New bonds are formed at both the carbon atoms of the alkene double bond and at Br. The bridged bromonium ions are not the only species formed in this step.

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Chapter1: Chemical Foundations
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Consider the reaction of 1-methylcyclohexene with Br2 in CH3OH.

Draw a curved arrow mechanism for Step 1 of this reaction, showing the formation of the intermediate(s), including stereochemistry. Show all intermediate structures for this step.

1. Draw the curved arrow mechanism for step 1 in this reaction.

2. Draw the structure(s) of the intermediate(s) formed in step 1 of this reaction.

New bonds are formed at both the carbon atoms of the alkene double bond and at Br.
x
O
The bridged
bromonium ions
are not the only
species formed in
this step.
Transcribed Image Text:New bonds are formed at both the carbon atoms of the alkene double bond and at Br. x O The bridged bromonium ions are not the only species formed in this step.
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