Deck 12: Alcohols and Phenols
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Deck 12: Alcohols and Phenols
1
Provide the structure for 6-sec-butyl-7,7-dimethyl-4-decanol.

2
What is the IUPAC name for the following compound? 
A) 2-methyl-5-bromocyclohexanol
B) 3-bromo-2-methylcyclohexanol
C) 1-bromo-4-methylcyclohexanol
D) 4-bromo-6-methylcyclohexanol
E) 4-bromo-2-methylcyclohexanol

A) 2-methyl-5-bromocyclohexanol
B) 3-bromo-2-methylcyclohexanol
C) 1-bromo-4-methylcyclohexanol
D) 4-bromo-6-methylcyclohexanol
E) 4-bromo-2-methylcyclohexanol
4-bromo-2-methylcyclohexanol
3
What is the IUPAC name for the following compound? 

7-ethyl-8-methyl-4-nonanol
4
What is the IUPAC name for the following compound? 

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5
What is the IUPAC name for t-butyl alcohol?
A) 1-butanol
B) 2-methyl-1-propanol
C) 2-methyl-2-propanol
D) 2-butanol
E) 1,1-dimethyl-1-ethanol
A) 1-butanol
B) 2-methyl-1-propanol
C) 2-methyl-2-propanol
D) 2-butanol
E) 1,1-dimethyl-1-ethanol
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6
Provide the structure for 5-chloro-2-propyl-1-heptanol.
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7
What is the correct structure for 1-chloro-3-ethyl-2-pentanol?

A) I
B) II
C) III
D) IV
E) None of these

A) I
B) II
C) III
D) IV
E) None of these
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8
What is the IUPAC name for the following compound? 
A) (R)-3-hexyn-2-ol
B) (S)-3-hexyn-2-ol
C) (R)-2-hexyn-4-ol
D) (S)-2-hexyn-4-ol
E) (S)-2-hydroxy-3-hexyne

A) (R)-3-hexyn-2-ol
B) (S)-3-hexyn-2-ol
C) (R)-2-hexyn-4-ol
D) (S)-2-hexyn-4-ol
E) (S)-2-hydroxy-3-hexyne
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9
What is the correct structure for 2,2-dibromo-1-methylcyclohexanol? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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10
What is the IUPAC name for the following compound? 
A) 4-isopropyl-3,4-dimethyl-2-butanol
B) 2,3,4-trimethyl-4-pentanol
C) 1,1,2,3-tetramethyl-4-pentanol
D) 3,4,5-trimethyl-2-hexanol
E) 3,4,5,5-tetramethyl-2-pentanol

A) 4-isopropyl-3,4-dimethyl-2-butanol
B) 2,3,4-trimethyl-4-pentanol
C) 1,1,2,3-tetramethyl-4-pentanol
D) 3,4,5-trimethyl-2-hexanol
E) 3,4,5,5-tetramethyl-2-pentanol
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11
What is the IUPAC name for the following compound? 
A) 3-methyl-4-ethyl-3-hexen-6-ol
B) 4-ethyl-3-methyl-3,6-hexenol
C) 3-ethyl-4-methyl-3-hexen-1-ol
D) 3-methyl-4-(2-hydroxyethyl)-3-hexene
E) 3-(2-hydroxyethyl)-3-methyl-3-hexene

A) 3-methyl-4-ethyl-3-hexen-6-ol
B) 4-ethyl-3-methyl-3,6-hexenol
C) 3-ethyl-4-methyl-3-hexen-1-ol
D) 3-methyl-4-(2-hydroxyethyl)-3-hexene
E) 3-(2-hydroxyethyl)-3-methyl-3-hexene
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12
Give the structure for (E)-4,5,5-trimethyl-3-hepten-1-ol.
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13
What is the IUPAC name for the following compound? 
A) 4-penten-2-methyl-2-ol
B) 4-methyl-1-penten-2-ol
C) 2-methyl-4-penten-2-ol
D) 4-methyl-1-penten-4-ol
E) 4-hydroxy-4-methyl-1-pentene

A) 4-penten-2-methyl-2-ol
B) 4-methyl-1-penten-2-ol
C) 2-methyl-4-penten-2-ol
D) 4-methyl-1-penten-4-ol
E) 4-hydroxy-4-methyl-1-pentene
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14
What is the IUPAC name for the following compound? 
A) 1,1,1-triethylmethanol
B) 1,1-diethyl-1-propanol
C) 2-ethyl-3-pentanol
D) 3-ethyl-3-pentanol
E) t-heptanol

A) 1,1,1-triethylmethanol
B) 1,1-diethyl-1-propanol
C) 2-ethyl-3-pentanol
D) 3-ethyl-3-pentanol
E) t-heptanol
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15
What is the IUPAC name for isobutyl alcohol?
A) 2-methyl-1-propanol
B) 2-methyl-1-butanol
C) 1-methyl-1-propanol
D) 1,1-dimethyl-1-ethanol
E) 3-methyl-1-propanol
A) 2-methyl-1-propanol
B) 2-methyl-1-butanol
C) 1-methyl-1-propanol
D) 1,1-dimethyl-1-ethanol
E) 3-methyl-1-propanol
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16
What is the correct structure for (E)-5,5-dimethyl-3-hepten-1-ol? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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17
What is the IUPAC name for the following compound? 

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18
What is the IUPAC name for the following compound? 
A) 1-isopropyl-4-cyclopentanol
B) 3-isopropylcyclopentanol
C) 1-isopropyl-3-cyclopentanol
D) 1-isopropyl-4-hydroxycyclopentane
E) None of these

A) 1-isopropyl-4-cyclopentanol
B) 3-isopropylcyclopentanol
C) 1-isopropyl-3-cyclopentanol
D) 1-isopropyl-4-hydroxycyclopentane
E) None of these
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19
What is the IUPAC name for the following compound? 

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20
What is the IUPAC name for the following compound? 

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21
What is the IUPAC name for the following compound? 

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22
What is the IUPAC name for the following compound? 

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23
What is the IUPAC name for the following compound? 
A) cis-1,2-cyclopentanediol
B) meso-1,2-cyclopentanediol
C) (1R,2R)-1,2-cyclopentanediol
D) (1R,2S)-1,2-cyclopentanediol
E) (1S,2S)-1,2-cyclopentanediol

A) cis-1,2-cyclopentanediol
B) meso-1,2-cyclopentanediol
C) (1R,2R)-1,2-cyclopentanediol
D) (1R,2S)-1,2-cyclopentanediol
E) (1S,2S)-1,2-cyclopentanediol
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24
Identify the alcohol in alcoholic drinks.
A) methanol
B) 2-propanol
C) ethanol
D) 1-butanol
E) 1-propanol
A) methanol
B) 2-propanol
C) ethanol
D) 1-butanol
E) 1-propanol
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25
Identify wood alcohol.
A) methanol
B) 2-propanol
C) ethanol
D) 1-butanol
E) 1-propanol
A) methanol
B) 2-propanol
C) ethanol
D) 1-butanol
E) 1-propanol
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26
Identify rubbing alcohol.
A) methanol
B) 2-propanol
C) ethanol
D) 1-butanol
E) 1-propanol
A) methanol
B) 2-propanol
C) ethanol
D) 1-butanol
E) 1-propanol
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27
Rank the following alcohols in decreasing order of acidity. Explain your answer.
A) II > I > III
B)I > II > III
C)I > III > II
D)III > I > II
E) III > II > I
A) II > I > III
B)I > II > III
C)I > III > II
D)III > I > II
E) III > II > I
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28
What is the IUPAC name for the following compound? HOCH2CH2CH2OH
A) 1,2-butanediol
B) isopropyl alcohol
C) 1-propanol
D) 1,3-propanediol
E) 1,2-ethanediol
A) 1,2-butanediol
B) isopropyl alcohol
C) 1-propanol
D) 1,3-propanediol
E) 1,2-ethanediol
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29
Explain why cyclohexanol has a pKa of 18 and phenol has a pKa of 10. Use structural drawings to explain your reasoning.
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30
What is the correct structure for 2-methylphenol? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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31
What is the IUPAC name for the following compound? 
A) 3,4-dibromophenol
B) 2,4-dibromophenol
C) 2,5-dibromophenol
D) 3,6-dibromophenol
E) 2,6-dibromophenol

A) 3,4-dibromophenol
B) 2,4-dibromophenol
C) 2,5-dibromophenol
D) 3,6-dibromophenol
E) 2,6-dibromophenol
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32
What is the IUPAC name for the following compound? 

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33
Identify the type of bonding between molecules of alcohol.
A) ion-ion
B) van der Waals forces
C) hydrogen bonding
D) ion-dipole
E) London dispersion
A) ion-ion
B) van der Waals forces
C) hydrogen bonding
D) ion-dipole
E) London dispersion
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34
What is the correct structure for 2-bromo-5-isopropylphenol? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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35
Rank the following alcohols in decreasing order of acidity. 
A) II > I > III
B) I > II > III
C) I > III > II
D) III > I > II
E) III > II > I

A) II > I > III
B) I > II > III
C) I > III > II
D) III > I > II
E) III > II > I
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36
What is the IUPAC name for the following compound? 

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37
Provide the structure for (2R,3S) -2-bromo-1,3-pentanediol.
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38
Identify grain alcohol.
A) methanol
B) 2-propanol
C) ethanol
D) 1-butanol
E) 1-propanol
A) methanol
B) 2-propanol
C) ethanol
D) 1-butanol
E) 1-propanol
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39
What is the IUPAC name for the following compound? 

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40
Which one of the following alcohols is most acidic? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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41
Identify the characteristics of the acid-catalyzed hydration of an alkene.
A) Markovnikov, with rearrangement possible
B) Markovnikov, with no rearrangement possible
C) anti-Markovnikov, with rearrangement possible
D) anti-Markovnikov, with no rearrangement possible
A) Markovnikov, with rearrangement possible
B) Markovnikov, with no rearrangement possible
C) anti-Markovnikov, with rearrangement possible
D) anti-Markovnikov, with no rearrangement possible
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42
Predict the product(s) for the following reaction. 

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43
Provide the reagents necessary to carry out the following conversion. 

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44
Predict the product for the following reaction.

A) I
B) II
C) III
D) IV
E) None of these

A) I
B) II
C) III
D) IV
E) None of these
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45
Predict the product(s) for the following reaction. 

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46
What are the oxidation states of carbon atoms I and II in the following reaction? 
A) I. +1, II. +2
B) I. +2, II. +2
C) I. +1, II. +3
D) I. +3, II. +2
E) I. +2, II. +1

A) I. +1, II. +2
B) I. +2, II. +2
C) I. +1, II. +3
D) I. +3, II. +2
E) I. +2, II. +1
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47
For the following conversion, identify if the starting material has been oxidized, reduced or neither. Explain your answer. 

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48
For the following conversion, identify if the starting material has been oxidized, reduced or neither. Explain your answer. 

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49
Identify the characteristics of the hydroboration-oxidation of an alkene.
A) Markovnikov, with rearrangement possible
B) Markovnikov, with no rearrangement possible
C) anti-Markovnikov, with rearrangement possible
D) anti-Markovnikov, with no rearrangement possible
A) Markovnikov, with rearrangement possible
B) Markovnikov, with no rearrangement possible
C) anti-Markovnikov, with rearrangement possible
D) anti-Markovnikov, with no rearrangement possible
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50
Predict the major product for the following reaction. 

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51
Provide the reagents necessary to carry out the following conversion. 

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52
Identify the characteristics of the oxymercuration-demercuration of an alkene.
A) Markovnikov, with rearrangement possible
B) Markovnikov, with no rearrangement possible
C) anti-Markovnikov, with rearrangement possible
D) anti-Markovnikov, with no rearrangement possible
A) Markovnikov, with rearrangement possible
B) Markovnikov, with no rearrangement possible
C) anti-Markovnikov, with rearrangement possible
D) anti-Markovnikov, with no rearrangement possible
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53
Provide the reagents necessary to carry out the following conversion. 
A) NaOH/H2O
B) 1. NaOCH3, 2. H3O+
C) 1. (CH3)3COK, 2. BH3•THF, 3. H2O2/NaOH/H2O
D) 1. (CH3)3COK, 2. H3O+
E) B & D

A) NaOH/H2O
B) 1. NaOCH3, 2. H3O+
C) 1. (CH3)3COK, 2. BH3•THF, 3. H2O2/NaOH/H2O
D) 1. (CH3)3COK, 2. H3O+
E) B & D
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54
Provide the reagents necessary to carry out the following conversion. 

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55
Predict the product for the following reaction. 

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56
Rank the following alcohols in decreasing order of acidity. 
A) II > I > III
B) I > II > III
C) I > III > II
D) III > I > II
E) III > II > I

A) II > I > III
B) I > II > III
C) I > III > II
D) III > I > II
E) III > II > I
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57
Predict the product(s) for the following reaction.

A) I
B) II
C) III
D) IV
E) None of these

A) I
B) II
C) III
D) IV
E) None of these
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58
Predict the product for the following reaction.

A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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59
For the following conversion, identify if the starting material has been oxidized, reduced or neither. 

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60
What are the oxidation states of carbon atoms I and II in the following compound? 
A) I. +1, II. +2
B) I. +2, II. +2
C) I. +1, II. +3
D) I. +3, II. +2
E) I. +2, II. +1

A) I. +1, II. +2
B) I. +2, II. +2
C) I. +1, II. +3
D) I. +3, II. +2
E) I. +2, II. +1
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61
Predict the product(s) for the following reaction. 

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62
Predict the product for the following reaction. 

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63
Provide the reagents necessary to carry out the following conversion. 
A) KMnO4, NaOH,H2O
B) KMnO4, H3O+, 75oC
C) H2SO4, heat
D) 1. mCPBA 2. H3O+
E) none of these

A) KMnO4, NaOH,H2O
B) KMnO4, H3O+, 75oC
C) H2SO4, heat
D) 1. mCPBA 2. H3O+
E) none of these
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64
Predict the product(s) for the following reaction.

A) I
B) II
C) III
D) IV
E) none of these

A) I
B) II
C) III
D) IV
E) none of these
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65
Predict the product for the following reaction.

A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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66
Provide the reagents necessary to carry out the following conversion. 
A) KMnO4, NaOH,H2O,cold
B) KMnO4, H3O+, 75oC
C) H2SO4, heat
D) 1. mCPBA 2. H3O+
E) none of these

A) KMnO4, NaOH,H2O,cold
B) KMnO4, H3O+, 75oC
C) H2SO4, heat
D) 1. mCPBA 2. H3O+
E) none of these
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67
Predict the product for the following reaction. 

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68
Provide the reagent(s) necessary to carry out the following conversion. 

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69
For the following conversion, identify if the starting material has been oxidized, reduced or neither. 
A) reduced
B) oxidized
C) neither
D) A & B

A) reduced
B) oxidized
C) neither
D) A & B
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70
For the following conversion, identify if the starting material has been oxidized, reduced or neither. 
A) reduced
B) oxidized
C) neither
D) A & B

A) reduced
B) oxidized
C) neither
D) A & B
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71
Predict the product(s) for the following reaction sequence.

A) I
B) II
C) III
D) Both I & II
E) None of these

A) I
B) II
C) III
D) Both I & II
E) None of these
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72
Predict the product for the following reaction. 

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73
Predict the product for the following reaction. 

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74
Provide the reactant (A) for the following reaction.

A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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75
Predict the product for the following reaction sequence. 

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76
Predict the product for the following reaction.

A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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77
Provide the structure of each product (A-D) in the following reaction sequence. 

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78
Provide the reagent(s) necessary to carry out the following conversion. 

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79
Predict the product for the following reaction.

A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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80
Which one of the following compounds gives 5-methyl-3-heptanol with LiAlH4 followed by water? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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