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University of New England CHEM 1020 Chapter 9 -- Aldehydes and Ketones MULTIPLE CHOICE 1)The common name for the following molecule is: acetaldehyde dimethyl aldehyde ethyl ketone formaldehyde methylmethanal What is the structure of cyclohexanecarbaldehyde? D) E) C) The IUPAC name for ethyl methyl ketone is 2-butanone 2-pentanone 3-pentanone propanone acetophenone The IUPAC name for the following molecule is: 3-ethyl-1-phenyl-3-pentenone 3-ethyl-5-phenyl-2-penten-4-one allyl benzyl ketone (E)-3-ethyl-1-phenyl-3-penten-2-one (Z)-3-ethyl-1-phenyl-3-penten-2-one What is the class of compound produced from the reaction of a ketone with hydrazine? oxime amide hydrazone semicarbazone imide Which of the following molecules is a hemiacetal? D) E) C) Which of the following compounds is a hemiacetal? D) E) C) Which of the following compounds is a cyanohydrin? D) E) C) Which of the following is a hydrazone? A) B) C) D) E) The name of the following is: 2-hydroxy-4-pentanone
University of New England
CHEM 1020
Chapter 9 -- Aldehydes and Ketones
MULTIPLE CHOICE
1)The common name for the following molecule is:
![]() |
-
- acetaldehyde
- dimethyl aldehyde
- ethyl ketone
- formaldehyde
- methylmethanal
- What is the structure of cyclohexanecarbaldehyde?
-


D) - E)
-

![]() |
C)
- The IUPAC name for ethyl methyl ketone is
- 2-butanone
- 2-pentanone
- 3-pentanone
- propanone
- acetophenone
- The IUPAC name for the following molecule is:
![]() |
-
- 3-ethyl-1-phenyl-3-pentenone
- 3-ethyl-5-phenyl-2-penten-4-one
- allyl benzyl ketone
- (E)-3-ethyl-1-phenyl-3-penten-2-one
- (Z)-3-ethyl-1-phenyl-3-penten-2-one
- What is the class of compound produced from the reaction of a ketone with hydrazine?
- oxime
- amide
- hydrazone
- semicarbazone
- imide
- Which of the following molecules is a hemiacetal?
D)

-

E)
C)

- Which of the following compounds is a hemiacetal?
- D)

-
-

E)
-
C)

- Which of the following compounds is a cyanohydrin?
D)
![]() |
-
- E)


C)
- Which of the following is a hydrazone?
A)
B)

C)
D)
E)
-

The name of the following is:
-
- 2-hydroxy-4-pentanone.
- 2-oxo-4-pentanol.
- 4-oxo-2-pentanol.
-
- 1-acetyl-2-propanol.
- 4-hydroxy-2-pentanone.
- Which of the following molecules has the highest boiling point?
- o-xylene
- m-xylene
- p-xylene
- benzaldehyde
- benzyl alcohol
- Which of the following aldehydes can exist in equilibrium with a cyclic hemiacetal?
- 4-pentenal
- 3-hydroxypropanal
- 2-hydroxybutanal
- 3-hydroxybutanal
- 4-hydroxybutanal
- What class of compound most closely resembles an acetal in its reactivity with CH3MgBr?
- ethers
- aldehydes
- ketones
- alcohols
- thiols
- In a carbonyl group
- the oxygen acts as a Lewis acid.
- the C=O bond length is shortened due to resonance.
- the carbon is sp3 hybridized.
- the carbon is nucleophilic and the oxygen is electrophilic.
- the carbon is electrophilic and the oxygen is nucleophilic.
- The expected order of boiling points of the following is:
![]() |
A) 3>2>1
B) 2>1>3
C) 2>3>1
D) 1>2>3
E) 1>3>2
- Which of the hydrogens in the following molecule are most acidic? The hydrogens on carbon
![]() |
-
- 1
- 2
- 3
- 4
- 5
- The equilibrium that exists between the keto and enol forms of aldehydes and ketones is known as:
- stereoisomerism
- configurational isomerism
- geometric isomerism
- tautomerism
- positional isomerism
- The number of a-hydrogens in is:
- 1
- 3
- 4
- 8
- 14
- The predominant product from the reaction below is:
![]() |
-
-

D)
-

-
-

E)
-
![]() |
C)
- The enol tautomer of 3-pentanone is:

D)
-
E)

C)
- Which hydrogens in the following compound will be exchanged most rapidly for deuterium upon reaction with D2O and NaOD?
![]() |
-
- H1
- H2
- H3
- H4
- H5
- In the mechanism for acid catalyzed hemiacetal formation, the first step is:
- protonation of the carbonyl oxygen
- nucleophilic attack at the carbonyl carbon
- protonation of the oxygen of the alcohol
- nucleophilic attack at the carbon of the alcohol
- elimination of a water molecule
- The second step in the base catalyzed aldol condensation is:
- formation of the enolate ion
- addition of an enolate to a carbonyl group
- protonation of the alkoxide ion
- protonation of the carbonyl oxygen
- loss of a proton from the ? carbon
- What statement is false relative to the nucleophilic additions?
- When a weak nucleophile is present, the reaction can be catalyzed by acid.
- The nucleophile attacks the trigonal carbon of the carbonyl group.
- Ketones are more reactive than aldehydes.
- Nucleophiles that add irreversibly are poor leaving groups.
Nucleophiles can be classified as those that add reversibly to carbonyl compounds and those that add irreversibly.
- Which statement about the mechanism of imine formation from a primary amine and an aldehyde or ketone is false?
- The first steps involve addition of the amine to the carbonyl carbon to form a tetrahedral intermediate.
- The last steps involve elimination of water to form a carbon-nitrogen p-bond.
- All steps are reversible.
- The reaction involves SN2 displacement of the carbonyl oxygen by the amine nitrogen.
- The reaction does not require a strong acid catalyst.
- Which of the following nucleophiles add reversibly to a carbonyl group?
![]() |
-
- I, II and IV
- II
- I and II
- III and IV
-
- I, II, III and IV
- What type of compound is produced from the following reaction?
![]() |
-
- an amide
- an alcohol
- an acid
- an aldehyde
- a ketone
- An oxime can be produced by the reaction of an aldehyde and:
- hydroxylamine
- hydrazine
- methylamine
- phenylhydrazine
- semicarbazide
- Which of the following compounds will not act as a nucleophile in an Aldol reaction?
A)
B)
C)
- HCHO
- C and D
- What reaction will produce the following product?
![]() |
A)

B)
C)
D)
E)
- The reaction of a Grignard reagent with acetone followed by acid hydrolysis will produce what type of product?
- a primary alcohol
- a secondary alcohol
- a tertiary alcohol
- a carboxylic acid
- a ketone
- Which reagents would you use to accomplish the following conversion?
![]() |
-
- NaBH4, H2O
- LiAlH4, ether; then H3O+
- H2, Pt
- all of these
- none of these
- Which of the following reactions will produce a cyanohydrin?
A)
B)
C)
D)
E)
- What Grignard reagent and carbonyl compound react to give benzyl alcohol after treatment with aqueous acid?
- phenyl magnesium bromide and formaldehyde
- phenyl magnesium bromide and oxirane
- benzaldehyde and methyl magnesium bromide
- benzaldehyde and ethyl magnesium chloride
- acetophenone and methyl magnesium chloride
- Which reagent will accomplish the following transformation?
![]() |
-
- NaOH
- CrO3, H2SO4
- CH3MgBr
- NaBH4
- H2, Pd
- What is the structure of the aldol produced from reacting propanone with NaOH?
![]() |
A)
B)
C)
D)
E)
-

What reactants give the following molecule upon acid hydrolysis?
-
cyclohexyl magnesium bromide and acetaldehyde- cyclohexanol and
- cyclohexanone and
- cyclohexanecarbaldehyde and
- cyclohexanone and ethenyl magnesium bromide
- The products from are:
A)
B)
C)

![]() |
D)
E) no reaction
- can be prepared from:
A)
B)
C)

![]() |
D)
E)

- The product from is:
A)
B)
![]() |
C)
D)

E)
- Which of the following compounds will give a positive silver mirror test (Tollens' test)?
D)

-

E)
C)
- The aldol obtained by treating with base is:
A)
B)
C)
D)
E)
The major product obtained from is:
-
-


D) - E)
-

![]() |
C)
- A reaction sequence that will accomplish the transformation below is:
![]() |
-
- 1. CH3MgBr 2. H3O+
- 1. CH3Li 2. H3O+ 3. CrO3, H2SO4
- 1. LiAlH4 2. H3O+ 3. CH3MgBr
- 1. H2, Pd catalyst 2. CH3MgBr 3. H3O+
- 1. CrO3, H2SO4 2. CH3MgBr 3. H3O+
- The organic product of the reaction is:
-
- D)

-
E)

C)

- How many hydrogens in the following compound will be exchanged for deuterium upon reaction with D2O and an acid catalyst?
![]() |
-
- 0
- 2
- 4
- 5
- 8
- Which reagent can be used to accomplish the following transformation?
![]() |
-
- pyridinium chlorochromate
- Tollens' reagent
- NaBH4
- H2, Ni
- NaH
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