|
|
| Line 1: |
Line 1: |
| == N-ethylcyclohexanimine (Maverick Zhang) ==
| | [[Main_Page]] |
| | | __TOC__ |
| [[File:Untitled_Document-1.png|1100px]]
| |
| | |
| Cyclohexanone reacts with ethanamine in acidic condition to form N-ethylcyclohexanimine.
| |
| | |
| == N-methyl-1-phenylmethanamine (Michael Hewitt) ==
| |
| | |
| [[File:Screen_Shot_2018-02-04_at_7.43.06_PM.png]] | |
| | |
| == Enamine formation (Edward Lopatto) ==
| |
| | |
| Reaction of a second-degree amine with a ketone to form an enamine.
| |
| [[File:Enamine_formation.png|800px]]
| |
| | |
| == Butanamine (Matthew Palmeri) ==
| |
| | |
| [[File:Butanamine_Wiki_entry_2.png|1000px]]
| |
| | |
| == Formation of Amine from Nitro group (Kelsey Zhang) ==
| |
| | |
| [[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]]
| |