Organic Chemistry Wiki Spring 2019 - User contributions [en]

Talk:Ether

2019-05-09T01:33:53Z

Heathtyr: /* Synthesis of Benzyl Phenyl Ether */

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== Diethyl Ether (Matt Lieberman) ==

Ethanol reacts with phosphorus tribromide to create ethyl bromide. Ethyl bromide can then react with more ethanol to create diethyl ether. Byproducts of the reaction are water and an increase of the acidity of the solution. [[File:Production of Ether.png|900px]]

== Williamson Ether Synthesis (Alyssa Radakovich) ==

A reaction of a methoxy group with butyl bromide forms methoxy butane.
[[File:Wiki_Reaction_Collection1.png|1000px]]

== Mitsunobu Reaction - Steven Sharpe ==

Triphenylphosphine and DEAD react with the OH on the alcohol. The ETOH substitutes for the new compound, forming the ether.
[[File:WIKI Reaction 1 - Mitsunobu.png|800px]]

== 2-(2-formylphenoxy)acetic acid (Abena Afari). ==

A reaction of 2-hydroxybenzaldehyde with 2-chloroacetic acid and sodium hydroxide in the presence of heat to form 2-(2-formylphenoxy)acetic acid. [[File:Ether_Synthesis_AA.png|500px]]

[[File:Synthesis_of_anisole.png]]

== Synthesis of Anisole (Tyria Heath) ==

[[File:Synthesis_of_anisole.png|1100px]]

== Ether Synthesis - Erica Satchell ==

[[File:Wiki_assgn_3.png|600ppx]]

== Pyridine: ether formation (Reese Zhu)==

[[File:Pyridine_(ether_formation).png|1000px]]

== Synthesis of Benzyl Phenyl Ether (Tyria Heath) ==

[[File:Preparation-of-benzyl-phenyl-ether.png|1000px]]

Talk:Ether

2019-05-09T01:33:35Z

Heathtyr: /* Synthesis of Benzyl Phenyl Ether */ new section

[[Main_Page]]
__TOC__

== Diethyl Ether (Matt Lieberman) ==

Ethanol reacts with phosphorus tribromide to create ethyl bromide. Ethyl bromide can then react with more ethanol to create diethyl ether. Byproducts of the reaction are water and an increase of the acidity of the solution. [[File:Production of Ether.png|900px]]

== Williamson Ether Synthesis (Alyssa Radakovich) ==

A reaction of a methoxy group with butyl bromide forms methoxy butane.
[[File:Wiki_Reaction_Collection1.png|1000px]]

== Mitsunobu Reaction - Steven Sharpe ==

Triphenylphosphine and DEAD react with the OH on the alcohol. The ETOH substitutes for the new compound, forming the ether.
[[File:WIKI Reaction 1 - Mitsunobu.png|800px]]

== 2-(2-formylphenoxy)acetic acid (Abena Afari). ==

A reaction of 2-hydroxybenzaldehyde with 2-chloroacetic acid and sodium hydroxide in the presence of heat to form 2-(2-formylphenoxy)acetic acid. [[File:Ether_Synthesis_AA.png|500px]]

[[File:Synthesis_of_anisole.png]]

== Synthesis of Anisole (Tyria Heath) ==

[[File:Synthesis_of_anisole.png|1100px]]

== Ether Synthesis - Erica Satchell ==

[[File:Wiki_assgn_3.png|600ppx]]

== Pyridine: ether formation (Reese Zhu)==

[[File:Pyridine_(ether_formation).png|1000px]]

== Synthesis of Benzyl Phenyl Ether ==

[[File:Preparation-of-benzyl-phenyl-ether.png|1000px]]

File:Preparation-of-benzyl-phenyl-ether.png

2019-05-09T01:32:40Z

Heathtyr:

Talk:Ether

2019-03-11T02:51:58Z

Heathtyr: /* Synthesis of Anisole (Tyria Heath) */ new section

Talk:Ether

2019-03-11T02:49:12Z

Heathtyr: /* Synthesis of Anisole (Tyria Heath) */

Talk:Ether

2019-03-11T02:48:30Z

Heathtyr: /* Synthesis of Anisole (Tyria Heath) */ new section

[[Main_Page]]
__TOC__

== Diethyl Ether (Matt Lieberman) ==

Ethanol reacts with phosphorus tribromide to create ethyl bromide. Ethyl bromide can then react with more ethanol to create diethyl ether. Byproducts of the reaction are water and an increase of the acidity of the solution. [[File:Production of Ether.png|900px]]

== Williamson Ether Synthesis (Alyssa Radakovich) ==

A reaction of a methoxy group with butyl bromide forms methoxy butane.
[[File:Wiki_Reaction_Collection1.png|1000px]]

== Mitsunobu Reaction - Steven Sharpe ==

Triphenylphosphine and DEAD react with the OH on the alcohol. The ETOH substitutes for the new compound, forming the ether.
[[File:WIKI Reaction 1 - Mitsunobu.png|800px]]

== 2-(2-formylphenoxy)acetic acid (Abena Afari). ==

A reaction of 2-hydroxybenzaldehyde with 2-chloroacetic acid and sodium hydroxide in the presence of heat to form 2-(2-formylphenoxy)acetic acid. [[File:Ether_Synthesis_AA.png|500px]]

== Synthesis of Anisole (Tyria Heath) ==

[[File:Synthesis_of_anisole.png}|1000px]]

File:Synthesis of anisole.png

2019-03-11T02:46:27Z

Heathtyr:

Talk:Nitrile

2019-02-19T22:26:03Z

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

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

[[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]]

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

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

File:Nitrile formation from halogenalknane & CN.png

2019-02-19T22:23:51Z

Heathtyr:

File:Addition of grignards to aldehydes.png

2019-02-11T03:28:21Z

Heathtyr:

Talk:Alcohol

2019-02-11T03:24:23Z

Heathtyr: /* addition of Grignards to Aldehydes (Tyria Heath) */ new section

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== SN2 Epoxide Opening with Grignard Reagent - Anne Steensma ==

[[File:Sn2 epoxide to alcohol.png|800px]]

== ethanal to 1-phenyl ethan-1-ol George Kaslow ==

[[File:Untitled_Document-1.png]]

== Primary Alcohol to Carboxylic Acid - Emily Mamrak ==

[[File:Primary-alcohol-to-carboxylic-acid.png]]

== Dihydroxylation of alkene - Klarie Li ==

[[File:Dihydroxylation.png|600px]]

== addition of Grignards to Aldehydes (Tyria Heath) ==

[[File:Addition_of_grignards_to_aldehydes.png|1000px]]

Talk:Aldehyde

2019-01-27T05:25:24Z

Heathtyr: /* addition of Grignards to Aldehydes (Tyria Heath) */ new section

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== Propanal (Nora Liu) ==

A reaction of 1-bromopropane with NaOH and then PCC to form propanal[[File:Propanal (Nora Liu).png|880px]]

== Benzaldehyde (Kyle Dixon-Anderson) ==

The reductive amination of Benzaldehyde with Sodium cyanoborohydride and Aniline into Phenylmethanamine

[[File:Reductive Amination of Benzaldehyde.png]]

== addition of Grignards to Aldehydes (Tyria Heath) ==

[[File:Addition_of_grignards_to_aldehydes_(Tyria_Heath).png|1000px]]

File:Addition of grignards to aldehydes (Tyria Heath).png

2019-01-27T05:23:43Z

Heathtyr: Heathtyr uploaded a new version of File:Addition of grignards to aldehydes (Tyria Heath).png

File:Addition of grignards to aldehydes (Tyria Heath).png

2019-01-27T05:16:55Z

Heathtyr: