Talk:Amine: Difference between revisions

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[[Main_Page]]
== N-ethylcyclohexanimine (Maverick Zhang) ==
__TOC__


== Reduction reaction with lithium aluminium hydride gives a phenylmethanamine from a benzonitrile (Rong Guo)==
[[File:Untitled_Document-1.png|1100px]]


[[File:Untitled.png|900px]]
Cyclohexanone reacts with ethanamine in acidic condition to form N-ethylcyclohexanimine.


== Synthesis of Second-Degree Amine from Aldehyde - Emma Olson ==
== N-methyl-1-phenylmethanamine (Michael Hewitt) ==


[[File:2Amine_Synthesis.png|800px]]
[[File:Screen_Shot_2018-02-04_at_7.43.06_PM.png]]


== Brian Sands Week 1 Submission: Simple Amine reacts with Grignard Reagent ==
== Enamine formation (Edward Lopatto) ==


[http://organicchem.sites.grinnell.edu/s18/wiki/images/9/9e/Screenshot_%2833%29.png]
Reaction of a second-degree amine with a ketone to form an enamine.
[[File:Enamine_formation.png|800px]]


== Formation of aniline with nitrobenzene and tetrahydrothiophene 1,1-dioxide :Jason Jennings  ==
== Butanamine (Matthew Palmeri) ==


[[File:Amine.png]]
[[File:Butanamine_Wiki_entry_2.png|1000px]]


== Reduction with an amide (Hannah Hong) ==
== Formation of Amine from Nitro group (Kelsey Zhang) ==


[[File:Wiki_3.png|1100px]]
[[File: Reduction_of_amide.png|1100px]]
The formation of Amine from Nitro group with Tin in acidic condition
 
==2-aminobutanal (Mikayla Kricfalusi)==
 
[[File:2-aminobutanal (Mikayla Kricfalusi).png|1000px]]
 
== Second synthesis of 2-aminobutanal (Mikayla Kricfalusi)==
 
[[File:Amino_acid_again.png|1000px]]
 
== Strecker Synthesis (Matthew Record) ==
 
[[File:Strecker_Synthesis.png|1100px]]
 
== Aniline synthesis from chlorobenzene (Jacob Morsch) ==
 
[[File:Aniline_Synthesis.png|800px]]
 
== Imine Reduction (Gabi Gryc) ==
 
[[File:Imine reduction.png|1000px]]
 
== Gabriel Synthesis (Caleb Lee) ==
 
[[File:GabrielSynthesis.png|1000px]]

Latest revision as of 19:22, 14 May 2018

N-ethylcyclohexanimine (Maverick Zhang)

Cyclohexanone reacts with ethanamine in acidic condition to form N-ethylcyclohexanimine.

N-methyl-1-phenylmethanamine (Michael Hewitt)

Enamine formation (Edward Lopatto)

Reaction of a second-degree amine with a ketone to form an enamine.

Butanamine (Matthew Palmeri)

Formation of Amine from Nitro group (Kelsey Zhang)

The formation of Amine from Nitro group with Tin in acidic condition

2-aminobutanal (Mikayla Kricfalusi)

Second synthesis of 2-aminobutanal (Mikayla Kricfalusi)

Strecker Synthesis (Matthew Record)

Aniline synthesis from chlorobenzene (Jacob Morsch)

Imine Reduction (Gabi Gryc)

Gabriel Synthesis (Caleb Lee)

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