organic chemistry Elimination reaction with 1,2dibromo4
1 Bromo 1 Methylcyclohexane. The first set of conditions favors the e2 process, because sodium ethoxide is a strong base.two elimination products are. Web view the full answer transcribed image text:
organic chemistry Elimination reaction with 1,2dibromo4
The alkyl bromide is tertiary. Thus, dehydrohalogenation of this compound gives only one alkene. Web view the full answer transcribed image text: Predict the products of this reaction,. One ether and two alkenes. The first set of conditions favors the e2 process, because sodium ethoxide is a strong base.two elimination products are.
The alkyl bromide is tertiary. Predict the products of this reaction,. Web view the full answer transcribed image text: The alkyl bromide is tertiary. The first set of conditions favors the e2 process, because sodium ethoxide is a strong base.two elimination products are. Thus, dehydrohalogenation of this compound gives only one alkene. One ether and two alkenes.
