Talk:Alkyl Halide: Difference between revisions
Jump to navigation
Jump to search
→Synthesis of bromopropane from propanol (Reese Zhu): new section |
|||
| Line 1: | Line 1: | ||
[[Main_Page]] | [[Main_Page]] | ||
__TOC__ | __TOC__ | ||
== 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. [[File:Alkyl_Halide.png]] | |||
== Synthesis of bromopropane from propanol (Reese Zhu) == | == 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. [[File:Alkyl_Halide.png]] | The hydroxyl group attacks the proton on HBr and leaves as water, followed by bromide ion attacking the carbo cation. [[File:Alkyl_Halide.png]] | ||
Revision as of 06:41, 28 January 2019
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 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.