Talk:Nitrile - Revision history

Wujiayi: /* Synthesis of Benzonitrile from Aniline (Chloe Wu) */ new section

2019-03-10T05:00:41Z

Synthesis of Benzonitrile from Aniline (Chloe Wu): new section

← Older revision		Revision as of 05:00, 10 March 2019
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	[[File:Nitrile_from_Alkene.png\|500px]]		[[File:Nitrile_from_Alkene.png\|500px]]

			== Synthesis of Benzonitrile from Aniline (Chloe Wu) ==

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

2019-02-20T03:08:42Z

Addition of a Nucleophilic Nitrile to an Alkene (Amelia Zoernig): new section

← Older revision		Revision as of 03:08, 20 February 2019
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	[[File:Nitrile_formation_from_halogenalknane_&_CN.png\|1000px]]		[[File:Nitrile_formation_from_halogenalknane_&_CN.png\|1000px]]

			== Addition of a Nucleophilic Nitrile to an Alkene (Amelia Zoernig) ==

			[[File:Nitrile_from_Alkene.png\|500px]]

2019-02-19T22:26:03Z

Synthesis of a nitrile from cyanide and halogenalkane (Tyria Heath): new section

← Older revision		Revision as of 22:26, 19 February 2019
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	In this reaction, benzamine's amine is converted into a diazonium ion after an O=N+ radical adds a nitrogen and removes the hydrogens from the original nitrogen, releasing water in the process and creating a cation. Then, another benzene molecule with an activating, para, ortho directing group such as this methyl group attacks the positively charged diazonium compound and forms a bond with the positive, outermost nitrogen. A proton is lost to reform the conjugation of the attacking benzene ring. This reaction will mainly happen at the para position because of steric hindrance. [[File:Azo_Compound_Formation.png\|800px]]		In this reaction, benzamine's amine is converted into a diazonium ion after an O=N+ radical adds a nitrogen and removes the hydrogens from the original nitrogen, releasing water in the process and creating a cation. Then, another benzene molecule with an activating, para, ortho directing group such as this methyl group attacks the positively charged diazonium compound and forms a bond with the positive, outermost nitrogen. A proton is lost to reform the conjugation of the attacking benzene ring. This reaction will mainly happen at the para position because of steric hindrance. [[File:Azo_Compound_Formation.png\|800px]]

			== Synthesis of a nitrile from cyanide and halogenalkane (Tyria Heath) ==

			[[File:Nitrile_formation_from_halogenalknane_&_CN.png\|1000px]]

2019-02-15T20:16:02Z

Azo Compound Formation Via Aromatic Substitution (Matt Lieberman): new section

← Older revision		Revision as of 20:16, 15 February 2019
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	[[File:Nitrile from Amide .png\|700px]]		[[File:Nitrile from Amide .png\|700px]]

			== Azo Compound Formation Via Aromatic Substitution (Matt Lieberman) ==

			In this reaction, benzamine's amine is converted into a diazonium ion after an O=N+ radical adds a nitrogen and removes the hydrogens from the original nitrogen, releasing water in the process and creating a cation. Then, another benzene molecule with an activating, para, ortho directing group such as this methyl group attacks the positively charged diazonium compound and forms a bond with the positive, outermost nitrogen. A proton is lost to reform the conjugation of the attacking benzene ring. This reaction will mainly happen at the para position because of steric hindrance. [[File:Azo_Compound_Formation.png\|800px]]

2019-01-27T23:30:47Z

Formation of a Nitrile from a Primary Amide Using Thionyl Chloride (Amelia Zoernig): new section

← Older revision		Revision as of 23:30, 27 January 2019
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	[[Main_Page]]		[[Main_Page]]
	__TOC__		__TOC__

			== Formation of a Nitrile from a Primary Amide Using Thionyl Chloride (Amelia Zoernig) ==

			[[File:Nitrile from Amide .png\|700px]]

2019-01-17T19:11:21Z

Cleared out previous entries

← Older revision		Revision as of 19:11, 17 January 2019
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	[[Main_Page]]		[[Main_Page]]
	__TOC__		__TOC__

	~~== 2-phenylacetonitrile ==~~

	~~Christine Solomon~~

	~~[[File:WikiReactionNitrile.png\|1000px]]~~

	~~== 2,2-dimethyl-ethanenitrile (Siyuan Du) ==~~

	~~Dehydration of amide to form nitrile~~

	~~[[File:Nitrile-amide_copy.png\|1100px]]~~

	~~== Letts Nitrile Synthesis (Caleb Lee) ==~~

	~~Synthesis of benzonitrile via Letts Nitrile Synthesis~~

	~~[[File:Letts Nitrile Synthesis.png\|800px]]~~

2018-02-06T04:47:54Z

Letts Nitrile Synthesis (Caleb Lee): new section

← Older revision		Revision as of 04:47, 6 February 2018
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	[[File:Nitrile-amide_copy.png\|1100px]]		[[File:Nitrile-amide_copy.png\|1100px]]

			== Letts Nitrile Synthesis (Caleb Lee) ==

			Synthesis of benzonitrile via Letts Nitrile Synthesis

			[[File:Letts Nitrile Synthesis.png\|800px]]

2018-01-29T02:29:14Z

Dehydration of Amide (Siyuan Du)

← Older revision		Revision as of 02:29, 29 January 2018
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	[[File:WikiReactionNitrile.png\|1000px]]		[[File:WikiReactionNitrile.png\|1000px]]

	== ~~Dehydration of Amide~~ (Siyuan Du) ==		== 2,2-dimethyl-ethanenitrile (Siyuan Du) ==

			Dehydration of amide to form nitrile

	[[File:Nitrile-amide_copy.png\|1100px]]		[[File:Nitrile-amide_copy.png\|1100px]]

2018-01-28T19:01:10Z

Dehydration of Amide (Siyuan Du): new section

← Older revision		Revision as of 19:01, 28 January 2018
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	[[File:WikiReactionNitrile.png\|1000px]]		[[File:WikiReactionNitrile.png\|1000px]]

			== Dehydration of Amide (Siyuan Du) ==

			[[File:Nitrile-amide_copy.png\|1100px]]

2018-01-23T05:14:42Z

2-phenylacetonitrile

← Older revision		Revision as of 05:14, 23 January 2018
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	Christine Solomon		Christine Solomon

	[[File:WikiReactionNitrile.png\|~~1100px~~]]		[[File:WikiReactionNitrile.png\|1000px]]