Talk:Alkyl Halide: Difference between revisions

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== Sn1 reaction for alkyl bromide formation ==
[[Main_Page]]
__TOC__


[[File:Alkylhaliderxn.png|1100px]]
== Synthesis of bromopropane from propanol (Reese Zhu) ==


== Finkelstein Reaction (SN2): Bromoethane to Iodoethane ==
The hydroxyl group attacks the proton on HBr and leaves as water, followed by bromide ion attacking the carbo cation. [[File:Alkyl_Halide.png]]


[[File:CHM-WIKI2.PNG|1100px]]
== Synthesis of chlorobutane from butanol (Derrick Okine) ==


== Alkyl halide formation from alkene ==
The hydroxyl group attacks the proton on HCl and leaves as water, followed by chloride ion attacking the carbo cation. [[File:1.png]]


[[File:JD Chem Wiki.png|1100px]]
== Alkyl Halide Formation ==


== SN2 substitution of alcohol to form ethyl chloride (Alkyl Halide) ==
In this procedure, convert carboxylic acid to acyl chloride with SOCl2. Then reduce the carbonyl carbon so as to remove the carbonyl from the compound with a combination of Sn and HCl.
[[File:Alkyl Halide Formation.png|850px]]


[[File:Assignment.jpeg]]
== Synthesis of Bromobenzene from Aniline (Nichole Hannan) ==


== Fredyl-Crafts Acylation of benzene with chloroethane ==
Two step synthesis of Bromobenzene from Aniline using sodium nitrate and CuBr.
[[File:Bromobenzene_synthesis.png|800px]]


[[File:fredyl-crafts acylation.jpg]]
== radical reaction (Nora Liu)  ==


== Eletrophillic Aromatic Substitution of a Bromine ==
[[File: Radical_reaction_(Nora_Liu).png|600px]]
 
[[File:brominesu.jpg]]
 
== Alkyl halide Bromine ==
 
[[File:Alkyl_halide_Bromine.png|1100px]]
 
== Anti-Markovnikov Bromine Addition to Cyclohexene ==
 
[[File:HBR.jpeg]]
 
== Radical Reduction of Alkene with Benzoyl peroxide and Hydrogen bromide ==
 
[[File:Radical_Reduction_of_Alkene_with_Benzoyl_peroxide.png]]
 
== Radical addition of chlorine to ethane  ==
 
[[File:wiki3chem.jpg]]
 
== Allylic Bromination ==
 
[[File:Allylic_Bromination.png]]
 
== Chloromethylation of heterocycle (indole) ==
 
[[File:chloromethylation.jpg]]

Latest revision as of 21:08, 10 March 2019

Main_Page

Synthesis of bromopropane from propanol (Reese Zhu)

The hydroxyl group attacks the proton on HBr and leaves as water, followed by bromide ion attacking the carbo cation.

Synthesis of chlorobutane from butanol (Derrick Okine)

The hydroxyl group attacks the proton on HCl and leaves as water, followed by chloride ion attacking the carbo cation.

Alkyl Halide Formation

In this procedure, convert carboxylic acid to acyl chloride with SOCl2. Then reduce the carbonyl carbon so as to remove the carbonyl from the compound with a combination of Sn and HCl.

Synthesis of Bromobenzene from Aniline (Nichole Hannan)

Two step synthesis of Bromobenzene from Aniline using sodium nitrate and CuBr.

radical reaction (Nora Liu)

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