exam 3 reviews

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1

O

NaBH

4

1)

OH

OH

OH

H

H

+

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2

O

O

LiAlH

4

OH

2)

O

PhMgBr

HO

3)

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3

O

Tollens reagent

No reaction

Ag

2

O and NH

4

OH are the Tollens

reagent

4)

O

Na

HO

5)

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4

6) Draw sodium acetate.

O

O

Na

7) Draw cycloheptanecarboxylic
acid.

O

OH

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5

8) Draw 4-hexenal.

O

O

9) Draw 2,4-
pentanedione.

O

O

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6

10) Draw benzene-1,3-
dicarboxaldehyde.

O

O

11) Draw the product(after workup) of 3-methyl-2-
cyclohexenone with methyl Grignard.

O

MgBr

HO

HO

HO

+

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7

12) Draw the product(after workup) of
3-methyl-2-cyclohexenone with H

2

./Pd-

C.

O

H

2

/Pd-C

O

O

O

+

H

H

13) Draw the keto tautomer of this
enol.

OH

OH

H

OH

H

O

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8

14) Pentane-2,4-dione exists as a tautomeric mixture
of 8% keto and 92% enol. Draw the enol form.

O

O

O

O

O

O

OH

O

HO

O

+

The Z isomer is preferred due
to the stabilization provided
by hydrogen bonding.

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9

15)

O

OH

LiAlH

4

OH

O

Cl

excess PhMgBr

dilute acid

16)

HO

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10

17
)

O

OCH

2

CH

3

LiAlH

4

OH

18)

O

O

excess PhMgBr

HO

OH

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11

O

O

O

O

O

O

H

2

O

HO

OH

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12

19)

H

3

CH

2

CO

O

OCH

2

CH

3

excess PhMgBr

HO

H

3

CH

2

CO

O

OCH

2

CH

3

Ph

H

3

CH

2

CO

O

OCH

2

CH

3

Ph

H

3

CH

2

CO

O

Ph

Ph

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13

H

3

CH

2

CO

O

Ph

Ph

Ph

O

Ph

Ph

Ph

O

Ph

Ph

H

2

O

Ph

OH

Ph

Ph

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14

20)

OH

Na

2

Cr

2

O

7

H

2

SO

4

OH

O

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15

19..29a) Draw 3,3’-dimethylpentanoic
acid.

e) Draw m-hydroxybenzoic acid

O

OH

HO

O

OH

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16

19.32
a)

OH

CrO

3

H

2

SO

4

, H

2

O

OH

O

b)

KMnO

4

O

HO

O

OH

c)

O

3

H

2

O

OH

O

+

O

C

O

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17

d)

R

H

2

C

OH

Na

2

Cr

2

O

7

H

2

SO

4

, H

2

O

R

C

OH

O

BH

3

H

2

O

2

, -OH

19.33a)

OH

CrO

3

H

2

SO

4

, H

2

O

OH

O

b)

NaNH

2

CH

3

I

NaNH

2

CH

3

CH

2

I

H

3

CH

2

C

CH

3

O

3

H

2

O

O

OH

O

OH

+

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18

c)

(CH

3

)

2

CHCl

AlCl

3

KMnO

4

O

OH

.

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19

19.37) In each group choose which compound is
most acidic. Also choose which has the strongest
conjugate base.

a)

O

OH

O

OH

O

OH

Br

Cl

Most acidic

Strongest
conjugate
base

b
)

OH

O

2

N

OH

Cl

OH

Most acidic

Strongest
conjugate
base

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20

O

H

2

/Pd-C

NaBH

4

MeOH

LiAlH

4

H

2

O

20.3
7)

OH

PCC

OH

O

No
reaction

Na

2

Cr

2

O

7

H

2

SO

4

, H

2

O

Ag

2

O

NH

4

OH

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21

O

CH

3

MgBr

H

2

O

CH

3

Li

H

2

O

(CH

3

)

2

CuLi

H

2

O

CNa

H

2

O

CLi

H

2

O

TBDMSCl

imidazole

OH

No reaction

OH

OTBDMS

O

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22

20.38)

H

2

/Pd-C

NaBH

4

MeOH

LiAlH

4

H

2

O

O

OH

PCC

Na

2

Cr

2

O

7

H

2

SO

4

, H

2

O

Ag

2

O

NH

4

OH

No reaction

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23

CH

3

MgBr

H

2

O

CH

3

Li

H

2

O

O

OH

CNa

H

2

O

CNa

H

2

O

HO

TBDMSCl

imidazole

No reaction

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24

20.40)

MgBr H

3

CH

2

C

OH

CO

2

H

3

O

+

O

+

H

3

CH

2

C

O

OH

O

OH

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25

20.41)

O

Cl

R

2

CuLi

R

2

CuLi

O

OEt

R

2

CuLi

O

R

2

CuLi

O

O

R

No reaction

O

R

OH

R

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26

20.4
7)

NaBH

4

MeOH

LiAlH

4

H

2

O

LiAlH

4

H

2

O

O

O

OCH

3

OH

O

OCH

3

OH

OH

(H

3

C)

2

N

OH

(H

3

C)

2

N

O

O

OH

Cl

O

O

OH

LiAlH

(OC(CH

3

)

3

)

3

H

2

O

HO

O

OH

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27

21.46)

O

NaCN

HCl

Ph

3

P

CHCH

3

(H

3

C)

2

HC

NH

2

H

3

O

+

OH

CN

NCH(CH

3

)

2

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28

O

CH

2

CH

3

H

N

H

3

O

+

H

3

CH

2

C

excess EtOH

TsOH

HO

OH

TsOH

N(CH

2

CH

3

)

2

OCH

2

CH

3

OCH

2

CH

3

O

O

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29

21.54)

Br

2

FeBr

3

Br

CH

3

COCl

AlCl

3

Br

O

HO

OH

TsOH

Br

O

O

Mg

MgBr

O

O

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30

MgBr

O

O

O

H

2

O

O

O

OH

PCC

O

O

O

H

2

O

H

3

O

+

O

O

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31

NH

O

H

2

O

HCl, heat

1)

NH

2

O

OH

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32

NH

O

H

Cl

NH

OH

H

2

O

NH

HO

H

O

H

Cl

NH

HO

OH

H

Cl

NH

2

HO

OH

NH

2

HO

OH

Cl

NH

2

O

OH

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33

2)

O

O

O

H

2

O

O

HO

O

OH

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34

3)

O

O

O

excess CH

3

OH

HCl

O

O

O

O

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35

4)

CN

aq. H

2

O

20 C

O

H

2

N

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36

5)

NH

2

O

OCH

2

CH

3

H

N

O

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37

O

O

excess H

2

O

HCl

6)

O

HO

OH

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38

7
)

O

O

O

excess NH

3

O

NH

2

O

OH

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39

8)

O

Cl

CH

3

CH

2

OH

O

O

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40

9)

OH

O

O

O

O

O

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41

10
)

NH

2

O

O

O

O

N

H

O

OH

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42

11)

O

OCH

3

CH

3

NH

2

O

NHCH

3

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43

12
)

O

OH

O

OCH

2

CH

2

CH

3

O

OH

O

Cl

SOCl

2

O

Cl

O

OCH

2

CH

2

CH

3

CH

3

CH

2

CH

2

OH

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44

13
)

O

NH

2

O

Cl

O

NH

2

O

OH

H

2

O

H

+

, heat

O

OH

O

Cl

SOCl

2

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45

14)

OH

O

OH

OH

Cl

SOCl

2

Cl

NaCN

N

N

H

2

O

H

+

, heat

O

OH

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46

15)

O

N

H

O

OH

KMnO

4

heat

O

OH

O

Cl

SOCl

2

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47

O

Cl

excess NH

3

O

NH

3

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48

22.53
)

a)

O

OH

OH

SOCl

2

O

Cl

OH

b)

O

Cl

NH

excess

O

N

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49

c
)

d
)

CN

CH

3

CH

2

CH

2

MgBr

H

2

O

O

CH

2

CH

2

CH

3

O

OH

OH

O

O

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50

e)

H

N

O

H

2

O

NaOH

NH

2

f)

O

O

O

H

3

O

+

O

O

OH

OH

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51

g)

h
)

Br

NaCN

H

2

O, NaOH

O

O

O

OH

SOCl

2

CH

3

CH

2

CH

2

CH

2

NH

2

LiAlH

4

H

2

O

HN

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52

i)

j)

CN

H

3

O

+

C

O

OH

O

OH

O

HO

heat

O

O

O

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53

k
)

l
)

O

O

O

NH

2

H

N

O

O

O

H

2

O

NaOH

O

O

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54

22.54)

Br

NaCN

CN

H

3

O

+

O

HO

SOCl2

O

Cl

(CH

3

)

2

CuLi

H

2

O

O

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55

CN

LiAlH

4

H

2

O

NH

2

(CH

3

CO)

2

O

NH

O

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56

O

HO

CH

3

OH

H

+

O

O

DIBAL-H

H

2

O

O

CH

3

Li

H

2

O

OH

PCC

O

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57

O

O

LiAlH

4

H

2

O

OH

TsOH

pyridine

OTs

NaCN

CN

CH

3

MgBr

H

2

O

O


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