2.222 – introductory organic chemistry ii – term test...

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NAME: STUDENT NUMBER: Page 1 of 7 University of Manitoba Department of Chemistry 2.222 – Introductory Organic Chemistry II – Term Test 2 Thursday March 20, 2003 This is a 2-hour test, marked out of 50 points total. Part marks are available on all questions. Put all answers in the spaces provided. If more space is required you may use the backs of the exam pages but be sure to indicate that you have done so. A table of spectroscopic data is attached at the end of the exam. 1. (6 MARKS) Provide a detailed stepwise mechanism for the following reaction. O COOEt O O K O O EtOOC THF (H 3 O + workup)

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NAME: STUDENT NUMBER: Page 1 of 7

University of Manitoba Department of Chemistry

2.222 – Introductory Organic Chemistry II – Term Test 2 Thursday March 20, 2003

This is a 2-hour test, marked out of 50 points total. Part marks are available on all questions.

Put all answers in the spaces provided. If more space is required you may use the backs of the exam pages but be sure to indicate that you have done so. A table of spectroscopic data is attached at the end of the exam.

1. (6 MARKS) Provide a detailed stepwise mechanism for the following reaction.

O

COOEt

O

O K

OO

EtOOC

THF

(H3O+ workup)

Page 2 of 7

2. (10 MARKS) Write a stepwise mechanism explaining both steps involved in the formation of a peptide (amide) bond between a carboxylic acid and an amine using the reagent dicyclohexylcarbodiimide, as shown below:

C NN C6H11C6H11

CH2Cl2R OH

OR'H2N

R O

O

NH

NC6H11

C6H11

R NH

R'

O

NH

NH

O

C6H11C6H11

+

Page 3 of 7

3. (5 MARKS) The Meerwein-Ponndorf-Verley Reaction is closely related to one of the reactions in Chapter 12 of our textbook. In this process, a ketone is reduced to a secondary alcohol using an excess of aluminum tri(isopropoxide). Suggest a mechanism for this reaction.

O

+ Al

O

O O

H3C CH3

CH3

CH3

H3C

CH3

H

H

HHO H

+O

(after aqueous acid workup)

Page 4 of 7

4. (10 MARKS) The following multi-step sequence is missing some information. Fill in the blanks with the necessary structure or reagent/solvent to correctly complete the synthesis.

O

O

OHH

H

H2 (g)Pd/CEtOH

p-toluenesulfonic

acid (cat.)

toluene, 80 oC

NaOHH2O

C6H12O

reagent, solvent, workup

Page 5 of 7

5. (14 MARKS) Provide the necessary product, reagent/solvent or starting material to correctly complete each of the following reactions. You may assume that reactions are followed by an aqueous workup procedure if necessary. Mechanisms are NOT required.

a.

O

H

1) NH3Cl, KCN EtOH, reflux

2) aq. H2SO4, reflux

b.

O O

c.

Br

1) Ph3P, EtOH

2) n-BuLi, THF then add

O

H

d.

O

O NaOEtEtOH, reflux

e.

O O

f.

COOH

1)

2)

Page 6 of 7

6. (5 MARKS) You have been presented with a sample of a liquid for structural analysis. It has a pepperminty odour, and is slightly water soluble. Mass spectrometry suggests a molecular weight of 138. The compound has the IR, 13C and 1H NMR spectra shown below. You also perform some chemical tests: • It slowly decolourizes bromine water; • It gives a negative iodoform test; • After sodium fusion, it tests negative with Prussian Blue and also with silver nitrate.

What is the structure of the unknown material?

4 0 0 0 3 0 0 0 2 0 0 0 1 5 0 0 1 0 0 0 5 0 0

NB: This signal is actually 2 very close singlets!

Structure of unknown sample is:

Spectroscopy “Crib Sheet” for 2.222 – Introductory Organic Chemistry II 1H NMR – Typical Chemical Shift Ranges

Type of Proton Chemical Shift (δ) Type of Proton Chemical Shift (δ)

C CH3 0.7 – 1.3 C C H 2.5 – 3.1

C CH2 C 1.2 – 1.4 O

H 9.5 – 10.0

C H

C

C

C

1.4 – 1.7 O

OH

10.0 – 12.0 (solvent dependent)

C H

1.5 – 2.5 C OH

1.0 – 6.0 (solvent dependent)

O

H

2.1 – 2.6 CO H

3.3 – 4.0

Aryl C H 2.2 – 2.7 CCl H

3.0 – 4.0

H 4.5 – 6.5 CBr H

2.5 – 4.0

Aryl H 6.0 – 9.0 CI H

2.0 – 4.0

13C NMR – Typical Chemical Shift Ranges

IR – Typical Functional Group Absorption Bands Group Frequency

(cm-1) Intensity Group Frequency (cm-1) Intensity

C–H 2960 – 2850 Medium RO–H 3650 – 3400 Strong, broad C=C–H 3100 – 3020 Medium C–O 1150 – 1050 Strong C=C 1680 – 1620 Medium C=O 1780 – 1640 Strong C≡C–H 3350 – 3300 Strong R2N–H 3500 – 3300 Medium, broad R–C≡C–R′ 2260 – 2100 Medium (R ≠ R′) C–N 1230, 1030 Medium Aryl–H 3030 – 3000 Medium C≡N 2260 – 2210 Medium Aryl C=C 1600, 1500 Strong RNO2 1540 Strong

12 11 10 9 8 7 6 5 4 3 2 1 0

←δ

R3C–H Aliphatic, alicyclic

X–C–H X = O, N, S, halide

Y

HH

Aromatic, heteroaromatic

Y

H

RCO2H

Y = O, NR, S Y = O, NR, S

“Low Field” “High Field”

220 200 180 160 140 120 100 80 60 40 20 0

←δ

CH3-CR3 CHx-C=O

CR3-CH2-CR3

CHx-Y Y = O, N Alkene

Aryl

Amide Ester Ketone, Aldehyde

Acid

ANSWER KEY Page 1 of 7

University of Manitoba Department of Chemistry

2.222 – Introductory Organic Chemistry II – Term Test 2 Thursday March 20, 2003

This is a 2-hour test, marked out of 50 points total. Part marks are available on all questions.

Put all answers in the spaces provided. If more space is required you may use the backs of the exam pages but be sure to indicate that you have done so. A table of spectroscopic data is attached at the end of the exam.

1. (6 MARKS) Provide a detailed stepwise mechanism for the following reaction.

O

COOEt

O

O K

OO

EtOOC

THF

(H3O+ workup)

O

COOEt

O

H OtBu

O

COOEt

O

COOEt

O

O

12

345

O

OEt

O

O

H3O+duringworkup

OO

EtOOC H

C

BC

This is an aldol followed by a retro-aldol. Notice that the collapse of the alkoxide expels an enolate. The cleavage of a C-C bond is possiblebecause the enolate is a relatively stable anion. This problem is Groutas # 61.

A

BA

1 2

34

5

ANSWER KEY Page 2 of 7

2. (10 MARKS) Write a stepwise mechanism explaining both steps involved in the formation of a peptide (amide) bond between a carboxylic acid and an amine using the reagent dicyclohexylcarbodiimide, as shown below:

3.

C NN C6H11C6H11

CH2Cl2R OH

OR'H2N

R O

O

NH

NC6H11

C6H11

R NH

R'

O

NH

NH

O

C6H11C6H11

+

R OH

O

C

N

N

C6H11

C6H11

R O

O

CN

N

C6H11

C6H11

HR O

O

CNH

N

C6H11

C6H11

R'H2N

RO

O

CNH

N

C6H11

C6H11

NR'H H

RO

OH

CNH

N

C6H11

C6H11

NR'H

R

OH

NR'

HO

CNH

N

C6H11

C6H11

R

O

NR'

HO

CNH

HN

C6H11

C6H11

Several variations on this basic mechanism are possible. A particularly good variation is to use the carboxylic acid to protonate the carbodiimide in the very first step, and then attackwith the resulting carboxylate. This can avoid separation of charge.

This reaction is on page 18-20. Note that the intermediate structure is actually similar to an acid anhydride in many respects, and thus creates a good leaving group for displacement by the amine.

ANSWER KEY Page 3 of 7

(5 MARKS) The Meerwein-Ponndorf-Verley Reaction is closely related to one of the reactions in Chapter 12 of our textbook. In this process, a ketone is reduced to a secondary alcohol using an excess of aluminum tri(isopropoxide). Suggest a mechanism for this reaction.

O

+ Al

O

O O

H3C CH3

CH3

CH3

H3C

CH3

H

H

HHO H

+O

(after aqueous acid workup)

O

Al

O

O O

H3C CH3

R

R

H

+

OAl

OO

OCH3

CH3

RR

H

OAl

OO

O

CH3H3C

RR

H

Acidworkup

HO H

+O

( plus Al2O3 etc)

This reaction is similar to the Cannizzaro Reaction (pp 607-8) and also tothe material in Exercise 12.27 (p 639).

ANSWER KEY Page 4 of 7

4. (10 MARKS) The following multi-step sequence is missing some information. Fill in the blanks with the necessary structure or reagent/solvent to correctly complete the synthesis.

O

O

OHH

H

H2 (g)Pd/CEtOH

p-toluenesulfonic

acid (cat.)

toluene, 80 oC

NaOHH2O

C8H12O

reagent, solvent, workup

O3, CH2Cl2thenZn/HOAc

O

12

34

56

78

12

34

5

678

OH

H

CH3MgBr, Etherthenaq. NH4Cl

H

IntramolecularAldol - from

Exercise 13.7 b

Catalytic Hydrogenation gives syn product

Ozonolysis with

reductive workup,

or KMnO4, H3O+, heat

Grignard addition to ketone

Acid-catalyzedelimination

H

H CH3

This structure (or the ortho isomer), arising from Friedel-Crafts reaction with toluene, is mechanistically reasonable and will also receive full marks in the last step.

ANSWER KEY Page 5 of 7

5. (14 MARKS) Provide the necessary product, reagent/solvent or starting material to correctly complete each of the following reactions. You may assume that reactions are followed by an aqueous workup procedure if necessary. Mechanisms are NOT required.

a.

O

H

1) NH4Cl, KCN EtOH, reflux

2) aq. H2SO4, reflux

NH2

COOH

b.

O OH2Pd or Pt catalystMeOH or other alcohol solvent

c.

Br

1) Ph3P, EtOH

2) n-BuLi, THF then add

O

H

H

d.

O

O NaOEtEtOH, reflux

O

e.

O O

LDA, THF, -78 oC

then Br

f.

COOH

1) AcC l, A lC l3, CH2C l2

2) KM nO 4, heat

NB: You could also have used 1) B r2, FeBr3; 2) Mg/Ether then CO 2

In step 1) you could have alky lated w ith any alkyl halide, sincethese would be oxidized to the ac id as well. The acylation is the better choice because it deactivates the ring towards further reaction, but e ither w ill rece ive fu ll m arks here.

hultin
Note that in the first answer key, there was an extra CH2 group shown for this product.

ANSWER KEY Page 6 of 7

6. (5 MARKS) You have been presented with a sample of a liquid for structural analysis. It has a pepperminty odour, and is slightly water soluble. Mass spectrometry suggests a molecular weight of 138. The compound has the IR, 13C and 1H NMR spectra shown below. You also perform some chemical tests: • It slowly decolourizes bromine water; • It gives a negative iodoform test; • After sodium fusion, it tests negative with Prussian Blue and also with silver nitrate.

What is the structure of the unknown material?

4 0 0 0 3 0 0 0 2 0 0 0 1 5 0 0 1 0 0 0 5 0 0

Structure of unknown sample is:

NB: This signal is actually 2 very close singlets!

O

Isophorone

C9H14OMol. Wt.: 138.21

O O

A BAlthough structures A and B are not correct, they

are both similar enough to the actual structure

that they will also be given full marks. Please

note, however that structure B would NOT

produce a 1H NMR spectrum that was entirely

singlets since the vinylic H would be coupled to

the adjacent CH2.

Spectroscopy “Crib Sheet” for 2.222 – Introductory Organic Chemistry II 1H NMR – Typical Chemical Shift Ranges

Type of Proton Chemical Shift (δ) Type of Proton Chemical Shift (δ)

C CH3 0.7 – 1.3 C C H 2.5 – 3.1

C CH2 C 1.2 – 1.4 O

H 9.5 – 10.0

C H

C

C

C

1.4 – 1.7 O

OH

10.0 – 12.0 (solvent dependent)

C H

1.5 – 2.5 C OH

1.0 – 6.0 (solvent dependent)

O

H

2.1 – 2.6 CO H

3.3 – 4.0

Aryl C H 2.2 – 2.7 CCl H

3.0 – 4.0

H 4.5 – 6.5 CBr H

2.5 – 4.0

Aryl H 6.0 – 9.0 CI H

2.0 – 4.0

13C NMR – Typical Chemical Shift Ranges

IR – Typical Functional Group Absorption Bands Group Frequency

(cm-1) Intensity Group Frequency (cm-1) Intensity

C–H 2960 – 2850 Medium RO–H 3650 – 3400 Strong, broad C=C–H 3100 – 3020 Medium C–O 1150 – 1050 Strong C=C 1680 – 1620 Medium C=O 1780 – 1640 Strong C≡C–H 3350 – 3300 Strong R2N–H 3500 – 3300 Medium, broad R–C≡C–R′ 2260 – 2100 Medium (R ≠ R′) C–N 1230, 1030 Medium Aryl–H 3030 – 3000 Medium C≡N 2260 – 2210 Medium Aryl C=C 1600, 1500 Strong RNO2 1540 Strong

12 11 10 9 8 7 6 5 4 3 2 1 0

←δ

R3C–H Aliphatic, alicyclic

X–C–H X = O, N, S, halide

Y

HH

Aromatic, heteroaromatic

Y

H

RCO2H

Y = O, NR, S Y = O, NR, S

“Low Field” “High Field”

220 200 180 160 140 120 100 80 60 40 20 0

←δ

CH3-CR3 CHx-C=O

CR3-CH2-CR3

CHx-Y Y = O, N Alkene

Aryl

Amide Ester Ketone, Aldehyde

Acid