Organic Chemistry I Exam 4 20101 Name KEY

Multiple Choice - Circle the letter of the best choice for the answer to the question. (2 1/3 Points each) 1. The correct IUPAC name for the following compound is:
Br

A) 2-Bromo-4-methylenehexane C) E) 2-(2-Bromopropyl)-1-butene 4-Bromo-2-ethyl-1-pentene

B) 2-Bromo-4-ethyl-1-pentene D) 2-Bromo-4-ethyl-4-pentene

2.

Give the IUPAC name for

A) 3-Methyl-4-hexyne C) E) 4-Methyl-2-hexyne 2-Ethyl-3-pentyne

B) 4-Ethyl-2-pentyne D) 3-Methyl-2-hexyne

3.

The correct IUPAC name for the following compound is:

Br

A) (E)-2-Bromo-3-chloro-5-methyl-2hexene C) (E)-2-Bromo-3-chloro-5-methyl-3hexene E) (Z)-2-Bromo-3-chloro-5-methyl-3hexene

B) (Z)-2-Bromo-3-chloro-5-methyl-2hexene D) (E)-2-Methyl-5-bromo-4-chloro-4hexene

4.

What is the correct IUPAC name for the following compound?

A) 4-isopropyl-3,4-dimethyl-2-butanol C) E) 2,3,4-trimethyl-4-pentanol 1,1,2,3-tetramethyl-4-pentanol

B) 3,4,5-trimethyl-2-hexanol D) 3,4,5,5-tetramethyl-2-pentanol

5.

Methyl tert-butyl ether has the IUPAC name:

A) methyl dimethylethyl ether C) E) methyoxy-t-butane 2-methoxy-2-methylpropane

B) t-butoxymethane D) 1,1-dimethyl-1methoxyethane

6.

Which of the following carbocations would NOT be likely to undergo rearrangement? A) C)

CH3CHCHCH3 CH3 CH3

B) D)

CH3 CH3CHCH2 CH3

CH3CCHCH2CH3 CH3

E)

CH3 CH3CCH2CH3

7.

What would be the major product of the following reaction?

Cl Cl

Cl Cl

I
Cl

II
Cl

III

IV

A) I C) E) III V

B) II D) IV

8.

The reaction of Br2/CCl4 to cyclohexene would produce the compound(s) represented by structure(s):
H H Br Br Br H H Br Br H Br H

I
A) I alone C) E) III alone II and III (enantiomers)

II

III
B) II alone D) I , II and II

9.

What product would result from the following reaction?

CO2H O K MnO4 OH OH

II

III

OH OH

OH OH

IV

A) I C) E) III V

B) II D) IV

10.

Select the structure of the major product formed in the following reaction.

2 HCl
Cl Cl

Cl Cl

I
Cl Cl

II
Cl Cl

III

IV
A) I C) E) III V

V
B) II D) IV

11.

Which of these is not formed when cyclopentene reacts with an aqueous solution of bromine (Br2 in H2O)?
Br OH Br OH Br Br Br Br OH OH

II

III

IV

A) I C) E) III V

B) II D) IV

12.

How many compounds are possible from the addition of bromine to CH2=CHCH2CH3 (counting stereoisomers separately)? A) One C) E) Three Five B) Two D) Four

13.

In general, when the addition of an unsymmetrical electrophilic reagent to an unsymmetrical alkene forms the product predicted by Markovnikov's rule, that occurs because: A) the product is statistically favored. C) E) steric hindrance favors its formation. All of the above are reasons. B) it is the more/most stable product. D) it is formed via the more/most stable carbocation.

14.

Which of these compounds belongs to the class of substances commonly known as "halohydrins"? A) BrCH2CH2Cl C) E) ClCH2CO2H ICH2CH2OH B) FCH2CH2NH2 D) HOCH2 COCl

15.

The most resistant compound to the action of hot alkaline KMnO4 is: A) Pentane C) E) 1-Pentene 2-Pentene B) 2-Pentyne D) Cyclopentene

16.

Consider the ozonolysis products obtained from all the unbranched and unsymmetrical isomers of heptene. The reaction product in each case would consist of: A) a single aldehyde. C) E) an aldehyde and a ketone. two different ketones. B) two different aldehydes. D) a single ketone.

17.

In the presence of light, ethane (1 mol) reacts with chlorine (1 mol) to form which product(s)? A) CH2ClCHCl2 C) E) CH3CHCl2 CH3CH2Cl (one point for this one) B) ClCH2CH2Cl D) All of these

18.

Select the structure of the major product formed in the following reaction.
CH3

Br2 h

?
Br CH3

CH2Br

Br

CH3

CH3 Br

Br

II

III

IV

A) I C) E) III V

B) II D) IV

19.

Which of the following combinations of reactants can provide a demonstrable example of anti-Markovnikov addition? A) CH2=CHCH3 + HCl + ROOR C) E) CH3CH=CH2 + H2O + Cl2 CH3CH=CHCH3 + HBr + ROOR B) CH3CH2CH=CH2 + HBr + ROOR D) CH3CH2CH=CH2 + Br2 + ROOR

20.

What sequence of reactions could be used to prepare cis-1,2-cyclopentanediol from cyclopentane? (1) Cl2, h; (2) t-BuOK/t-BuOH; (3) OsO4; (4) NaHSO3/H2O (1) t-BuOK/t-BuOH; (2) Cl2, h; (3) NaOH/H2O (1) Cl2, h; (2) t-BuOK/t-BuOH; (3) H2O2 (1) NaOH/H2O; (2) Br2; (3) NaNH2(2eq.)/liq.NH3; (4) KMnO4, NaOH/H2O, 5C E) (1) Cl2, h; (2) t-BuOK/t-BuOH; (3) Hg(OAc)2, H2O (4) NaBH4, H3O+ A) B) C) D)

21.

The p-orbital of a methyl radical carbon, CH3, contains how many electrons? A) 1 C) E) 3 0 B) 2 D) 4

22.

Which of the following free radicals is the most stable? A)

B)

CH3 CH3CHCHCH3

C)

CH3 CH3CHCH2CH2

D)

CH3 CH3CCH2CH3

E)

CH3 CH2CHCH2CH3

23.

Free radicals can be produced by: A) use of high temperatures. C) E) irradiation with light. all of A), B) and C). B) reaction of a molecule with another free radical. D) both A) and B).

24.

What is the final product, C, obtained via the following reaction sequence?
Br2 h A t-BuOK t-BuOH heat
OH

i) BH3, THF ii) H2O2, OH

OH

OH

OH

OH OH

II

III

IV

A) I C) E) III V

B) II D) IV

25.

Which of the following reactions would serve as a synthesis of butyl bromide? A)

B) CH CH CH CH OH + PBr 3 2 2 2 3 reflux C) CH3CH2CH2CH2OH + NaBr D) CH CH CH CH OH + Br 3 2 2 2 2 E) Answers A) and B) only (one point for A or B)

26.

The product(s) of the following reaction

excess HBr
CH2

heat

is/are:

CH3CH2OCH2CH3 I

CH3CH2CH2CH2OH and CH3CH2CH2CH2Br II

BrCH2CH2CH2CH2OH and BrCH2CH2CH2CH2Br III

CH2

IV

27.

Which product(s) would you expect to obtain from the following sequence of reactions?
CH3

1. BH3-THF 2. H2O2, NaOH

?
H3C O

CH3 CH3 OH OH

CH3 OH

CH2OH

+ enantiomer I II

+ enantiomer III

+ enantiomer IV V

A) I C) E) III (Syn addition of H and OH) V

B) II D) IV

28.

Select the structure of the major product formed from the following reaction.
CH3

1. Hg(OOCCH3)2 THF, H2O 2. NaBH4, NaOH

CH3 OH

CH3

CH2OH

HO CH3

CH3

OH OH

II

III

IV

A) I C) E) III V

B) II D) IV

29.

Which is the best way to prepare 3-methoxypentane via the Williamson method? (Hint - Draw the structure of the product first.) A) B) C) D) E) CH3OH + CH3CH2CHOHCH2CH3 + H2SO4, 140C CH3OH + (CH3)2CHCH2CH2OH + H2SO4, 140C CH3ONa + (CH3CH2)2CHBr (Mostly E2) CH3I + (CH3CH2)2CHONa CH3I + (CH3)2CHCH2CH2ONa

30.

Epoxidation followed by reaction with aqueous base converts cyclopentene into which of these?
H OH H H OH OH H OH OH H H H OH OH

II

III

IV

A) I C) III

B) II D) IV

E)

Equal amounts of III and IV

(III and IV are enantiomers)

31.

What would be the final product?

product

CH3OH, HA

final product

A) (CH3)2CHCH2OCH3 B) (CH3)2CCH3
OCH3

C) (CH3)2CCH2OH (the nucleophile attacks the most sub. C in acidic conditions (HA)) D) (CH3)2CCH2OCH3 E)
OH (CH3)2CCH2OCH3

OCH3

OCH3

32.

What would be the major product of the following reaction?

CH3SO2Cl base

mesylate

NaI ethanol

II

III

IV

A) I C) E) III V

B) II (SN2 backside by I- after mes formed from -OH) D) IV

33.

Which of the compounds listed below would you expect to have the highest boiling point? (They all have approximately the same molecular weight.) A) CH3CH2CH2CH2CH3 C) E) CH3CH2CH2CH2OH CH3CH2CH2OCH3 B) CH3CH2CH2Cl D) CH3CH2OCH2CH3

34.

The following reaction,

is probably: A) B) C) D) E) An SN1-type reaction involving the protonated alcohol as the substrate. An SN2-type reaction involving the protonated alcohol as the substrate. An E1-type reaction involving the protonated alcohol as the substrate. An E2-type reaction involving the protonated alcohol as the substrate. An epoxidation reaction.

35.

Which of the following statements is NOT true of ethers? A) Ethers are generally unreactive molecules toward reagents other than certain strong acids. B) Ethers generally have lower boiling points than alcohols of a corresponding molecular weight. C) Ethers cannot H-bond with water. (It can, but not with another ether molecule) D) Ethers can generally be cleaved by heating them with HBr or HI. E) Ethers form peroxides when allowed to stand in the presence of oxygen. (Hint This is true)

36.

Which compound is a tosylate?

I
O CH3 S CH3

II
O CH3 O S O CH3

III

IV

A) I C) E) III V

B) II D) IV

Mechanisms Write the mechanism for the following reaction. Use curved arrow notation and indicate the removal of any protons if necessary. The reaction of 1-methylcyclohexene with HBr followed by the reaction of the product with t-butoxide in t-butyl alcohol at 60Cto make an alkene different from the starting material. (8 Points) Electron "dots" not shown in solutions to make drawing easier. You should have shown them.

CH3 H H Br

CH3 Br H H

CH3 Br

H C Br

H H

O-t-but

CH2

Mechanisms Write the mechanism for the following reaction. Use curved arrow notation and indicate the removal of any protons if necessary. The reaction of ethyl alcohol molecules in the presence of concentrated sulfuric acid at 140 to produce diethyl ether. (8 points)

CH3 CH2 OH H H2SO 4 CH3 CH2 OH CH3 CH2 OH2 CH3 CH2 O CH2 CH3

CH3 CH2 OH

CH3 CH2 O CH2 CH3