per The following alkene is treated with one equivalent of N-Bromosuccinimide in dichloromethane in the presence of light to give Draw a line-angle formula for each product formed. You do not have to consider stereochemistry. Draw organic products only. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. •Separate multiple products using the + sign from the drop-down menu. ChemDoodle 成文的 00- Air

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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apter 8
The following alkene is treated with one equivalent of N-Bromosuccinimide in dichloromethane in the presence of light to give bromination product(s).
Draw a line-angle formula for each product formed.
You do not have to consider stereochemistry.
• Draw organic products only.
•
Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
• Separate multiple products using the + sign from the drop-down menu.
98
ChemDoodle
4
00- AIF
Transcribed Image Text:apter 8 The following alkene is treated with one equivalent of N-Bromosuccinimide in dichloromethane in the presence of light to give bromination product(s). Draw a line-angle formula for each product formed. You do not have to consider stereochemistry. • Draw organic products only. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple products using the + sign from the drop-down menu. 98 ChemDoodle 4 00- AIF
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