Identify the major organic product generated from the reaction shown. D 1 + enantiomer CH3 none of these CH3 D || D + enantiomer D₂ Pd ? CH3 H D + enantiomer IM D CH3 What is wrong with the following mechanism? H₂O Br Br The arrow indicating the formation of the C-Br bond (nucleophilic attack) should start at the bromide anion. An arrow is also needed to indicate the loss of the leaving group. None of these The arrow should be removing a proton from the H2O group. There is no leaving group, so there should be no arrows.

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Identify the major organic product generated from the reaction shown.
D
1
+ enantiomer
CH3
none of these
CH3
D
||
D
+ enantiomer
D₂
Pd
?
CH3
H
D
+ enantiomer
IM
D
CH3
Transcribed Image Text:Identify the major organic product generated from the reaction shown. D 1 + enantiomer CH3 none of these CH3 D || D + enantiomer D₂ Pd ? CH3 H D + enantiomer IM D CH3
What is wrong with the following mechanism?
H₂O
Br
Br
The arrow indicating the formation of the C-Br bond (nucleophilic attack) should
start at the bromide anion.
An arrow is also needed to indicate the loss of the leaving group.
None of these
The arrow should be removing a proton from the H2O group.
There is no leaving group, so there should be no arrows.
Transcribed Image Text:What is wrong with the following mechanism? H₂O Br Br The arrow indicating the formation of the C-Br bond (nucleophilic attack) should start at the bromide anion. An arrow is also needed to indicate the loss of the leaving group. None of these The arrow should be removing a proton from the H2O group. There is no leaving group, so there should be no arrows.
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