CH
21
Test
Bank
E.
III
>
I
>
II
>
IV
(most
acidic
H
=
closest
to
carbonyl/EN
groups
bUT
NOT
ESTER!)
D.
IV
E.
both
B
and
C
26.
Provide
both
resonance
structures
of
the
enolate
formed
when
the
following
ketone
is
treated
with
a
base.
A.
I
E.
none
of
these CH
21
Test
Bank
C.
III
1.
PCC/CH2Cl2
2.
H3O+/Br2
3.
NaOCH2CH3
1.
PCC/CH2Cl2
2.
H3O+/Br2
3.
NaCN
A.
I CH
21
Test
Bank
36.
Predict
the
major
product
for
the
following
reaction
and
provide
a
curved
arrow
mechanism
for
the
formation
of
the
product.
B.
II
E.
none
of
these
C.
III
1.
H3O+/heat
2.
Br2/PBr3
3.
H2O
E.
V
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