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CHEM 219 Module 6 (PDF) | (2026) Aldehydes & Ketones | Practice Exam

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Master the CHEM 219 Module 6 exam with 500 practice questions covering aldehydes and ketones, including structure, nomenclature, properties, polarity, reactivity, and fundamental organic reactions. Strengthen your understanding of carbonyl chemistry and prepare efficiently with focused practice and detailed explanations.CHEM 219 Module, CHEM 219 Exam, CHEM 219 Practice, CHEM 219 Questions, CHEM 219 Study, Module 6 Exam, CHEM Module 6, Aldehydes Exam, Ketones Exam, Aldehyde Chemistry, Ketone Chemistry, Carbonyl Chemistry, Organic Reactions, Organic Chemistry, CHEM 219 Prep, CHEM 219 Guide, Portage CHEM, Organic Exam Prep, Chemistry Practice, Chemistry Study Guide

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CHEM 219: Organic Chemistry - Module 6
Exam
Aldehydes & Ketones: Structure, Properties & Reactions
Portage Learning Mastery - 500 Verified Questions (2026 Edition)



Functional Group Identification
Q1: What is the primary structural difference between an aldehyde and a ketone?
A. Aldehydes have a carbonyl group, ketones do not.
B. Ketones are at the end of a carbon chain, aldehydes are in the middle.
C. Aldehydes have the carbonyl carbon bonded to at least one hydrogen; ketones have it bonded to two
carbons.
D. Aldehydes contain nitrogen, while ketones only contain oxygen.
Answer: C
Study Note: The carbonyl group (C=O) in an aldehyde is terminal (attached to at least one H), while in a ketone, it is internal
(attached to two other carbon atoms).


Nomenclature
Q2: What is the IUPAC name for a three-carbon ketone?
A. Propanal
B. Propanone
C. Propanoic acid
D. Isopropanol
Answer: B
Study Note: The three-carbon alkane is propane. For a ketone, the suffix '-e' is replaced with '-one'. Propanone is also commonly
known as acetone.


Oxidation Reactions
Q3: Which of the following will occur when an aldehyde is treated with an oxidizing
agent like Tollens' reagent?
A. It is reduced to a primary alcohol.
B. It is oxidized to a carboxylic acid.
C. It is converted into a ketone.
D. No reaction occurs.
Answer: B
Study Note: Aldehydes are easily oxidized to carboxylic acids. Tollens' reagent (silver mirror test) is a classic test for the presence
of an aldehyde.




CHEM 219 Module 6 - Page 1

,Reduction Reactions
Q4: Reducing a ketone with NaBH4 (Sodium Borohydride) results in the formation of a:
A. Primary alcohol
B. Secondary alcohol
C. Tertiary alcohol
D. Carboxylic acid
Answer: B
Study Note: Reduction of a ketone adds hydrogen across the C=O bond, resulting in a secondary alcohol. Reduction of an
aldehyde results in a primary alcohol.


Physical Properties
Q5: Aldehydes and ketones have lower boiling points than alcohols of similar mass
because:
A. They are non-polar.
B. They cannot form hydrogen bonds with each other.
C. They have higher molar masses.
D. They are gases at room temperature.
Answer: B
Study Note: Unlike alcohols, aldehydes and ketones do not have an H atom directly bonded to the oxygen, so they cannot form
intermolecular hydrogen bonds.


Functional Group Identification
Q6: What is the primary structural difference between an aldehyde and a ketone?
A. Aldehydes have a carbonyl group, ketones do not.
B. Ketones are at the end of a carbon chain, aldehydes are in the middle.
C. Aldehydes have the carbonyl carbon bonded to at least one hydrogen; ketones have it bonded to two
carbons.
D. Aldehydes contain nitrogen, while ketones only contain oxygen.
Answer: C
Study Note: The carbonyl group (C=O) in an aldehyde is terminal (attached to at least one H), while in a ketone, it is internal
(attached to two other carbon atoms).


Nomenclature
Q7: What is the IUPAC name for a three-carbon ketone?
A. Propanal
B. Propanone
C. Propanoic acid
D. Isopropanol
Answer: B
Study Note: The three-carbon alkane is propane. For a ketone, the suffix '-e' is replaced with '-one'. Propanone is also commonly
known as acetone.




CHEM 219 Module 6 - Page 2

,Oxidation Reactions
Q8: Which of the following will occur when an aldehyde is treated with an oxidizing
agent like Tollens' reagent?
A. It is reduced to a primary alcohol.
B. It is oxidized to a carboxylic acid.
C. It is converted into a ketone.
D. No reaction occurs.
Answer: B
Study Note: Aldehydes are easily oxidized to carboxylic acids. Tollens' reagent (silver mirror test) is a classic test for the presence
of an aldehyde.


Reduction Reactions
Q9: Reducing a ketone with NaBH4 (Sodium Borohydride) results in the formation of a:
A. Primary alcohol
B. Secondary alcohol
C. Tertiary alcohol
D. Carboxylic acid
Answer: B
Study Note: Reduction of a ketone adds hydrogen across the C=O bond, resulting in a secondary alcohol. Reduction of an
aldehyde results in a primary alcohol.


Physical Properties
Q10: Aldehydes and ketones have lower boiling points than alcohols of similar mass
because:
A. They are non-polar.
B. They cannot form hydrogen bonds with each other.
C. They have higher molar masses.
D. They are gases at room temperature.
Answer: B
Study Note: Unlike alcohols, aldehydes and ketones do not have an H atom directly bonded to the oxygen, so they cannot form
intermolecular hydrogen bonds.


Functional Group Identification
Q11: What is the primary structural difference between an aldehyde and a ketone?
A. Aldehydes have a carbonyl group, ketones do not.
B. Ketones are at the end of a carbon chain, aldehydes are in the middle.
C. Aldehydes have the carbonyl carbon bonded to at least one hydrogen; ketones have it bonded to two
carbons.
D. Aldehydes contain nitrogen, while ketones only contain oxygen.
Answer: C
Study Note: The carbonyl group (C=O) in an aldehyde is terminal (attached to at least one H), while in a ketone, it is internal
(attached to two other carbon atoms).




CHEM 219 Module 6 - Page 3

, Nomenclature
Q12: What is the IUPAC name for a three-carbon ketone?
A. Propanal
B. Propanone
C. Propanoic acid
D. Isopropanol
Answer: B
Study Note: The three-carbon alkane is propane. For a ketone, the suffix '-e' is replaced with '-one'. Propanone is also commonly
known as acetone.


Oxidation Reactions
Q13: Which of the following will occur when an aldehyde is treated with an oxidizing
agent like Tollens' reagent?
A. It is reduced to a primary alcohol.
B. It is oxidized to a carboxylic acid.
C. It is converted into a ketone.
D. No reaction occurs.
Answer: B
Study Note: Aldehydes are easily oxidized to carboxylic acids. Tollens' reagent (silver mirror test) is a classic test for the presence
of an aldehyde.


Reduction Reactions
Q14: Reducing a ketone with NaBH4 (Sodium Borohydride) results in the formation of a:
A. Primary alcohol
B. Secondary alcohol
C. Tertiary alcohol
D. Carboxylic acid
Answer: B
Study Note: Reduction of a ketone adds hydrogen across the C=O bond, resulting in a secondary alcohol. Reduction of an
aldehyde results in a primary alcohol.


Physical Properties
Q15: Aldehydes and ketones have lower boiling points than alcohols of similar mass
because:
A. They are non-polar.
B. They cannot form hydrogen bonds with each other.
C. They have higher molar masses.
D. They are gases at room temperature.
Answer: B
Study Note: Unlike alcohols, aldehydes and ketones do not have an H atom directly bonded to the oxygen, so they cannot form
intermolecular hydrogen bonds.




CHEM 219 Module 6 - Page 4

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