English Deutsch Français Italiano Español Português 繁體中文 Bahasa Indonesia Tiếng Việt ภาษาไทย
All categories

Synthesis problem for organic chemistry

to get racemic 2,3-dibromobutane from propyne you have to take propyne through 4 steps. I have figured out that Br2 is one of the steps, but what are the other 3 steps to complete this reaction?

2006-07-27 03:06:58 · 3 answers · asked by wsimms20 1 in Science & Mathematics Chemistry

3 answers

Propyne must first be reacted with sodium to form the alkynide salt. This can then be reacted with methyl iodide to give 2-butyne. The 2-butyne would have to be converted to 2-butene. Reduction with H2 and Pt under pressure would be adequate. The 2-butene could then be reacted with Br2 to give racemic 2,2-dibromobutane. Please note that the above answer of reacting 2-butyne with HBr will give 2,2-dibromobutane not 2,3-dibromobutane.

2006-07-30 11:53:13 · answer #1 · answered by Richard 7 · 0 0

Meso-2 3-dibromobutane

2016-11-09 19:43:23 · answer #2 · answered by Anonymous · 0 0

1st step

CH3Br, NaH or LiNH2 to make 2-Butyne

Now treat with HBr

2006-07-27 03:11:57 · answer #3 · answered by ag_iitkgp 7 · 0 0

fedest.com, questions and answers