Deck 9: Aldehydes and Ketones

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Question
Which of the hydrogens in the following molecule are most acidic? The hydrogens on carbon <strong>Which of the hydrogens in the following molecule are most acidic? The hydrogens on carbon  </strong> A) 1 B) 2 C) 3 D) 4 E) 5 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
E) 5
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Question
What is the structure of cyclohexanecarbaldehyde?

A) <strong>What is the structure of cyclohexanecarbaldehyde?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>What is the structure of cyclohexanecarbaldehyde?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>What is the structure of cyclohexanecarbaldehyde?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>What is the structure of cyclohexanecarbaldehyde?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>What is the structure of cyclohexanecarbaldehyde?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The enol tautomer of 3-pentanone is:

A) <strong>The enol tautomer of 3-pentanone is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>The enol tautomer of 3-pentanone is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>The enol tautomer of 3-pentanone is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>The enol tautomer of 3-pentanone is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>The enol tautomer of 3-pentanone is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What class of compound most closely resembles an acetal in its reactivity with CH3MgBr?

A) ethers
B) aldehydes
C) ketones
D) alcohols
E) thiols
Question
Which of the following compounds is a cyanohydrin?

A) <strong>Which of the following compounds is a cyanohydrin?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following compounds is a cyanohydrin?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following compounds is a cyanohydrin?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following compounds is a cyanohydrin?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following compounds is a cyanohydrin?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following compounds is a hemiacetal?

A) <strong>Which of the following compounds is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following compounds is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following compounds is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following compounds is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following compounds is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The number of a-hydrogens in <strong>The number of a-hydrogens in   is:</strong> A) 1 B) 3 C) 4 D) 8 E) 14 <div style=padding-top: 35px> is:

A) 1
B) 3
C) 4
D) 8
E) 14
Question
Which of the following molecules is a hemiacetal?

A) <strong>Which of the following molecules is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following molecules is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following molecules is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following molecules is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following molecules is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following aldehydes can exist in equilibrium with a cyclic hemiacetal?

A) 4-pentenal
B) 3-hydroxypropanal
C) 2-hydroxybutanal
D) 3-hydroxybutanal
E) 4-hydroxybutanal
Question
The equilibrium that exists between the keto and enol forms of aldehydes and ketones is known as:

A) stereoisomerism
B) configurational isomerism
C) geometric isomerism
D) tautomerism
E) positional isomerism
Question
The name of the following is:
<strong>The name of the following is:   </strong> A) 2-hydroxy-4-pentanone. B) 2-oxo-4-pentanol. C) 4-oxo-2-pentanol. D) 1-acetyl-2-propanol. E) 4-hydroxy-2-pentanone. <div style=padding-top: 35px>

A) 2-hydroxy-4-pentanone.
B) 2-oxo-4-pentanol.
C) 4-oxo-2-pentanol.
D) 1-acetyl-2-propanol.
E) 4-hydroxy-2-pentanone.
Question
The expected order of boiling points of the following is: <strong>The expected order of boiling points of the following is:  </strong> A) 3>2>1 B) 2>1>3 C) 2>3>1 D) 1>2>3 E) 1>3>2 <div style=padding-top: 35px>

A) 3>2>1
B) 2>1>3
C) 2>3>1
D) 1>2>3
E) 1>3>2
Question
The predominant product from the reaction below is: <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A) <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The IUPAC name for ethyl methyl ketone is

A) 2-butanone
B) 2-pentanone
C) 3-pentanone
D) propanone
E) acetophenone
Question
Which of the following molecules has the highest boiling point?

A) o-xylene
B) m-xylene
C) p-xylene
D) benzaldehyde
E) benzyl alcohol
Question
The IUPAC name for the following molecule is: <strong>The IUPAC name for the following molecule is:  </strong> A) 3-ethyl-1-phenyl-3-pentenone B) 3-ethyl-5-phenyl-2-penten-4-one C) allyl benzyl ketone D) (E)-3-ethyl-1-phenyl-3-penten-2-one E) (Z)-3-ethyl-1-phenyl-3-penten-2-one <div style=padding-top: 35px>

A) 3-ethyl-1-phenyl-3-pentenone
B) 3-ethyl-5-phenyl-2-penten-4-one
C) allyl benzyl ketone
D) (E)-3-ethyl-1-phenyl-3-penten-2-one
E) (Z)-3-ethyl-1-phenyl-3-penten-2-one
Question
What is the class of compound produced from the reaction of a ketone with hydrazine?

A) oxime
B) amide
C) hydrazone
D) semicarbazone
E) imide
Question
The common name for the following molecule is: <strong>The common name for the following molecule is:  </strong> A) acetaldehyde B) dimethyl aldehyde C) ethyl ketone D) formaldehyde E) methylmethanal <div style=padding-top: 35px>

A) acetaldehyde
B) dimethyl aldehyde
C) ethyl ketone
D) formaldehyde
E) methylmethanal
Question
Which of the following is a hydrazone?

A) <strong>Which of the following is a hydrazone?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following is a hydrazone?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following is a hydrazone?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following is a hydrazone?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following is a hydrazone?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
In a carbonyl group

A) the oxygen acts as a Lewis acid.
B) the C=O bond length is shortened due to resonance.
C) the carbon is sp3 hybridized.
D) the carbon is nucleophilic and the oxygen is electrophilic.
E) the carbon is electrophilic and the oxygen is nucleophilic.
Question
What type of compound is produced from the following reaction? <strong>What type of compound is produced from the following reaction?  </strong> A) an amide B) an alcohol C) an acid D) an aldehyde E) a ketone <div style=padding-top: 35px>

A) an amide
B) an alcohol
C) an acid
D) an aldehyde
E) a ketone
Question
Which of the following nucleophiles add reversibly to a carbonyl group? <strong>Which of the following nucleophiles add reversibly to a carbonyl group?  </strong> A) I, II and IV B) II C) I and II D) III and IV E) I, II, III and IV <div style=padding-top: 35px>

A) I, II and IV
B) II
C) I and II
D) III and IV
E) I, II, III and IV
Question
Which hydrogens in the following compound will be exchanged most rapidly for deuterium upon reaction with D2O and NaOD? <strong>Which hydrogens in the following compound will be exchanged most rapidly for deuterium upon reaction with D<sub>2</sub>O and NaOD?  </strong> A) H<sub>1</sub> B) H<sub>2</sub> C) H<sub>3</sub> D) H<sub>4</sub> E) H<sub>5</sub> <div style=padding-top: 35px>

A) H1
B) H2
C) H3
D) H4
E) H5
Question
In the mechanism for acid catalyzed hemiacetal formation, the first step is:

A) protonation of the carbonyl oxygen
B) nucleophilic attack at the carbonyl carbon
C) protonation of the oxygen of the alcohol
D) nucleophilic attack at the carbon of the alcohol
E) elimination of a water molecule
Question
Which of the following compounds will not act as a nucleophile in an Aldol reaction?

A) <strong>Which of the following compounds will not act as a nucleophile in an Aldol reaction?</strong> A)   B)   C)   D) HCHO E) C and D <div style=padding-top: 35px>
B) <strong>Which of the following compounds will not act as a nucleophile in an Aldol reaction?</strong> A)   B)   C)   D) HCHO E) C and D <div style=padding-top: 35px>
C) <strong>Which of the following compounds will not act as a nucleophile in an Aldol reaction?</strong> A)   B)   C)   D) HCHO E) C and D <div style=padding-top: 35px>
D) HCHO
E) C and D
Question
What statement is false relative to the nucleophilic additions?

A) When a weak nucleophile is present, the reaction can be catalyzed by acid.
B) The nucleophile attacks the trigonal carbon of the carbonyl group.
C) Ketones are more reactive than aldehydes.
D) Nucleophiles that add irreversibly are poor leaving groups.
E) Nucleophiles can be classified as those that add reversibly to carbonyl compounds and those that add irreversibly.
Question
Which statement about the mechanism of imine formation from a primary amine and an aldehyde or ketone is false?

A) The first steps involve addition of the amine to the carbonyl carbon to form a tetrahedral intermediate.
B) The last steps involve elimination of water to form a carbon-nitrogen p-bond.
C) All steps are reversible.
D) The reaction involves SN2 displacement of the carbonyl oxygen by the amine nitrogen.
E) The reaction does not require a strong acid catalyst.
Question
Which of the following reactions will produce a cyanohydrin?

A) <strong>Which of the following reactions will produce a cyanohydrin?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following reactions will produce a cyanohydrin?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following reactions will produce a cyanohydrin?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following reactions will produce a cyanohydrin?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following reactions will produce a cyanohydrin?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The products from <strong>The products from   are:</strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px> are:

A) <strong>The products from   are:</strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
B) <strong>The products from   are:</strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
C) <strong>The products from   are:</strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
D) <strong>The products from   are:</strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
E) no reaction
Question
Which of the following compounds will give a positive silver mirror test (Tollens' test)?

A) <strong>Which of the following compounds will give a positive silver mirror test (Tollens' test)?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following compounds will give a positive silver mirror test (Tollens' test)?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following compounds will give a positive silver mirror test (Tollens' test)?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following compounds will give a positive silver mirror test (Tollens' test)?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following compounds will give a positive silver mirror test (Tollens' test)?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What is the structure of the aldol produced from reacting propanone with NaOH?

A) <strong>What is the structure of the aldol produced from reacting propanone with NaOH?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>What is the structure of the aldol produced from reacting propanone with NaOH?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>What is the structure of the aldol produced from reacting propanone with NaOH?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>What is the structure of the aldol produced from reacting propanone with NaOH?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>What is the structure of the aldol produced from reacting propanone with NaOH?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The second step in the base catalyzed aldol condensation is:

A) formation of the enolate ion
B) addition of an enolate to a carbonyl group
C) protonation of the alkoxide ion
D) protonation of the carbonyl oxygen
E) loss of a proton from the α\alpha carbon
Question
Which reagent will accomplish the following transformation? <strong>Which reagent will accomplish the following transformation?  </strong> A) NaOH B) CrO<sub>3</sub>, H<sub>2</sub>SO<sub>4</sub> C) CH<sub>3</sub>MgBr D) NaBH<sub>4</sub> E) H<sub>2</sub>, Pd <div style=padding-top: 35px>

A) NaOH
B) CrO3, H2SO4
C) CH3MgBr
D) NaBH4
E) H2, Pd
Question
What reaction will produce the following product? <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A) <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What Grignard reagent and carbonyl compound react to give benzyl alcohol after treatment with aqueous acid?

A) phenyl magnesium bromide and formaldehyde
B) phenyl magnesium bromide and oxirane
C) benzaldehyde and methyl magnesium bromide
D) benzaldehyde and ethyl magnesium chloride
E) acetophenone and methyl magnesium chloride
Question
Which reagents would you use to accomplish the following conversion? <strong>Which reagents would you use to accomplish the following conversion?  </strong> A) NaBH<sub>4</sub>, H<sub>2</sub>O B) LiAlH<sub>4</sub>, ether; then H<sub>3</sub>O<sup>+</sup> C) H<sub>2</sub>, Pt D) all of these E) none of these <div style=padding-top: 35px>

A) NaBH4, H2O
B) LiAlH4, ether; then H3O+
C) H2, Pt
D) all of these
E) none of these
Question
An oxime can be produced by the reaction of an aldehyde and:

A) hydroxylamine
B) hydrazine
C) methylamine
D) phenylhydrazine
E) semicarbazide
Question
The product from <strong>The product from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px> is:

A) <strong>The product from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>The product from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>The product from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>The product from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>The product from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The reaction of a Grignard reagent with acetone followed by acid hydrolysis will produce what type of product?

A) a primary alcohol
B) a secondary alcohol
C) a tertiary alcohol
D) a carboxylic acid
E) a ketone
Question
What reactants give the following molecule upon acid hydrolysis? <strong>What reactants give the following molecule upon acid hydrolysis?  </strong> A) cyclohexyl magnesium bromide and acetaldehyde B) cyclohexanol and   C) cyclohexanone and   D) cyclohexanecarbaldehyde and   E) cyclohexanone and ethenyl magnesium bromide <div style=padding-top: 35px>

A) cyclohexyl magnesium bromide and acetaldehyde
B) cyclohexanol and <strong>What reactants give the following molecule upon acid hydrolysis?  </strong> A) cyclohexyl magnesium bromide and acetaldehyde B) cyclohexanol and   C) cyclohexanone and   D) cyclohexanecarbaldehyde and   E) cyclohexanone and ethenyl magnesium bromide <div style=padding-top: 35px>
C) cyclohexanone and <strong>What reactants give the following molecule upon acid hydrolysis?  </strong> A) cyclohexyl magnesium bromide and acetaldehyde B) cyclohexanol and   C) cyclohexanone and   D) cyclohexanecarbaldehyde and   E) cyclohexanone and ethenyl magnesium bromide <div style=padding-top: 35px>
D) cyclohexanecarbaldehyde and <strong>What reactants give the following molecule upon acid hydrolysis?  </strong> A) cyclohexyl magnesium bromide and acetaldehyde B) cyclohexanol and   C) cyclohexanone and   D) cyclohexanecarbaldehyde and   E) cyclohexanone and ethenyl magnesium bromide <div style=padding-top: 35px>
E) cyclohexanone and ethenyl magnesium bromide
Question
The aldol obtained by treating <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px> with base is:

A) <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The organic product of the reaction <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px> is:

A) <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
How many hydrogens in the following compound will be exchanged for deuterium upon reaction with D2O and an acid catalyst? <strong>How many hydrogens in the following compound will be exchanged for deuterium upon reaction with D<sub>2</sub>O and an acid catalyst?  </strong> A) 0 B) 2 C) 4 D) 5 E) 8 <div style=padding-top: 35px>

A) 0
B) 2
C) 4
D) 5
E) 8
Question
The major product obtained from <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px> is:

A) <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which reagent can be used to accomplish the following transformation? <strong>Which reagent can be used to accomplish the following transformation?  </strong> A) pyridinium chlorochromate B) Tollens' reagent C) NaBH<sub>4</sub> D) H<sub>2</sub>, Ni E) NaH <div style=padding-top: 35px>

A) pyridinium chlorochromate
B) Tollens' reagent
C) NaBH4
D) H2, Ni
E) NaH
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Deck 9: Aldehydes and Ketones
1
Which of the hydrogens in the following molecule are most acidic? The hydrogens on carbon <strong>Which of the hydrogens in the following molecule are most acidic? The hydrogens on carbon  </strong> A) 1 B) 2 C) 3 D) 4 E) 5

A) 1
B) 2
C) 3
D) 4
E) 5
2
2
What is the structure of cyclohexanecarbaldehyde?

A) <strong>What is the structure of cyclohexanecarbaldehyde?</strong> A)   B)   C)   D)   E)
B) <strong>What is the structure of cyclohexanecarbaldehyde?</strong> A)   B)   C)   D)   E)
C) <strong>What is the structure of cyclohexanecarbaldehyde?</strong> A)   B)   C)   D)   E)
D) <strong>What is the structure of cyclohexanecarbaldehyde?</strong> A)   B)   C)   D)   E)
E) <strong>What is the structure of cyclohexanecarbaldehyde?</strong> A)   B)   C)   D)   E)
3
The enol tautomer of 3-pentanone is:

A) <strong>The enol tautomer of 3-pentanone is:</strong> A)   B)   C)   D)   E)
B) <strong>The enol tautomer of 3-pentanone is:</strong> A)   B)   C)   D)   E)
C) <strong>The enol tautomer of 3-pentanone is:</strong> A)   B)   C)   D)   E)
D) <strong>The enol tautomer of 3-pentanone is:</strong> A)   B)   C)   D)   E)
E) <strong>The enol tautomer of 3-pentanone is:</strong> A)   B)   C)   D)   E)
4
What class of compound most closely resembles an acetal in its reactivity with CH3MgBr?

A) ethers
B) aldehydes
C) ketones
D) alcohols
E) thiols
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5
Which of the following compounds is a cyanohydrin?

A) <strong>Which of the following compounds is a cyanohydrin?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the following compounds is a cyanohydrin?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the following compounds is a cyanohydrin?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the following compounds is a cyanohydrin?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the following compounds is a cyanohydrin?</strong> A)   B)   C)   D)   E)
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6
Which of the following compounds is a hemiacetal?

A) <strong>Which of the following compounds is a hemiacetal?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the following compounds is a hemiacetal?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the following compounds is a hemiacetal?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the following compounds is a hemiacetal?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the following compounds is a hemiacetal?</strong> A)   B)   C)   D)   E)
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7
The number of a-hydrogens in <strong>The number of a-hydrogens in   is:</strong> A) 1 B) 3 C) 4 D) 8 E) 14 is:

A) 1
B) 3
C) 4
D) 8
E) 14
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8
Which of the following molecules is a hemiacetal?

A) <strong>Which of the following molecules is a hemiacetal?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the following molecules is a hemiacetal?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the following molecules is a hemiacetal?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the following molecules is a hemiacetal?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the following molecules is a hemiacetal?</strong> A)   B)   C)   D)   E)
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9
Which of the following aldehydes can exist in equilibrium with a cyclic hemiacetal?

A) 4-pentenal
B) 3-hydroxypropanal
C) 2-hydroxybutanal
D) 3-hydroxybutanal
E) 4-hydroxybutanal
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10
The equilibrium that exists between the keto and enol forms of aldehydes and ketones is known as:

A) stereoisomerism
B) configurational isomerism
C) geometric isomerism
D) tautomerism
E) positional isomerism
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11
The name of the following is:
<strong>The name of the following is:   </strong> A) 2-hydroxy-4-pentanone. B) 2-oxo-4-pentanol. C) 4-oxo-2-pentanol. D) 1-acetyl-2-propanol. E) 4-hydroxy-2-pentanone.

A) 2-hydroxy-4-pentanone.
B) 2-oxo-4-pentanol.
C) 4-oxo-2-pentanol.
D) 1-acetyl-2-propanol.
E) 4-hydroxy-2-pentanone.
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12
The expected order of boiling points of the following is: <strong>The expected order of boiling points of the following is:  </strong> A) 3>2>1 B) 2>1>3 C) 2>3>1 D) 1>2>3 E) 1>3>2

A) 3>2>1
B) 2>1>3
C) 2>3>1
D) 1>2>3
E) 1>3>2
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13
The predominant product from the reaction below is: <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)

A) <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)
B) <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)
C) <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)
D) <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)
E) <strong>The predominant product from the reaction below is:  </strong> A)   B)   C)   D)   E)
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14
The IUPAC name for ethyl methyl ketone is

A) 2-butanone
B) 2-pentanone
C) 3-pentanone
D) propanone
E) acetophenone
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15
Which of the following molecules has the highest boiling point?

A) o-xylene
B) m-xylene
C) p-xylene
D) benzaldehyde
E) benzyl alcohol
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16
The IUPAC name for the following molecule is: <strong>The IUPAC name for the following molecule is:  </strong> A) 3-ethyl-1-phenyl-3-pentenone B) 3-ethyl-5-phenyl-2-penten-4-one C) allyl benzyl ketone D) (E)-3-ethyl-1-phenyl-3-penten-2-one E) (Z)-3-ethyl-1-phenyl-3-penten-2-one

A) 3-ethyl-1-phenyl-3-pentenone
B) 3-ethyl-5-phenyl-2-penten-4-one
C) allyl benzyl ketone
D) (E)-3-ethyl-1-phenyl-3-penten-2-one
E) (Z)-3-ethyl-1-phenyl-3-penten-2-one
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17
What is the class of compound produced from the reaction of a ketone with hydrazine?

A) oxime
B) amide
C) hydrazone
D) semicarbazone
E) imide
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18
The common name for the following molecule is: <strong>The common name for the following molecule is:  </strong> A) acetaldehyde B) dimethyl aldehyde C) ethyl ketone D) formaldehyde E) methylmethanal

A) acetaldehyde
B) dimethyl aldehyde
C) ethyl ketone
D) formaldehyde
E) methylmethanal
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19
Which of the following is a hydrazone?

A) <strong>Which of the following is a hydrazone?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the following is a hydrazone?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the following is a hydrazone?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the following is a hydrazone?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the following is a hydrazone?</strong> A)   B)   C)   D)   E)
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20
In a carbonyl group

A) the oxygen acts as a Lewis acid.
B) the C=O bond length is shortened due to resonance.
C) the carbon is sp3 hybridized.
D) the carbon is nucleophilic and the oxygen is electrophilic.
E) the carbon is electrophilic and the oxygen is nucleophilic.
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21
What type of compound is produced from the following reaction? <strong>What type of compound is produced from the following reaction?  </strong> A) an amide B) an alcohol C) an acid D) an aldehyde E) a ketone

A) an amide
B) an alcohol
C) an acid
D) an aldehyde
E) a ketone
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22
Which of the following nucleophiles add reversibly to a carbonyl group? <strong>Which of the following nucleophiles add reversibly to a carbonyl group?  </strong> A) I, II and IV B) II C) I and II D) III and IV E) I, II, III and IV

A) I, II and IV
B) II
C) I and II
D) III and IV
E) I, II, III and IV
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23
Which hydrogens in the following compound will be exchanged most rapidly for deuterium upon reaction with D2O and NaOD? <strong>Which hydrogens in the following compound will be exchanged most rapidly for deuterium upon reaction with D<sub>2</sub>O and NaOD?  </strong> A) H<sub>1</sub> B) H<sub>2</sub> C) H<sub>3</sub> D) H<sub>4</sub> E) H<sub>5</sub>

A) H1
B) H2
C) H3
D) H4
E) H5
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24
In the mechanism for acid catalyzed hemiacetal formation, the first step is:

A) protonation of the carbonyl oxygen
B) nucleophilic attack at the carbonyl carbon
C) protonation of the oxygen of the alcohol
D) nucleophilic attack at the carbon of the alcohol
E) elimination of a water molecule
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25
Which of the following compounds will not act as a nucleophile in an Aldol reaction?

A) <strong>Which of the following compounds will not act as a nucleophile in an Aldol reaction?</strong> A)   B)   C)   D) HCHO E) C and D
B) <strong>Which of the following compounds will not act as a nucleophile in an Aldol reaction?</strong> A)   B)   C)   D) HCHO E) C and D
C) <strong>Which of the following compounds will not act as a nucleophile in an Aldol reaction?</strong> A)   B)   C)   D) HCHO E) C and D
D) HCHO
E) C and D
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26
What statement is false relative to the nucleophilic additions?

A) When a weak nucleophile is present, the reaction can be catalyzed by acid.
B) The nucleophile attacks the trigonal carbon of the carbonyl group.
C) Ketones are more reactive than aldehydes.
D) Nucleophiles that add irreversibly are poor leaving groups.
E) Nucleophiles can be classified as those that add reversibly to carbonyl compounds and those that add irreversibly.
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27
Which statement about the mechanism of imine formation from a primary amine and an aldehyde or ketone is false?

A) The first steps involve addition of the amine to the carbonyl carbon to form a tetrahedral intermediate.
B) The last steps involve elimination of water to form a carbon-nitrogen p-bond.
C) All steps are reversible.
D) The reaction involves SN2 displacement of the carbonyl oxygen by the amine nitrogen.
E) The reaction does not require a strong acid catalyst.
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28
Which of the following reactions will produce a cyanohydrin?

A) <strong>Which of the following reactions will produce a cyanohydrin?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the following reactions will produce a cyanohydrin?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the following reactions will produce a cyanohydrin?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the following reactions will produce a cyanohydrin?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the following reactions will produce a cyanohydrin?</strong> A)   B)   C)   D)   E)
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29
The products from <strong>The products from   are:</strong> A)   B)   C)   D)   E) no reaction are:

A) <strong>The products from   are:</strong> A)   B)   C)   D)   E) no reaction
B) <strong>The products from   are:</strong> A)   B)   C)   D)   E) no reaction
C) <strong>The products from   are:</strong> A)   B)   C)   D)   E) no reaction
D) <strong>The products from   are:</strong> A)   B)   C)   D)   E) no reaction
E) no reaction
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30
Which of the following compounds will give a positive silver mirror test (Tollens' test)?

A) <strong>Which of the following compounds will give a positive silver mirror test (Tollens' test)?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the following compounds will give a positive silver mirror test (Tollens' test)?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the following compounds will give a positive silver mirror test (Tollens' test)?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the following compounds will give a positive silver mirror test (Tollens' test)?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the following compounds will give a positive silver mirror test (Tollens' test)?</strong> A)   B)   C)   D)   E)
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31
What is the structure of the aldol produced from reacting propanone with NaOH?

A) <strong>What is the structure of the aldol produced from reacting propanone with NaOH?</strong> A)   B)   C)   D)   E)
B) <strong>What is the structure of the aldol produced from reacting propanone with NaOH?</strong> A)   B)   C)   D)   E)
C) <strong>What is the structure of the aldol produced from reacting propanone with NaOH?</strong> A)   B)   C)   D)   E)
D) <strong>What is the structure of the aldol produced from reacting propanone with NaOH?</strong> A)   B)   C)   D)   E)
E) <strong>What is the structure of the aldol produced from reacting propanone with NaOH?</strong> A)   B)   C)   D)   E)
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32
The second step in the base catalyzed aldol condensation is:

A) formation of the enolate ion
B) addition of an enolate to a carbonyl group
C) protonation of the alkoxide ion
D) protonation of the carbonyl oxygen
E) loss of a proton from the α\alpha carbon
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33
Which reagent will accomplish the following transformation? <strong>Which reagent will accomplish the following transformation?  </strong> A) NaOH B) CrO<sub>3</sub>, H<sub>2</sub>SO<sub>4</sub> C) CH<sub>3</sub>MgBr D) NaBH<sub>4</sub> E) H<sub>2</sub>, Pd

A) NaOH
B) CrO3, H2SO4
C) CH3MgBr
D) NaBH4
E) H2, Pd
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34
What reaction will produce the following product? <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)

A) <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)
B) <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)
C) <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)
D) <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)
E) <strong>What reaction will produce the following product?  </strong> A)   B)   C)   D)   E)
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35
What Grignard reagent and carbonyl compound react to give benzyl alcohol after treatment with aqueous acid?

A) phenyl magnesium bromide and formaldehyde
B) phenyl magnesium bromide and oxirane
C) benzaldehyde and methyl magnesium bromide
D) benzaldehyde and ethyl magnesium chloride
E) acetophenone and methyl magnesium chloride
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36
Which reagents would you use to accomplish the following conversion? <strong>Which reagents would you use to accomplish the following conversion?  </strong> A) NaBH<sub>4</sub>, H<sub>2</sub>O B) LiAlH<sub>4</sub>, ether; then H<sub>3</sub>O<sup>+</sup> C) H<sub>2</sub>, Pt D) all of these E) none of these

A) NaBH4, H2O
B) LiAlH4, ether; then H3O+
C) H2, Pt
D) all of these
E) none of these
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37
An oxime can be produced by the reaction of an aldehyde and:

A) hydroxylamine
B) hydrazine
C) methylamine
D) phenylhydrazine
E) semicarbazide
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38
The product from <strong>The product from   is:</strong> A)   B)   C)   D)   E)   is:

A) <strong>The product from   is:</strong> A)   B)   C)   D)   E)
B) <strong>The product from   is:</strong> A)   B)   C)   D)   E)
C) <strong>The product from   is:</strong> A)   B)   C)   D)   E)
D) <strong>The product from   is:</strong> A)   B)   C)   D)   E)
E) <strong>The product from   is:</strong> A)   B)   C)   D)   E)
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39
The reaction of a Grignard reagent with acetone followed by acid hydrolysis will produce what type of product?

A) a primary alcohol
B) a secondary alcohol
C) a tertiary alcohol
D) a carboxylic acid
E) a ketone
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40
What reactants give the following molecule upon acid hydrolysis? <strong>What reactants give the following molecule upon acid hydrolysis?  </strong> A) cyclohexyl magnesium bromide and acetaldehyde B) cyclohexanol and   C) cyclohexanone and   D) cyclohexanecarbaldehyde and   E) cyclohexanone and ethenyl magnesium bromide

A) cyclohexyl magnesium bromide and acetaldehyde
B) cyclohexanol and <strong>What reactants give the following molecule upon acid hydrolysis?  </strong> A) cyclohexyl magnesium bromide and acetaldehyde B) cyclohexanol and   C) cyclohexanone and   D) cyclohexanecarbaldehyde and   E) cyclohexanone and ethenyl magnesium bromide
C) cyclohexanone and <strong>What reactants give the following molecule upon acid hydrolysis?  </strong> A) cyclohexyl magnesium bromide and acetaldehyde B) cyclohexanol and   C) cyclohexanone and   D) cyclohexanecarbaldehyde and   E) cyclohexanone and ethenyl magnesium bromide
D) cyclohexanecarbaldehyde and <strong>What reactants give the following molecule upon acid hydrolysis?  </strong> A) cyclohexyl magnesium bromide and acetaldehyde B) cyclohexanol and   C) cyclohexanone and   D) cyclohexanecarbaldehyde and   E) cyclohexanone and ethenyl magnesium bromide
E) cyclohexanone and ethenyl magnesium bromide
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41
The aldol obtained by treating <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)   with base is:

A) <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)
B) <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)
C) <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)
D) <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)
E) <strong>The aldol obtained by treating   with base is:</strong> A)   B)   C)   D)   E)
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42
The organic product of the reaction <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)   is:

A) <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)
B) <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)
C) <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)
D) <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)
E) <strong>The organic product of the reaction   is:</strong> A)   B)   C)   D)   E)
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43
How many hydrogens in the following compound will be exchanged for deuterium upon reaction with D2O and an acid catalyst? <strong>How many hydrogens in the following compound will be exchanged for deuterium upon reaction with D<sub>2</sub>O and an acid catalyst?  </strong> A) 0 B) 2 C) 4 D) 5 E) 8

A) 0
B) 2
C) 4
D) 5
E) 8
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44
The major product obtained from <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)   is:

A) <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)
B) <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)
C) <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)
D) <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)
E) <strong>The major product obtained from   is:</strong> A)   B)   C)   D)   E)
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45
Which reagent can be used to accomplish the following transformation? <strong>Which reagent can be used to accomplish the following transformation?  </strong> A) pyridinium chlorochromate B) Tollens' reagent C) NaBH<sub>4</sub> D) H<sub>2</sub>, Ni E) NaH

A) pyridinium chlorochromate
B) Tollens' reagent
C) NaBH4
D) H2, Ni
E) NaH
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