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\nDiazonium Salts & Nucleophilic Aromatic Substitution: Crash Course Organic Chemistry\n

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\n\nPublisher:\n\nCrash Course\n\n\n
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\nHave you ever wondered where cured meats like salami or pepperoni get their bright red color? Of course its from organic chemistry! A chemical called nitric acid gives them that bright color, while also increasing their shelf. It's also...\nHave you ever wondered where cured meats like salami or pepperoni get their bright red color? Of course its from organic chemistry! A chemical called nitric acid gives them that bright color, while also increasing their shelf. It's also involved in some other interesting reactions. In this episode of Crash Course Organic Chemistry we'll see how nitrous acid reacts with primary amines to form diazonium salts, we'll learn about alkyldiazonium salts and aryldiazonium salts, and see what conditions are necessary for nucleophilic aromatic substitutions.\n
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Resource Details

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Educator Rating
Not yet Rated
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Media Length
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13:38
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Grade
12th - Higher Ed
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Subjects
Science
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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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2022
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Language
English
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Audiences
For Teacher Use
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Fine Print: Educational Use
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Concepts

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john green, education, organic chemistry, nitrogen, electrons
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Additional Tags

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hank green, vlogbrothers, crash course, crashcourse, chemistry, sodium nitrite, nitrous acid, diazonium salt, nitrosyl cation, good leaving, partially positive, groups direct, electron donor, electron withdrawing, leaving group, meta directing, nitrogen gas, nitro group, super stable, aromatic ring, substitution reaction, benzene ring, primary means, group, stable, nucleophilic, primary, nucleophile, learned, means, reaction, mechanism
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Best For: Explaining a topic
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\n\" data-title=\"Get Full Access\" data-container=\"body\" rel=\"popover\" tabindex=\"0\" aria-label=\"Play video: Diazonium Salts & Nucleophilic Aromatic Substitution: Crash Course Organic Chemistry\" href=\"/subscription/new\">\"Diazonium\n\n
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