In the double elimination reaction involving the synthesis of diphenylacetylene from meso 1,2-dibromo-1,2-diphenylethane shown, which of the two steps is rate determining and why?

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter13: Substitution
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In the double elimination reaction involving the synthesis of diphenylacetylene from meso 1,2-dibromo-1,2-diphenylethane shown, which of the two steps is rate determining and why? 

 

 

H
Ph,
Br
H
Br
Ph
но
OH
\'Ph
"Br
Ph
Br
Br
Ph
Ph
Figure 2. Mechanism for Dehydrobromination of Stilbene Dibromide
Bry
КОн
-CEC-
Ph
Ph
Но
Он
Figure 3. Mechanism for Dehydrobromination of (E)-1-Bromo-1,2-diphenylethylene
I'"
II
I
Transcribed Image Text:H Ph, Br H Br Ph но OH \'Ph "Br Ph Br Br Ph Ph Figure 2. Mechanism for Dehydrobromination of Stilbene Dibromide Bry КОн -CEC- Ph Ph Но Он Figure 3. Mechanism for Dehydrobromination of (E)-1-Bromo-1,2-diphenylethylene I'" II I
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