are an important type of molecule in organic chemistry that we’re going to see a lot more of in this series. But before we can really get into the many cool reactions alkenes do, we need to go over some of the basics. In this episode of Crash Course Organic Chemistry, we’ll review and build on our knowledge of alkene nomenclature, revisit our friend the carbocation, and learn Markovnikov’s Rule: an important tool that will help us predict the products of addition reactions involving alkenes. Series Sources: Brown, W. H., Iverson, B. L., Ansyln, E. V., Foote, C., Organic Chemistry; 8th ed.; Cengage Learning, Boston, 2018. Bruice, P. Y., Organic Chemistry, 7th ed.; Pearson Education, Inc., United States, 2014. Clayden, J., Greeves, N., Warren., S., Organic Chemistry, 2nd ed.; Oxford University Press, New York, 2012. Jones Jr., M.; Fleming, S. A., Organic Chemistry, 5th ed.; W. W. Norton & Company, New York, 2014. Klein., D., Organic Chemistry; 1st ed.; John Wiley & Sons, United States, 2012. Louden M., Organic Chemistry; 5th ed.; Roberts and Company Publishers, Colorado, 2009. McMurry, J., Organic Chemistry, 9th ed.; Cengage Learning, Boston, 2016. Smith, J. G., Organic chemistry; 6th ed.; McGraw-Hill Education, New York, 2020. Wade., L. G., Organic Chemistry; 8th ed.; Pearson Education, Inc., United States, 2013. *** Watch our videos and review your learning with the Crash Course App! Download here for Apple Devices: https://apple.co/3d4eyZo Download here for Android Devices: https://bit.ly/2SrDulJ Crash Course is on Patreon! You can support us directly by signing up at http://www.patreon.com/crashcourse Thanks to the following patrons for their generous monthly contributions that help keep Crash Course free for everyone forever: Catherine Conroy, Patty Laqua, Leonora Rossé Muñoz, Stephen Saar, John Lee, Phil Simmons, Alexander Thomson, Mark & Susan Billian, Junrong Eric Zhu, Alan Bridgeman, Jennifer Smith, Matt Curls, Tim Kwist, Ron Lin, Jonathan Zbikowski. Jennifer Killen, Sarah & Nathan Catchings, Brandon Westmoreland, team dorsey, Trevin Beattie, Eric Prestemon, Sam Ferguson, Yasenia Cruz, Eric Koslow, Indika Siriwardena, Khaled El Shalakany, Shawn Arnold, Tom Trval, Siobhán, Ken Penttinen, Nathan Taylor, William McGraw, Justin Zingsheim, Andrei Krishkevich, Jirat, Brian Thomas Gossett, SR Foxley, Ian Dundore, Jason A Saslow, Jessica Wode, Mark, Caleb Weeks, Sam Buck -- Want to find Crash Course elsewhere on the internet? Facebook - http://www.facebook.com/YouTubeCrashCourse Twitter - http://www.twitter.com/TheCrashCourse Tumblr - http://thecrashcourse.tumblr.com Support Crash Course on Patreon: http://patreon.com/crashcourse CC Kids: http://www.youtube.com/crashcoursekids

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Biologie, Chemie: Sekundarstufe II, Hochschule

Youtube

Cover: Alkene Addition Reactions: Crash Course Organic Chemistry #16
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Video (12 Minuten)

Like a trendy dance, a fighting combo, or a secret handshake, organic reactions can be broken down into simpler steps. In this episode of Crash Course Organic Chemistry, we’ll specifically be looking at alkene addition reactions, and with each new reaction ask ourselves three questions to help us puzzle through the mechanism and understand what’s going on. Episode Sources: Le Couteur, P, Burreson, J. Napoleon’s Buttons: 17 molecules that changed history., Penguin, New York, 2004, Chapter 1. Whipps, H., “How the Spice Trade Changed the World,” https://www.livescience.com/7495-spice-trade-changed-world.html Last accessed, 3/28/2020. Henriques, Martha, “How spices changed the ancient world,” http://www.bbc.com/future/bespoke/made-on-earth/the-flavours-that-shaped-the-world/ Last accessed, 3/28/2020. Hashimoto, K., Yaoi, T., Koshiba, H., Yoshida, T., Maoka, T., Fujiwara, Y., Yaamoto, Y, Mori, K., “Photochemical Isomerization of Piperine, a Pungent Constituent of Pepper”, Food Sci. Technol., Int. 1996, 2 (1), 24-29. Series Sources: Brown, W. H., Iverson, B. L., Ansyln, E. V., Foote, C., Organic Chemistry; 8th ed.; Cengage Learning, Boston, 2018. Bruice, P. Y., Organic Chemistry, 7th ed.; Pearson Education, Inc., United States, 2014. Clayden, J., Greeves, N., Warren., S., Organic Chemistry, 2nd ed.; Oxford University Press, New York, 2012. Jones Jr., M.; Fleming, S. A., Organic Chemistry, 5th ed.; W. W. Norton & Company, New York, 2014. Klein., D., Organic Chemistry; 1st ed.; John Wiley & Sons, United States, 2012. Louden M., Organic Chemistry; 5th ed.; Roberts and Company Publishers, Colorado, 2009. McMurry, J., Organic Chemistry, 9th ed.; Cengage Learning, Boston, 2016. Smith, J. G., Organic chemistry; 6th ed.; McGraw-Hill Education, New York, 2020. Wade., L. G., Organic Chemistry; 8th ed.; Pearson Education, Inc., United States, 2013. *** Watch our videos and review your learning with the Crash Course App! Download here for Apple Devices: https://apple.co/3d4eyZo Download here for Android Devices: https://bit.ly/2SrDulJ Crash Course is on Patreon! You can support us directly by signing up at http://www.patreon.com/crashcourse Thanks to the following patrons for their generous monthly contributions that help keep Crash Course free for everyone forever: Vincent LaBarca, Bjartur Thorlacius, Scott Harrison, Alexander Thomson, Mark & Susan Billian, Junrong Eric Zhu, Alan Bridgeman, Jennifer Smith, Matt Curls, Tim Kwist, Jonathan Zbikowski, Jennifer Killen, Sarah & Nathan Catchings, Brandon Westmoreland, team dorsey, Trevin Beattie, Yasenia Cruz, Eric Koslow, Indika Siriwardena, Khaled El Shalakany, Shawn Arnold, Siobhán, Ken Penttinen, Nathan Taylor, William McGraw, Andrei Krishkevich, Sam Ferguson, Jirat, Brian Thomas Gossett, SR Foxley, Ian Dundore, Jason A Saslow, Jessica Wode, Caleb Weeks, Mark, Patty Laqua, Stephen Saar, John Lee, Eric Prestemon __ Want to find Crash Course elsewhere on the internet? Facebook - http://www.facebook.com/YouTubeCrashCourse Twitter - http://www.twitter.com/TheCrashCourse Tumblr - http://thecrashcourse.tumblr.com Support Crash Course on Patreon: http://patreon.com/crashcourse CC Kids: http://www.youtube.com/crashcoursekids

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Biologie, Chemie: Sekundarstufe II, Hochschule

Youtube

Cover: Alkyne Reactions & Tautomerization: Crash Course Organic Chemistry #18
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Video (11 Minuten)

Carbon-carbon double bonds are pretty common in nature, but triple bonds between carbons, called alkynes, are not. When alkynes do pop up in nature, it’s usually in a compound that’s toxic to humans, however, we can synthesize alkynes that are life saving medicines and materials. In this episode of Crash Course Organic Chemistry, we’ll learn about alkynes and some of the reactions we can use them in (hint: it’s a lot of the same reactions we used for alkenes!) Series Sources: Brown, W. H., Iverson, B. L., Ansyln, E. V., Foote, C., Organic Chemistry; 8th ed.; Cengage Learning, Boston, 2018. Bruice, P. Y., Organic Chemistry, 7th ed.; Pearson Education, Inc., United States, 2014. Clayden, J., Greeves, N., Warren., S., Organic Chemistry, 2nd ed.; Oxford University Press, New York, 2012. Jones Jr., M.; Fleming, S. A., Organic Chemistry, 5th ed.; W. W. Norton & Company, New York, 2014. Klein., D., Organic Chemistry; 1st ed.; John Wiley & Sons, United States, 2012. Louden M., Organic Chemistry; 5th ed.; Roberts and Company Publishers, Colorado, 2009. McMurry, J., Organic Chemistry, 9th ed.; Cengage Learning, Boston, 2016. Smith, J. G., Organic chemistry; 6th ed.; McGraw-Hill Education, New York, 2020. Wade., L. G., Organic Chemistry; 8th ed.; Pearson Education, Inc., United States, 2013. *** Watch our videos and review your learning with the Crash Course App! Download here for Apple Devices: https://apple.co/3d4eyZo Download here for Android Devices: https://bit.ly/2SrDulJ Crash Course is on Patreon! You can support us directly by signing up at http://www.patreon.com/crashcourse Thanks to the following patrons for their generous monthly contributions that help keep Crash Course free for everyone forever: Eric Prestemon, Mark, DAVID MORTON HUDSON, Perry Joyce, Isaac Liu, Scott Harrison, Mark & Susan Billian, Junrong Eric Zhu, Alan Bridgeman, Jennifer Smith, Matt Curls, Tim Kwist, Jonathan Zbikowski, Jennifer Killen, Sarah & Nathan Catchings, Brandon Westmoreland, team dorsey, Trevin Beattie, Eric Koslow, Indika Siriwardena, Khaled El Shalakany, Shawn Arnold, Siobhán, Ken Penttinen, Nathan Taylor, William McGraw, Jirat, Brian Thomas Gossett, Ian Dundore, Jason A Saslow, Jessica Wode, Caleb Weeks __ Want to find Crash Course elsewhere on the internet? Facebook - http://www.facebook.com/YouTubeCrashCourse Twitter - http://www.twitter.com/TheCrashCourse Tumblr - http://thecrashcourse.tumblr.com Support Crash Course on Patreon: http://patreon.com/crashcourse CC Kids: http://www.youtube.com/crashcoursekids

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Biologie, Chemie: Sekundarstufe II, Hochschule

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Cover: Radical Reactions & Hammond's Postulate: Crash Course Organic Chemistry #19
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Video (12 Minuten)

Throughout this series we’ve mostly talked about pairs of electrons, but electrons don’t always have a buddy. An atom or group of atoms with a single unpaired electron is called a radical. In this episode of Crash Course Organic Chemistry, we’ll learn all about radicals including the three key steps in a radical reaction and Hammond’s Postulate, an important tool to help us understand these reactions. We’ll also see ways radicals can react with alkanes, alkenes, and alkynes. Episode Sources: Davies, K. J., & Doroshow, J. H. (1986). Redox cycling of anthracyclines by cardiac mitochondria. I. Anthracycline radical formation by NADH dehydrogenase. Journal of Biological Chemistry, 261(7), 3060-3067. Ball, P. (Interview with Nick Lane) Yes, life in the fast lane kills you. May 5, 2016. Bond Dissociation Energies https://chem.libretexts.org/Bookshelves/Physical_and_Theoretical_Chemistry_Textbook_Maps/Supplemental_Modules_(Physical_and_Theoretical_Chemistry)/Chemical_Bonding/Fundamentals_of_Chemical_Bonding/Bond_Energies Nimse, S. B., & Pal, D. (2015). Free radicals, natural antioxidants, and their reaction mechanisms. Rsc Advances, 5(35), 27986-28006. Santos-Sánchez, N. F., Salas-Coronado, R., Villanueva-Cañongo, C., & Hernández-Carlos, B. (2019). Antioxidant compounds and their antioxidant mechanism. In Antioxidants. IntechOpen. Review of Vitamin C https://www.sciencedirect.com/topics/chemistry/vitamin-c Series Sources: Brown, W. H., Iverson, B. L., Ansyln, E. V., Foote, C., Organic Chemistry; 8th ed.; Cengage Learning, Boston, 2018. Bruice, P. Y., Organic Chemistry, 7th ed.; Pearson Education, Inc., United States, 2014. Clayden, J., Greeves, N., Warren., S., Organic Chemistry, 2nd ed.; Oxford University Press, New York, 2012. Jones Jr., M.; Fleming, S. A., Organic Chemistry, 5th ed.; W. W. Norton & Company, New York, 2014. Klein., D., Organic Chemistry; 1st ed.; John Wiley & Sons, United States, 2012. Louden M., Organic Chemistry; 5th ed.; Roberts and Company Publishers, Colorado, 2009. McMurry, J., Organic Chemistry, 9th ed.; Cengage Learning, Boston, 2016. Smith, J. G., Organic chemistry; 6th ed.; McGraw-Hill Education, New York, 2020. Wade., L. G., Organic Chemistry; 8th ed.; Pearson Education, Inc., United States, 2013. *** Watch our videos and review your learning with the Crash Course App! Download here for Apple Devices: https://apple.co/3d4eyZo Download here for Android Devices: https://bit.ly/2SrDulJ Crash Course is on Patreon! You can support us directly by signing up at http://www.patreon.com/crashcourse Thanks to the following patrons for their generous monthly contributions that help keep Crash Course free for everyone forever: Eric Prestemon, Mark, DAVID MORTON HUDSON, Perry Joyce, Isaac Liu, Scott Harrison, Mark & Susan Billian, Junrong Eric Zhu, Alan Bridgeman, Jennifer Smith, Matt Curls, Tim Kwist, Jonathan Zbikowski, Jennifer Killen, Sarah & Nathan Catchings, Brandon Westmoreland, team dorsey, Trevin Beattie, Eric Koslow, Indika Siriwardena, Khaled El Shalakany, Shawn Arnold, Siobhán, Ken Penttinen, Nathan Taylor, William McGraw, Jirat, Brian Thomas Gossett, Ian Dundore, Jason A Saslow, Jessica Wode, Caleb Weeks __ Want to find Crash Course elsewhere on the internet? Facebook - http://www.facebook.com/YouTubeCrashCourse Twitter - http://www.twitter.com/TheCrashCourse Tumblr - http://thecrashcourse.tumblr.com Support Crash Course on Patreon: http://patreon.com/crashcourse CC Kids: http://www.youtube.com/crashcoursekids

Video

Chemie: Sekundarstufe II, Hochschule

Youtube

Cover: Intro to Substitution Reactions: Crash Course Organic Chemistry #20
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Video (12 Minuten)

Substitution reactions can have really powerful effects, both good and bad, in our bodies. You might remember substitution reactions as displacement reactions from general chemistry, but (you guessed it!) in organic chemistry they’re a bit more complicated. In this episode of Crash Course Organic Chemistry, we’ll learn about the two pathways substitution reactions can take: SN1 and SN2 mechanisms, which substrates prefer which mechanism, and we’ll apply this knowledge by looking at how substitution reactions make chemotherapy treatments work. Episode Sources: Brookes, P., Lawley, P.D. “The Reaction of Mono-and Di-Functional Alkylating Agents with Nucleic Acids,” , Biochem. J., 1961, 80, 496-503. Series Sources: Brown, W. H., Iverson, B. L., Ansyln, E. V., Foote, C., Organic Chemistry; 8th ed.; Cengage Learning, Boston, 2018. Bruice, P. Y., Organic Chemistry, 7th ed.; Pearson Education, Inc., United States, 2014. Clayden, J., Greeves, N., Warren., S., Organic Chemistry, 2nd ed.; Oxford University Press, New York, 2012. Jones Jr., M.; Fleming, S. A., Organic Chemistry, 5th ed.; W. W. Norton & Company, New York, 2014. Klein., D., Organic Chemistry; 1st ed.; John Wiley & Sons, United States, 2012. Louden M., Organic Chemistry; 5th ed.; Roberts and Company Publishers, Colorado, 2009. McMurry, J., Organic Chemistry, 9th ed.; Cengage Learning, Boston, 2016. Smith, J. G., Organic chemistry; 6th ed.; McGraw-Hill Education, New York, 2020. Wade., L. G., Organic Chemistry; 8th ed.; Pearson Education, Inc., United States, 2013. *** Watch our videos and review your learning with the Crash Course App! Download here for Apple Devices: https://apple.co/3d4eyZo Download here for Android Devices: https://bit.ly/2SrDulJ Crash Course is on Patreon! You can support us directly by signing up at http://www.patreon.com/crashcourse Thanks to the following patrons for their generous monthly contributions that help keep Crash Course free for everyone forever: Eric Prestemon, Mark, DAVID MORTON HUDSON, Perry Joyce, Isaac Liu, Scott Harrison, Mark & Susan Billian, Junrong Eric Zhu, Alan Bridgeman, Jennifer Smith, Matt Curls, Tim Kwist, Jonathan Zbikowski, Jennifer Killen, Sarah & Nathan Catchings, Brandon Westmoreland, team dorsey, Trevin Beattie, Eric Koslow, Indika Siriwardena, Khaled El Shalakany, Shawn Arnold, Siobhán, Ken Penttinen, Nathan Taylor, William McGraw, Jirat, Brian Thomas Gossett, Ian Dundore, Jason A Saslow, Jessica Wode, Caleb Weeks __ Want to find Crash Course elsewhere on the internet? Facebook - http://www.facebook.com/YouTubeCrashCourse Twitter - http://www.twitter.com/TheCrashCourse Tumblr - http://thecrashcourse.tumblr.com Support Crash Course on Patreon: http://patreon.com/crashcourse CC Kids: http://www.youtube.com/crashcoursekids

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Biologie, Chemie: Sekundarstufe II, Hochschule

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Cover: Substitution Reactions - SN1 and SN2 Mechanisms: Crash Course Organic Chemistry #21
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Video (12 Minuten)

We’ve already learned a bit about substitution reactions in organic chemistry and the two different paths they can follow: SN1 and SN2. In order to better predict the products of a substitution reaction and understand how they work, we need to be able to figure out which mechanism a reaction is likely to follow. In this episode of Crash Course Organic Chemistry, we’ll deepen our knowledge of substitution reactions by looking at factors like substrate structure and reaction conditions to determine whether SN1 or SN2 is the more likely mechanism. Episode Sources: Brookes, P., Lawley, P.D. “The Reaction of Mono-and Di-Functional Alkylating Agents with Nucleic Acids,” , Biochem. J., 1961, 80, 496-503. Copley, Shelley, D., “Microbial dehalogenases: Enzymes recruited to convert xenobiotic substrates,” Current opinion in Chemical Biology, 1998, 2, 613-617. Janssen, D. B., Scheper, A., Dijkhuizen, L, Witholt, B., “Degradation of halogenated aliphatic compounds by Xanthobacter autotrophicus GJ10,” Applied and Environmental Microbiology, 1985, 29, 673-677. Silberstein, M., Dambrosky, J., Vajda, S., “Exploring the binding sites of the haloalkane dehalogenase Dhla from Xanthobacter autotrophicus GJ10,” Biochemistry, 2007, 46,9239-9249. Brunning, Andy, “The chemistry of dry cleaning,” https://cen.acs.org/articles/95/i45/Periodic-graphics-chemistry-dry-cleaning.html McCoy, M., “Dry Cleaning Dreams,” Chemistry and Engineering News, 2005, 83(46), 19-22. Series Sources: Brown, W. H., Iverson, B. L., Ansyln, E. V., Foote, C., Organic Chemistry; 8th ed.; Cengage Learning, Boston, 2018. Bruice, P. Y., Organic Chemistry, 7th ed.; Pearson Education, Inc., United States, 2014. Clayden, J., Greeves, N., Warren., S., Organic Chemistry, 2nd ed.; Oxford University Press, New York, 2012. Jones Jr., M.; Fleming, S. A., Organic Chemistry, 5th ed.; W. W. Norton & Company, New York, 2014. Klein., D., Organic Chemistry; 1st ed.; John Wiley & Sons, United States, 2012. Louden M., Organic Chemistry; 5th ed.; Roberts and Company Publishers, Colorado, 2009. McMurry, J., Organic Chemistry, 9th ed.; Cengage Learning, Boston, 2016. Smith, J. G., Organic chemistry; 6th ed.; McGraw-Hill Education, New York, 2020. Wade., L. G., Organic Chemistry; 8th ed.; Pearson Education, Inc., United States, 2013. *** Watch our videos and review your learning with the Crash Course App! Download here for Apple Devices: https://apple.co/3d4eyZo Download here for Android Devices: https://bit.ly/2SrDulJ Crash Course is on Patreon! You can support us directly by signing up at http://www.patreon.com/crashcourse Thanks to the following patrons for their generous monthly contributions that help keep Crash Course free for everyone forever: Christine Phelan, Nick, DAVID MORTON HUDSON, Perry Joyce, Scott Harrison, Mark & Susan Billian, Junrong Eric Zhu, Alan Bridgeman, Jennifer Smith, Matt Curls, Tim Kwist, Jonathan Zbikowski, Jennifer Killen, Sarah & Nathan Catchings, Brandon Westmoreland, team dorsey, Trevin Beattie, Eric Koslow, Indika Siriwardena, Khaled El Shalakany, Shawn Arnold, Siobhán, Ken Penttinen, Nathan Taylor, William McGraw, Laura Damon, Andrei Krishkevich, Eric Prestemon, Jirat, Brian Thomas Gossett, Ian Dundore, Jason A Saslow, Justin, Jessica Wode, Mark, Caleb Weeks __ Want to find Crash Course elsewhere on the internet? Facebook - http://www.facebook.com/YouTubeCrashCourse Twitter - http://www.twitter.com/TheCrashCourse Tumblr - http://thecrashcourse.tumblr.com Support Crash Course on Patreon: http://patreon.com/crashcourse CC Kids: http://www.youtube.com/crashcoursekids

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Biologie, Chemie: Sekundarstufe II, Hochschule

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Cover: E1 and E2 Reactions: Crash Course Organic Chemistry #22
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Video (13 Minuten)

We’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. Episode Sources: Chemguide.co.uk. Dehydration Of Ethanol To Give Ethene. [online] Available at: https://www.chemguide.co.uk/mechanisms/elim/dhethanol.html [Accessed 21 September 2020] Hornback, J. M. (1998). Organic Chemistry, Brooks. Series Sources: Brown, W. H., Iverson, B. L., Ansyln, E. V., Foote, C., Organic Chemistry; 8th ed.; Cengage Learning, Boston, 2018. Bruice, P. Y., Organic Chemistry, 7th ed.; Pearson Education, Inc., United States, 2014. Clayden, J., Greeves, N., Warren., S., Organic Chemistry, 2nd ed.; Oxford University Press, New York, 2012. Jones Jr., M.; Fleming, S. A., Organic Chemistry, 5th ed.; W. W. Norton & Company, New York, 2014. Klein., D., Organic Chemistry; 1st ed.; John Wiley & Sons, United States, 2012. Louden M., Organic Chemistry; 5th ed.; Roberts and Company Publishers, Colorado, 2009. McMurry, J., Organic Chemistry, 9th ed.; Cengage Learning, Boston, 2016. Smith, J. G., Organic chemistry; 6th ed.; McGraw-Hill Education, New York, 2020. Wade., L. G., Organic Chemistry; 8th ed.; Pearson Education, Inc., United States, 2013. *** Watch our videos and review your learning with the Crash Course App! Download here for Apple Devices: https://apple.co/3d4eyZo Download here for Android Devices: https://bit.ly/2SrDulJ Crash Course is on Patreon! You can support us directly by signing up at http://www.patreon.com/crashcourse Thanks to the following patrons for their generous monthly contributions that help keep Crash Course free for everyone forever: Christine Phelan, Nick, DAVID MORTON HUDSON, Perry Joyce, Scott Harrison, Mark & Susan Billian, Junrong Eric Zhu, Alan Bridgeman, Jennifer Smith, Matt Curls, Tim Kwist, Jonathan Zbikowski, Jennifer Killen, Sarah & Nathan Catchings, Brandon Westmoreland, team dorsey, Trevin Beattie, Eric Koslow, Indika Siriwardena, Khaled El Shalakany, Shawn Arnold, Siobhán, Ken Penttinen, Nathan Taylor, William McGraw, Laura Damon, Andrei Krishkevich, Eric Prestemon, Jirat, Brian Thomas Gossett, Ian Dundore, Jason A Saslow, Justin, Jessica Wode, Mark, Caleb Weeks __ Want to find Crash Course elsewhere on the internet? Facebook - http://www.facebook.com/YouTubeCrashCourse Twitter - http://www.twitter.com/TheCrashCourse Tumblr - http://thecrashcourse.tumblr.com Support Crash Course on Patreon: http://patreon.com/crashcourse CC Kids: http://www.youtube.com/crashcoursekids

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Biologie, Chemie: Sekundarstufe II, Hochschule

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Medien (3)

Cover: Reaktionen - Grundlagen, Ladung, Elektrophile, Nucleophile einfach erklärt - Organische Chemie
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Video

Reaktionen – Grundlagen, Ladung, Elektrophile, Nucleophile einfach erklärt – Organische Chemie. Bei reaktionen betrachtest du die Moleküle, die miteinander reagieren sollen. Liegt ein positiviertes Atom oder eine positive Ladung vor, liegt ein Elektronenmangel vor. Der Mangel kann durch ein Elektronenpaar ausgeglichen werden. Das Paar entspricht entweder einem freien Elektronenpaar oder einem Paar aus einer Mehrfachbindung. Positive Ladung, die durch diesen Schritt entstanden ist, muss ebenfalls wieder ausgeglichen werden. An einem Kohlenstoffatom sind maximal zwei Sauerstoffatome gebunden. Elektrophile sind Teilchen, die einen Elektronenmangel haben. Nucleophile sind Teilchen, die einen Elektronenüberschuss haben. ZUM VIDEO SKELETTSTRUKTUR: http://bit.ly/SkelForm Zur PLAYLIST Organische Chemie: http://bit.ly/OrgaCh ——————————————— ➡ KOSTENLOS ABONNIEREN: http://bit.ly/merkhilfeabo ➡ ALLE KANÄLE: – Nachhilfe & Wissen: https://www.youtube.com/DieMerkhilfe – Wirtschaft: https://www.youtube.com/DieMerkhilfeWirtschaft – Spanisch: https://www.youtube.com/DieMerkhilfeSpanisch ➡ IHR FINDET UNS AUCH HIER! – Instagram: http://www.instagram.com/merkhilfe – Facebook: http://www.facebook.com/merkhilfe – Twitter: http://www.twitter.com/merkhilfe ➡ WAS IST DIE MERKHILFE? Wir sind der Meinung, dass Bildung jedem Menschen kostenlos zur Verfügung stehen soll! Daher findest du auf unseren YouTube-Kanälen moderne Nachhilfe- und Allgemeinwissensvideos für viele Fächer: Biologie, Deutsch, Englisch, Mathe, Geografie, Geschichte, Spanisch, Wirtschaft, Philosophie, Physik, Chemie, Religion, Informatik, Politik, Gesellschaft, Recht und Psychologie. ➡ PRODUKTION DIESES VIDEOS: Script: Sandra Visuelle Konzeption: Henri Ton & Schnitt: Oliver, Henri ➡ COOLE BUCHTIPPS ZUR CHEMIE-PLAYLIST: * Organische Chemie für Dummies: https://amzn.to/2Odtzvj * Anorganische Chemie für Dummies: https://amzn.to/2OWdX4e * Chemie-Abi-Stoff kompakt: https://amzn.to/2OavoJp * Duden Abi-Standardwerk: https://amzn.to/2D6oPWY Alle Zeilen, die mit einem * gekennzeichnet sind, enthalten sog. Affiliate-Links. Sollte ein Kauf zustande kommen, erhalten wir eine kleine Provision von Amazon. Für dich entstehen keine Mehrkosten!

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Chemie: Sekundarstufe I, Sekundarstufe II

Youtube

Cover: MolVis - Molekülvisualisierungen von Reaktionsmechanismen

Interaktives Medium

Reaktionsmechanismen verknüpfen unterschiedliche Stoffklassen miteinander. Die Zusammenhänge werden mit diesem Lerntool deutlich gemacht – und jeder Mechanismus durch dreidimensionale Darstellungen visualisiert.

Interaktives Medium, Unterrichtsbaustein/-reihe, Tool

Chemie: Sekundarstufe II

Cover: Chlorknallgasreaktion - Animation

Interaktives Medium

Bei der Animation von der Chlorknallgasreaktion wird die Zündung eines Chlor-Wasserstoff Gemisches 1:1 mit einem Lichtblitz (Chlorknallgasreaktion) gezeigt. Außerdem kann der Versuch auf der Teilchenebene und aus der energetischen Perspektive betrachte werden. Reaktionsgleichungen der Kettenreaktion werden auch angegeben.

Interaktives Medium, Experiment

Chemie: Sekundarstufe II

Unterrichtsplanung (1)

Cover: MolVis - Molekülvisualisierungen von Reaktionsmechanismen

Interaktives Medium

Reaktionsmechanismen verknüpfen unterschiedliche Stoffklassen miteinander. Die Zusammenhänge werden mit diesem Lerntool deutlich gemacht – und jeder Mechanismus durch dreidimensionale Darstellungen visualisiert.

Interaktives Medium, Unterrichtsbaustein/-reihe, Tool

Chemie: Sekundarstufe II

Praxismaterialien (1)

Cover: Chlorknallgasreaktion - Animation

Interaktives Medium

Bei der Animation von der Chlorknallgasreaktion wird die Zündung eines Chlor-Wasserstoff Gemisches 1:1 mit einem Lichtblitz (Chlorknallgasreaktion) gezeigt. Außerdem kann der Versuch auf der Teilchenebene und aus der energetischen Perspektive betrachte werden. Reaktionsgleichungen der Kettenreaktion werden auch angegeben.

Interaktives Medium, Experiment

Chemie: Sekundarstufe II

Tools (0)

Quellen (0)

Bildungsangebote, Termine, Veranstaltungen (0)

Weitere Inhalte (1)

Cover: Reaktionsmechanismen
hardware

Tool

Veranschaulicht die vielfältigen Reaktionsmechanismen der organischen Chemie

Tool

Chemie: Sekundarstufe I, Sekundarstufe II

Chemie Lernprogramme

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