consider the reaction of 1-methltcyclopentane with water and
Cl2 to answer questions a-e.
A.) this reaction is an example of ________ (electrophilic
substitution, electrophilic addition, elimination, carbocation
rearrangement, nucleophilic addition)
B.) it occurs with ________ stereoselectivity
(Anti, syn, no)
C.) the observed stereoselectivity can be explained on the
basis of formation of ______ during the course of this
reaction
(Planar carbocation intermediate, oxonium ion intermediate,
4-membered cyclic transition state, bridged chloronium ion
intermediate)
D.) the electrophile in the first step (formation of the first
intermediate) is ________.
E.) provide the names or structures of the two nucleophiles in
this reaction.