Consider the mechanism for the reaction of cyclohexene and bromine at -5 °C in CCI,. The bromines in the equation are numbered to differentiate them in the mechanistic steps. 0. Identify the curved arrows needed for the mechanism, then draw the key intermediate and product. Clearly show stereochemistry, by drawing a wedge and dash bond at each chirality center (including hydrogen atoms). Draw one enantiomer for any racemates. +Br,-Br₂ CCI -5°C dibromocyclohexane A. Select the curved arrow(s) needed for step 1. A curved arrow starts from the lone pair of bromine 1 and points to an alkene carbon. Two curved arrows start on bromine 1, each pointing to an alkene carbon. A curved arrow starts from the alkene x bond and points to bromine 1. A curved arrow starts from the Br-Br bond and points to bromine 2. B. Draw 1 organic species and 1 inorganic species formed in step 1. Include charges and non-bonding electrons. Select Draw Rings More // Y C H Br Erase

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Consider the mechanism for the reaction of cyclohexene and bromine at -5 °C in CCI,. The bromines in the equation are
numbered to differentiate them in the mechanistic steps.
0.
Identify the curved arrows needed for the mechanism, then draw the key intermediate and product. Clearly show
stereochemistry, by drawing a wedge and dash bond at each chirality center (including hydrogen atoms). Draw one enantiomer
for any racemates.
CCI
-5°C
+Br,-Br₂ dibromocyclohexane
A. Select the curved arrow(s) needed for step 1.
A curved arrow starts from the lone pair of bromine 1
and points to an alkene carbon.
Two curved arrows start on bromine 1, each pointing to
an alkene carbon.
A curved arrow starts from the alkene x bond and
points to bromine 1.
A curved arrow starts from the Br-Br bond and points
to bromine 2.
B. Draw 1 organic species and 1 inorganic species formed
in step 1. Include charges and non-bonding electrons.
Select
Draw Rings More
/Y
C
H
Br
Erase
Transcribed Image Text:Consider the mechanism for the reaction of cyclohexene and bromine at -5 °C in CCI,. The bromines in the equation are numbered to differentiate them in the mechanistic steps. 0. Identify the curved arrows needed for the mechanism, then draw the key intermediate and product. Clearly show stereochemistry, by drawing a wedge and dash bond at each chirality center (including hydrogen atoms). Draw one enantiomer for any racemates. CCI -5°C +Br,-Br₂ dibromocyclohexane A. Select the curved arrow(s) needed for step 1. A curved arrow starts from the lone pair of bromine 1 and points to an alkene carbon. Two curved arrows start on bromine 1, each pointing to an alkene carbon. A curved arrow starts from the alkene x bond and points to bromine 1. A curved arrow starts from the Br-Br bond and points to bromine 2. B. Draw 1 organic species and 1 inorganic species formed in step 1. Include charges and non-bonding electrons. Select Draw Rings More /Y C H Br Erase
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