Talk:Nitro compound - Revision history

Clarkeka19: /* Nitration of Furan (Kaia Clarke) */

2019-05-11T21:03:01Z

Nitration of Furan (Kaia Clarke)

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	== Nitration of Furan (Kaia Clarke) ==		== Nitration of Furan (Kaia Clarke) ==

	[[File:~~Nitration of Furan~~]]		[[File:Screen Shot 2019-05-11 at 3.58.44 PM.png]]

2019-05-11T21:01:58Z

Nitration of Furan (Kaia Clarke): new section

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	[[File:Nitro_Compound_Synthesis.png\|400px]]		[[File:Nitro_Compound_Synthesis.png\|400px]]

			== Nitration of Furan (Kaia Clarke) ==

			[[File:Nitration of Furan]]

2019-05-10T00:34:36Z

Nitro Compound Synthesis - Klarie Li: new section

← Older revision		Revision as of 00:34, 10 May 2019
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	The sulfuric acid protonates the hydroxyl group on the nitric acid, which leaves as water. The remaining molecule is an unstable positively charged nitrogen double-bonded to two oxygens. One of the carbon atoms in the benzene ring attacks this compound at the nitrogen, giving both oxygens partial-negative charges and making the overall charge of the nitro group more stable. However, this leaves a positive charge in the pi system of the benzene ring which is compensated for by loss of a proton at the ipso carbon. [[File:Nitro Compound Formation.png\|800px]]		The sulfuric acid protonates the hydroxyl group on the nitric acid, which leaves as water. The remaining molecule is an unstable positively charged nitrogen double-bonded to two oxygens. One of the carbon atoms in the benzene ring attacks this compound at the nitrogen, giving both oxygens partial-negative charges and making the overall charge of the nitro group more stable. However, this leaves a positive charge in the pi system of the benzene ring which is compensated for by loss of a proton at the ipso carbon. [[File:Nitro Compound Formation.png\|800px]]

			== Nitro Compound Synthesis - Klarie Li ==

			[[File:Nitro_Compound_Synthesis.png\|400px]]

2019-02-11T03:56:14Z

NItro Compound Formation (Matt Lieberman): new section

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	[[Main_Page]]		[[Main_Page]]
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			== NItro Compound Formation (Matt Lieberman) ==

			The sulfuric acid protonates the hydroxyl group on the nitric acid, which leaves as water. The remaining molecule is an unstable positively charged nitrogen double-bonded to two oxygens. One of the carbon atoms in the benzene ring attacks this compound at the nitrogen, giving both oxygens partial-negative charges and making the overall charge of the nitro group more stable. However, this leaves a positive charge in the pi system of the benzene ring which is compensated for by loss of a proton at the ipso carbon. [[File:Nitro Compound Formation.png\|800px]]

2019-01-17T19:12:08Z

Cleared out previous entries

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	~~== Nitration of Benzene through aromatic substitution. Jacob Byerly-Duke ==~~

	~~[[File:Byerlydu_benzene_nitration.png\|700px]]~~

	~~== Nitration of Furan (Madison Wardlaw) ==~~

	~~[[File:Wiki_assignment_3.png\|850px]]~~
	~~Nitration of furan through electrophilic substitution mechanism and acid catalyst~~

	~~== Quinoline Reaction (Grace Park) ==~~

	~~[[File:Untitled.png]]~~

2018-05-11T13:54:19Z

Quinoline Reaction (Grace Park): new section

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	[[File:Wiki_assignment_3.png\|850px]]		[[File:Wiki_assignment_3.png\|850px]]
	Nitration of furan through electrophilic substitution mechanism and acid catalyst		Nitration of furan through electrophilic substitution mechanism and acid catalyst

			== Quinoline Reaction (Grace Park) ==

			[[File:Untitled.png]]

2018-05-08T01:47:38Z

Nitration of Furan (Madison Wardlaw): new section

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	[[File:Byerlydu_benzene_nitration.png\|700px]]		[[File:Byerlydu_benzene_nitration.png\|700px]]

			== Nitration of Furan (Madison Wardlaw) ==

			[[File:Wiki_assignment_3.png\|850px]]
			Nitration of furan through electrophilic substitution mechanism and acid catalyst

2018-02-02T16:36:11Z

Nitration of Benzene through aromatic substitution. Jacob Byerly-Duke: new section

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	[[Main_Page]]		[[Main_Page]]
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			== Nitration of Benzene through aromatic substitution. Jacob Byerly-Duke ==

			[[File:Byerlydu_benzene_nitration.png\|700px]]

2018-01-19T18:31:50Z

Cleared page for spring semester use

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	~~== Nitrobenzene (Lila Cardozo) ==~~
	~~A reaction of benzene with nitric acid to form nitrobenzene.~~
	~~[[File:Wiki1 nitro.png\|1100px]]~~

	~~== By treating tertiary amines with alkaline KMnO4 this gives tertiary nitro compounds. Only with tertiary amines. Alfredo Villalobos-Perez ==~~

	~~[[File:Formation of Nitromethane.png\|1100px]]~~

	~~== Reduction of Nitrobenzene by HCl, Sn Brian Sands ==~~

	~~[[File:Nitrobenzene-reduction.png]][http://organicchem.sites.grinnell.edu/wiki/spring19/images/9/98/Nitrobenzene-reduction.png]~~

	~~== Nitration of Pyrrole: Sophie Banegas ==~~

	~~[[File:Nitration of Pyrrole.png]]~~

	~~== Nitration of Indole - Emma Olson ==~~

	~~[[File:Indole_Nitration.jpg\|900px]]~~

2017-05-12T02:09:01Z

Nitration of Indole - Emma Olson

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	== Nitration of Indole - Emma Olson ==		== Nitration of Indole - Emma Olson ==

	[[File:Indole_Nitration.jpg\|~~1100px~~]]		[[File:Indole_Nitration.jpg\|900px]]