Deck 16: Aldehydes and Ketones

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Question
What is the condensed formula of the compound shown below? <strong>What is the condensed formula of the compound shown below?  </strong> A)CH<sub>3</sub>CO(CH<sub>2</sub>)<sub>3</sub>CH(CH<sub>3</sub>)<sub>2</sub> B)CH<sub>3</sub>OC(CH<sub>2</sub>)<sub>3</sub>CHCH<sub>3</sub>CH<sub>3</sub> C)CH<sub>3</sub>CO(CH<sub>2</sub>)<sub>3</sub>CHCH<sub>3</sub>CH<sub>3</sub> D)CH<sub>3</sub>OCCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH(CH<sub>3</sub>)<sub>2</sub> <div style=padding-top: 35px>

A)CH3CO(CH2)3CH(CH3)2
B)CH3OC(CH2)3CHCH3CH3
C)CH3CO(CH2)3CHCH3CH3
D)CH3OCCH2CH2CH2CH2CH(CH3)2
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Question
What product is formed when the compound below is oxidized with K2Cr2O7? <strong>What product is formed when the compound below is oxidized with K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>?  </strong> A)   B)   C)   D)No reaction occurs. <div style=padding-top: 35px>

A) <strong>What product is formed when the compound below is oxidized with K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>?  </strong> A)   B)   C)   D)No reaction occurs. <div style=padding-top: 35px>
B) <strong>What product is formed when the compound below is oxidized with K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>?  </strong> A)   B)   C)   D)No reaction occurs. <div style=padding-top: 35px>
C) <strong>What product is formed when the compound below is oxidized with K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>?  </strong> A)   B)   C)   D)No reaction occurs. <div style=padding-top: 35px>
D)No reaction occurs.
Question
The compound shown below belongs to what class of compounds? <strong>The compound shown below belongs to what class of compounds?  </strong> A)Alkane B)Aldehyde C)Ketone D)Acetal E)Carboxylic acid <div style=padding-top: 35px>

A)Alkane
B)Aldehyde
C)Ketone
D)Acetal
E)Carboxylic acid
Question
What is the structure of 1-chloro-3-ethyl-2-heptanone?

A) <strong>What is the structure of 1-chloro-3-ethyl-2-heptanone?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What is the structure of 1-chloro-3-ethyl-2-heptanone?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What is the structure of 1-chloro-3-ethyl-2-heptanone?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What is the structure of 1-chloro-3-ethyl-2-heptanone?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
The Tollens reagent is which of the following?

A)K2Cr2O7
B)H2SO4
C)Cl2
D)Ag2O in aqueous NH4OH
Question
The compound shown below belongs to what class of compounds? <strong>The compound shown below belongs to what class of compounds?  </strong> A)Alkane B)Aldehyde C)Ketone D)Acetal E)Carboxylic acid <div style=padding-top: 35px>

A)Alkane
B)Aldehyde
C)Ketone
D)Acetal
E)Carboxylic acid
Question
What is the common name of the compound shown below? <strong>What is the common name of the compound shown below?  </strong> A)Benzene aldehyde B)Benzaldehyde C)Acetaldehyde D)Phenone <div style=padding-top: 35px>

A)Benzene aldehyde
B)Benzaldehyde
C)Acetaldehyde
D)Phenone
Question
Which of the following represents the general condensed formula for an aldehyde?

A)RCOOH
B)RCHO
C)RCOR
D)RCOH
E)RCH2OH
Question
Which compound has the greatest solubility in water?

A)CH3(CH2)5CHO
B)CH3(CH2)4COCH2CH3
C)CH3CH2CHO
D)The compounds all are equally soluble in water.
Question
What is the IUPAC name of the compound shown below? <strong>What is the IUPAC name of the compound shown below?  </strong> A)5-chloro-3-methylhexanal B)2-chloro-4-methylhexanal C)5-chloro-3-methyl-6-hexanal D)2-chloro-4-methylhexanone E)3-chloro-5-methylhexanone <div style=padding-top: 35px>

A)5-chloro-3-methylhexanal
B)2-chloro-4-methylhexanal
C)5-chloro-3-methyl-6-hexanal
D)2-chloro-4-methylhexanone
E)3-chloro-5-methylhexanone
Question
Which compound is an example of a ketone?

A) <strong>Which compound is an example of a ketone?</strong> A)   B)   C)   D)   E)None of the structures are ketones. <div style=padding-top: 35px>
B) <strong>Which compound is an example of a ketone?</strong> A)   B)   C)   D)   E)None of the structures are ketones. <div style=padding-top: 35px>
C) <strong>Which compound is an example of a ketone?</strong> A)   B)   C)   D)   E)None of the structures are ketones. <div style=padding-top: 35px>
D) <strong>Which compound is an example of a ketone?</strong> A)   B)   C)   D)   E)None of the structures are ketones. <div style=padding-top: 35px>
E)None of the structures are ketones.
Question
Which compound is soluble in heptane,but not soluble in water?

A)(CH3)2CH(CH2)5CHO
B)CH3COCH3
C)CH3CH2CHO
D)All of the compounds are soluble in both heptane and water.
Question
Which compound has the highest boiling point?

A)CH3(CH2)5CH3
B)CH3(CH2)4CHO
C)CH3(CH2)4CH2OH
D)All of the compounds have the same boiling point.
Question
Which compound will give a positive result in a Tollens test?

A) <strong>Which compound will give a positive result in a Tollens test?</strong> A)   B)   C)   D)   E)More than one of the compounds will give a positive Tollens test result. <div style=padding-top: 35px>
B) <strong>Which compound will give a positive result in a Tollens test?</strong> A)   B)   C)   D)   E)More than one of the compounds will give a positive Tollens test result. <div style=padding-top: 35px>
C) <strong>Which compound will give a positive result in a Tollens test?</strong> A)   B)   C)   D)   E)More than one of the compounds will give a positive Tollens test result. <div style=padding-top: 35px>
D) <strong>Which compound will give a positive result in a Tollens test?</strong> A)   B)   C)   D)   E)More than one of the compounds will give a positive Tollens test result. <div style=padding-top: 35px>
E)More than one of the compounds will give a positive Tollens test result.
Question
Which compound(s)would give a positive Tollens test?

A)Alcohols
B)Aldehydes
C)Ketones
D)Carboxylic acids
E)Alcohols and aldehydes
Question
What is the IUPAC name of the compound shown below? <strong>What is the IUPAC name of the compound shown below?  </strong> A)Methyl hexyl ketone B)6,6-dimethyl-2-hexanone C)6-methyl-2-heptanone D)2-methyl-6-heptanone <div style=padding-top: 35px>

A)Methyl hexyl ketone
B)6,6-dimethyl-2-hexanone
C)6-methyl-2-heptanone
D)2-methyl-6-heptanone
Question
Which is the structure of 3-bromo-2-methylbutanal?

A) <strong>Which is the structure of 3-bromo-2-methylbutanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which is the structure of 3-bromo-2-methylbutanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which is the structure of 3-bromo-2-methylbutanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which is the structure of 3-bromo-2-methylbutanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What is the IUPAC name of the compound shown below? <strong>What is the IUPAC name of the compound shown below?  </strong> A)1-pentanone B)Cyclopentanone C)Phenone D)Cyclopentone <div style=padding-top: 35px>

A)1-pentanone
B)Cyclopentanone
C)Phenone
D)Cyclopentone
Question
What is the structure of 2-ethyl-4-methyloctanal?

A) <strong>What is the structure of 2-ethyl-4-methyloctanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What is the structure of 2-ethyl-4-methyloctanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What is the structure of 2-ethyl-4-methyloctanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What is the structure of 2-ethyl-4-methyloctanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Which compound could be oxidized to form the carboxylic acid below? <strong>Which compound could be oxidized to form the carboxylic acid below?  </strong> A)CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CHO B)   C)   D)   <div style=padding-top: 35px>

A)CH3(CH2)5CHO
B) <strong>Which compound could be oxidized to form the carboxylic acid below?  </strong> A)CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CHO B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which compound could be oxidized to form the carboxylic acid below?  </strong> A)CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CHO B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which compound could be oxidized to form the carboxylic acid below?  </strong> A)CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CHO B)   C)   D)   <div style=padding-top: 35px>
Question
What hemiacetal is formed in the reaction below? <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What is the acetal formed in the reaction below,if two equivalents of alcohol are used? <strong>What is the acetal formed in the reaction below,if two equivalents of alcohol are used?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What is the acetal formed in the reaction below,if two equivalents of alcohol are used?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What is the acetal formed in the reaction below,if two equivalents of alcohol are used?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What is the acetal formed in the reaction below,if two equivalents of alcohol are used?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What is the acetal formed in the reaction below,if two equivalents of alcohol are used?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What product is formed when the following molecule is treated with H2 and a Pd catalyst? <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Which reactant would be needed to form the alcohol product CH3CH2CH2OH by a reduction reaction?

A) <strong>Which reactant would be needed to form the alcohol product CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH by a reduction reaction?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which reactant would be needed to form the alcohol product CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH by a reduction reaction?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which reactant would be needed to form the alcohol product CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH by a reduction reaction?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which reactant would be needed to form the alcohol product CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH by a reduction reaction?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What hemiacetal is formed in the reaction below? <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Which compound is a hemiacetal?

A) <strong>Which compound is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which compound is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which compound is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which compound is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which compound is a hemiacetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What reaction does the coenzyme NADH,in the presence of an enzyme,facilitate?

A)The reduction of a carbonyl group to form a carboxylic acid
B)The reduction of a carbonyl group to form an alcohol
C)The reduction of a carboxylic acid to form a carbonyl group
D)The oxidation of a carbonyl group to form an alcohol
E)The oxidation of a carbonyl group to form a carboxylic acid
Question
Which compound is an acetal?

A) <strong>Which compound is an acetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which compound is an acetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which compound is an acetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which compound is an acetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which compound is an acetal?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What product is formed when the compound shown below is treated with Tollens reagent? <strong>What product is formed when the compound shown below is treated with Tollens reagent?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What product is formed when the compound shown below is treated with Tollens reagent?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What product is formed when the compound shown below is treated with Tollens reagent?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What product is formed when the compound shown below is treated with Tollens reagent?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What product is formed when the compound shown below is treated with Tollens reagent?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
The compound below is classified as what type of compound? <strong>The compound below is classified as what type of compound?  </strong> A)An acetal B)A hemiacetal C)An ether D)An acetal and an ether <div style=padding-top: 35px>

A)An acetal
B)A hemiacetal
C)An ether
D)An acetal and an ether
Question
The compound below is classified as what type of compound? <strong>The compound below is classified as what type of compound?  </strong> A)An acetal B)A hemiacetal C)An ether D)A cyclic acetal E)An acetal and an ether <div style=padding-top: 35px>

A)An acetal
B)A hemiacetal
C)An ether
D)A cyclic acetal
E)An acetal and an ether
Question
What is the product of the reduction of a ketone?

A)A primary alcohol
B)A secondary alcohol
C)A tertiary alcohol
D)A carboxylic acid
E)An ether
Question
Which reactant would be needed to form the alcohol product shown below by a reduction reaction? <strong>Which reactant would be needed to form the alcohol product shown below by a reduction reaction?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>Which reactant would be needed to form the alcohol product shown below by a reduction reaction?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which reactant would be needed to form the alcohol product shown below by a reduction reaction?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which reactant would be needed to form the alcohol product shown below by a reduction reaction?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which reactant would be needed to form the alcohol product shown below by a reduction reaction?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What product is formed when the following molecule is treated with H2 and a Pd catalyst? <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized? <strong>What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH3CH2OH)in the presences of H2SO4? <strong>What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)in the presences of H<sub>2</sub>SO<sub>4</sub>?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)in the presences of H<sub>2</sub>SO<sub>4</sub>?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)in the presences of H<sub>2</sub>SO<sub>4</sub>?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)in the presences of H<sub>2</sub>SO<sub>4</sub>?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)in the presences of H<sub>2</sub>SO<sub>4</sub>?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What is the product of the reduction of an aldehyde?

A)A primary alcohol
B)A secondary alcohol
C)A tertiary alcohol
D)A carboxylic acid
E)An ether
Question
What products are formed when the acetal below is hydrolyzed with water and sulfuric acid? <strong>What products are formed when the acetal below is hydrolyzed with water and sulfuric acid?  </strong> A)   B)   C)HOCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> + 2 CH<sub>3</sub>OH D)   <div style=padding-top: 35px>

A) <strong>What products are formed when the acetal below is hydrolyzed with water and sulfuric acid?  </strong> A)   B)   C)HOCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> + 2 CH<sub>3</sub>OH D)   <div style=padding-top: 35px>
B) <strong>What products are formed when the acetal below is hydrolyzed with water and sulfuric acid?  </strong> A)   B)   C)HOCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> + 2 CH<sub>3</sub>OH D)   <div style=padding-top: 35px>
C)HOCH2CH2CH2CH2CH3 + 2 CH3OH
D) <strong>What products are formed when the acetal below is hydrolyzed with water and sulfuric acid?  </strong> A)   B)   C)HOCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> + 2 CH<sub>3</sub>OH D)   <div style=padding-top: 35px>
Question
A hemiacetal contains which two groups bonded to the same carbon atom?

A)An OH (hydroxyl)group and an OR (alkoxy)group
B)Two OH (hydroxyl)groups
C)Two OR (alkoxy)groups
D)An OH (hydroxyl)group and a C=O (carbonyl)group
Question
Which reagent can be used to reduce a ketone?

A)K2Cr2O7
B)H2SO4
C)H2 with Pd metal
D)Ag2O in aqueous NH4OH
Question
The following ketones play an important role in the tanning industry and are found in many commercial sunscreens. Which ketone is expected to be the most soluble in water and therefore the most readily washed off when an individual goes swimming?

A) <strong>The following ketones play an important role in the tanning industry and are found in many commercial sunscreens. Which ketone is expected to be the most soluble in water and therefore the most readily washed off when an individual goes swimming?</strong> A)   B)   C)   D)All would be expected to have the same solubility. <div style=padding-top: 35px>
B) <strong>The following ketones play an important role in the tanning industry and are found in many commercial sunscreens. Which ketone is expected to be the most soluble in water and therefore the most readily washed off when an individual goes swimming?</strong> A)   B)   C)   D)All would be expected to have the same solubility. <div style=padding-top: 35px>
C) <strong>The following ketones play an important role in the tanning industry and are found in many commercial sunscreens. Which ketone is expected to be the most soluble in water and therefore the most readily washed off when an individual goes swimming?</strong> A)   B)   C)   D)All would be expected to have the same solubility. <div style=padding-top: 35px>
D)All would be expected to have the same solubility.
Question
What product results when cinnamaldehyde is reduced with excess H2 in the presence of a Pd catalyst? <strong>What product results when cinnamaldehyde is reduced with excess H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What product results when cinnamaldehyde is reduced with excess H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What product results when cinnamaldehyde is reduced with excess H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What product results when cinnamaldehyde is reduced with excess H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What product results when cinnamaldehyde is reduced with excess H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What is the IUPAC name of the compound below? <strong>What is the IUPAC name of the compound below?  </strong> A)4-chloro-3-pentyl-1-cyclohexone B)4-chloro-3-pentylcyclohexanone C)1-chloro-2-pentyl-4-cyclohexanone D)4-chloro-3-pentylphenone <div style=padding-top: 35px>

A)4-chloro-3-pentyl-1-cyclohexone
B)4-chloro-3-pentylcyclohexanone
C)1-chloro-2-pentyl-4-cyclohexanone
D)4-chloro-3-pentylphenone
Question
The compound butanone does not need a number to specify the location of the carbonyl group on the carbon chain. Which statement best explains why?

A)The C=O is assumed to be on C-1 of the carbon chain if it is not specified.
B)The C=O can only be on C-2 of the carbon chain in this compound.
C)The location of the C=O does not need to be specified for a cyclic ketone.
D)The C=O is on an end carbon of the carbon chain.
Question
The compound decanal contributes to the odor and flavor of an orange. Which of the statements concerning the structure of decanal is incorrect?

A)Decanal is an aldehyde.
B)Decanal contains a saturated chain of ten carbons.
C)Decanal contains a carbonyl group on the first carbon of the carbon chain.
D)Decanal is an aromatic compound.
Question
What hydrolysis products are formed when the acetal (CH3CH2CH2)2C(OCH2CH3)2 is treated with H2SO4 in H2O?

A)(CH3CH2CH2)2CHOCH2CH3 + CH3CH2OH
B)(CH3CH2CH2)2CO + 2 CH3CH2OH
C)(CH3CH2CH2)2CHOH + 2 CH3CH2OH
D)CH2(OCH2CH3)2 + 2 CH3CH2CH3
Question
Deoxyribose is a building block of DNA. Which statement concerning the functional groups present in deoxyribose,shown below,is incorrect? <strong>Deoxyribose is a building block of DNA. Which statement concerning the functional groups present in deoxyribose,shown below,is incorrect?  </strong> A)It contains an acetal. B)It contains an alcohol. C)It contains a hemiacetal. D)None of these choices are incorrect. <div style=padding-top: 35px>

A)It contains an acetal.
B)It contains an alcohol.
C)It contains a hemiacetal.
D)None of these choices are incorrect.
Question
What is the name of the compound below? <strong>What is the name of the compound below?  </strong> A)3-bromo-4-ethyl-2-methylbenzaldehyde B)3-bromo-4-ethoxy-2-methoxybenzaldehyde C)1-bromo-2-ethoxy-6-methoxy-3-benzaldehyde D)3-bromo-4-ethoxy-2-methoxyphenal <div style=padding-top: 35px>

A)3-bromo-4-ethyl-2-methylbenzaldehyde
B)3-bromo-4-ethoxy-2-methoxybenzaldehyde
C)1-bromo-2-ethoxy-6-methoxy-3-benzaldehyde
D)3-bromo-4-ethoxy-2-methoxyphenal
Question
What type of compound is shown below? <strong>What type of compound is shown below?  </strong> A)An epoxide B)A cyclic hemiacetal C)An aldehyde D)A cyclic acetal <div style=padding-top: 35px>

A)An epoxide
B)A cyclic hemiacetal
C)An aldehyde
D)A cyclic acetal
Question
What is the structure of 2-bromo-5-hydroxyheptanal?

A) <strong>What is the structure of 2-bromo-5-hydroxyheptanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What is the structure of 2-bromo-5-hydroxyheptanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What is the structure of 2-bromo-5-hydroxyheptanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What is the structure of 2-bromo-5-hydroxyheptanal?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Salicin is a naturally occurring pain reliever isolated from the bark of willow trees. Which statement concerning the functional groups present in salicin is incorrect? <strong>Salicin is a naturally occurring pain reliever isolated from the bark of willow trees. Which statement concerning the functional groups present in salicin is incorrect?  </strong> A)It contains an acetal. B)It contains an alcohol. C)It contains a hemiacetal. D)It contains a phenol. <div style=padding-top: 35px>

A)It contains an acetal.
B)It contains an alcohol.
C)It contains a hemiacetal.
D)It contains a phenol.
Question
Which of the following is the product of the reduction of acetone,shown below? <strong>Which of the following is the product of the reduction of acetone,shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>Which of the following is the product of the reduction of acetone,shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>Which of the following is the product of the reduction of acetone,shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>Which of the following is the product of the reduction of acetone,shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>Which of the following is the product of the reduction of acetone,shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What product results when cinnamaldehyde is oxidized? <strong>What product results when cinnamaldehyde is oxidized?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>What product results when cinnamaldehyde is oxidized?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What product results when cinnamaldehyde is oxidized?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What product results when cinnamaldehyde is oxidized?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What product results when cinnamaldehyde is oxidized?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
In the correct order,what are the three reactions that convert all-trans-retinal into 11-cis-retinal so that the process of vision can continue?

A)Reduction,Oxidation,Isomerization
B)Reduction,Isomerization,Oxidation
C)Oxidation,Isomerization,Reduction
D)Oxidation,Reduction,Isomerization
Question
What is the name of the compound below? <strong>What is the name of the compound below?  </strong> A)1-methoxy-3-methylbenzene B)4-methoxy-6-methylbenzaldehyde C)4-methoxy-2-methylacetophenone D)5-methoxy-3-methyltoluene <div style=padding-top: 35px>

A)1-methoxy-3-methylbenzene
B)4-methoxy-6-methylbenzaldehyde
C)4-methoxy-2-methylacetophenone
D)5-methoxy-3-methyltoluene
Question
What type of compound is shown below? <strong>What type of compound is shown below?  </strong> A)An epoxide B)A cyclic hemiacetal C)An aldehyde D)A cyclic acetal <div style=padding-top: 35px>

A)An epoxide
B)A cyclic hemiacetal
C)An aldehyde
D)A cyclic acetal
Question
What is the name of the compound below? <strong>What is the name of the compound below?  </strong> A)3-chlorobenzenal B)3-methanalchlorobenzene C)M-chlorobenzaldehyde D)P-chloroacetophenone <div style=padding-top: 35px>

A)3-chlorobenzenal
B)3-methanalchlorobenzene
C)M-chlorobenzaldehyde
D)P-chloroacetophenone
Question
What is the name of the compound below? <strong>What is the name of the compound below?  </strong> A)2-ethylbenzenone B)2-ethylacetophenone C)2-ethylacetobenzone D)2-ethylphenone <div style=padding-top: 35px>

A)2-ethylbenzenone
B)2-ethylacetophenone
C)2-ethylacetobenzone
D)2-ethylphenone
Question
What is the structure of 3-hydroxy-2-methylbenzaldehyde?

A) <strong>What is the structure of 3-hydroxy-2-methylbenzaldehyde?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>What is the structure of 3-hydroxy-2-methylbenzaldehyde?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>What is the structure of 3-hydroxy-2-methylbenzaldehyde?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>What is the structure of 3-hydroxy-2-methylbenzaldehyde?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction? <strong>The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
The reaction below illustrates oxidation of an aldehyde. The reaction below illustrates oxidation of an aldehyde.  <div style=padding-top: 35px>
Question
When light hits the retina,the 11-cis double bond of 11-cis-retinal is isomerized to its more stable trans isomer,and the all-trans-retinal is formed.
Question
The reaction below illustrates oxidation by Tollens reagent. The reaction below illustrates oxidation by Tollens reagent.  <div style=padding-top: 35px>
Question
Ketones are not oxidized since they contain no H atom bonded to the carbonyl carbon.
Question
Vanillin,acetone,and formaldehyde are aldehydes.
Question
The reaction below illustrates oxidation by Tollens' reagent. The reaction below illustrates oxidation by Tollens' reagent.  <div style=padding-top: 35px>
Question
When the hemiacetal below reacts with ethanol,what acetal is formed? <strong>When the hemiacetal below reacts with ethanol,what acetal is formed?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A) <strong>When the hemiacetal below reacts with ethanol,what acetal is formed?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B) <strong>When the hemiacetal below reacts with ethanol,what acetal is formed?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C) <strong>When the hemiacetal below reacts with ethanol,what acetal is formed?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D) <strong>When the hemiacetal below reacts with ethanol,what acetal is formed?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
The structure below contains both an acetal and hemiacetal. The structure below contains both an acetal and hemiacetal.  <div style=padding-top: 35px>
Question
Triamcinolone acetonide (structure shown),a synthetic corticosteroid drug,contains an acetal. Triamcinolone acetonide (structure shown),a synthetic corticosteroid drug,contains an acetal.  <div style=padding-top: 35px>
Question
4,4-Dimethyl-2-hexanone is a ketone of molecular formula C8H16O that has six carbons in its longest chain.
Question
The carbohydrate glucose exists predominantly as a cyclic hemiacetal.
Question
11-cis-retinal is a ketone in the rod cells of the eye that is critical for vision.
Question
Acetals are stable molecules,but they can be converted back to aldehydes and ketones by treatment with acid and water.
Question
Acetals are ethers.
Question
Cyclic hemiacetals are converted to acetals by reaction with an alcohol.
Question
Aldehydes and ketones undergo addition reactions with alcohols (ROH)to form hemiacetals and acetals.
Question
Aldehydes and ketones undergo addition reactions with alcohols (ROH)to form hemiacetals and acetals.
Question
As is in the laboratory,the reduction of carbonyl groups in biological systems is accomplished using H2 and Pd as a reducing agent.
Question
D-Glucose,shown below,will give a positive Tollens test. D-Glucose,shown below,will give a positive Tollens test.  <div style=padding-top: 35px>
Question
The compound below is an acetal. The compound below is an acetal.  <div style=padding-top: 35px>
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Deck 16: Aldehydes and Ketones
1
What is the condensed formula of the compound shown below? <strong>What is the condensed formula of the compound shown below?  </strong> A)CH<sub>3</sub>CO(CH<sub>2</sub>)<sub>3</sub>CH(CH<sub>3</sub>)<sub>2</sub> B)CH<sub>3</sub>OC(CH<sub>2</sub>)<sub>3</sub>CHCH<sub>3</sub>CH<sub>3</sub> C)CH<sub>3</sub>CO(CH<sub>2</sub>)<sub>3</sub>CHCH<sub>3</sub>CH<sub>3</sub> D)CH<sub>3</sub>OCCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH(CH<sub>3</sub>)<sub>2</sub>

A)CH3CO(CH2)3CH(CH3)2
B)CH3OC(CH2)3CHCH3CH3
C)CH3CO(CH2)3CHCH3CH3
D)CH3OCCH2CH2CH2CH2CH(CH3)2
CH3CO(CH2)3CH(CH3)2
2
What product is formed when the compound below is oxidized with K2Cr2O7? <strong>What product is formed when the compound below is oxidized with K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>?  </strong> A)   B)   C)   D)No reaction occurs.

A) <strong>What product is formed when the compound below is oxidized with K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>?  </strong> A)   B)   C)   D)No reaction occurs.
B) <strong>What product is formed when the compound below is oxidized with K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>?  </strong> A)   B)   C)   D)No reaction occurs.
C) <strong>What product is formed when the compound below is oxidized with K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>?  </strong> A)   B)   C)   D)No reaction occurs.
D)No reaction occurs.
3
The compound shown below belongs to what class of compounds? <strong>The compound shown below belongs to what class of compounds?  </strong> A)Alkane B)Aldehyde C)Ketone D)Acetal E)Carboxylic acid

A)Alkane
B)Aldehyde
C)Ketone
D)Acetal
E)Carboxylic acid
Aldehyde
4
What is the structure of 1-chloro-3-ethyl-2-heptanone?

A) <strong>What is the structure of 1-chloro-3-ethyl-2-heptanone?</strong> A)   B)   C)   D)
B) <strong>What is the structure of 1-chloro-3-ethyl-2-heptanone?</strong> A)   B)   C)   D)
C) <strong>What is the structure of 1-chloro-3-ethyl-2-heptanone?</strong> A)   B)   C)   D)
D) <strong>What is the structure of 1-chloro-3-ethyl-2-heptanone?</strong> A)   B)   C)   D)
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5
The Tollens reagent is which of the following?

A)K2Cr2O7
B)H2SO4
C)Cl2
D)Ag2O in aqueous NH4OH
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6
The compound shown below belongs to what class of compounds? <strong>The compound shown below belongs to what class of compounds?  </strong> A)Alkane B)Aldehyde C)Ketone D)Acetal E)Carboxylic acid

A)Alkane
B)Aldehyde
C)Ketone
D)Acetal
E)Carboxylic acid
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7
What is the common name of the compound shown below? <strong>What is the common name of the compound shown below?  </strong> A)Benzene aldehyde B)Benzaldehyde C)Acetaldehyde D)Phenone

A)Benzene aldehyde
B)Benzaldehyde
C)Acetaldehyde
D)Phenone
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8
Which of the following represents the general condensed formula for an aldehyde?

A)RCOOH
B)RCHO
C)RCOR
D)RCOH
E)RCH2OH
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9
Which compound has the greatest solubility in water?

A)CH3(CH2)5CHO
B)CH3(CH2)4COCH2CH3
C)CH3CH2CHO
D)The compounds all are equally soluble in water.
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10
What is the IUPAC name of the compound shown below? <strong>What is the IUPAC name of the compound shown below?  </strong> A)5-chloro-3-methylhexanal B)2-chloro-4-methylhexanal C)5-chloro-3-methyl-6-hexanal D)2-chloro-4-methylhexanone E)3-chloro-5-methylhexanone

A)5-chloro-3-methylhexanal
B)2-chloro-4-methylhexanal
C)5-chloro-3-methyl-6-hexanal
D)2-chloro-4-methylhexanone
E)3-chloro-5-methylhexanone
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11
Which compound is an example of a ketone?

A) <strong>Which compound is an example of a ketone?</strong> A)   B)   C)   D)   E)None of the structures are ketones.
B) <strong>Which compound is an example of a ketone?</strong> A)   B)   C)   D)   E)None of the structures are ketones.
C) <strong>Which compound is an example of a ketone?</strong> A)   B)   C)   D)   E)None of the structures are ketones.
D) <strong>Which compound is an example of a ketone?</strong> A)   B)   C)   D)   E)None of the structures are ketones.
E)None of the structures are ketones.
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12
Which compound is soluble in heptane,but not soluble in water?

A)(CH3)2CH(CH2)5CHO
B)CH3COCH3
C)CH3CH2CHO
D)All of the compounds are soluble in both heptane and water.
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13
Which compound has the highest boiling point?

A)CH3(CH2)5CH3
B)CH3(CH2)4CHO
C)CH3(CH2)4CH2OH
D)All of the compounds have the same boiling point.
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14
Which compound will give a positive result in a Tollens test?

A) <strong>Which compound will give a positive result in a Tollens test?</strong> A)   B)   C)   D)   E)More than one of the compounds will give a positive Tollens test result.
B) <strong>Which compound will give a positive result in a Tollens test?</strong> A)   B)   C)   D)   E)More than one of the compounds will give a positive Tollens test result.
C) <strong>Which compound will give a positive result in a Tollens test?</strong> A)   B)   C)   D)   E)More than one of the compounds will give a positive Tollens test result.
D) <strong>Which compound will give a positive result in a Tollens test?</strong> A)   B)   C)   D)   E)More than one of the compounds will give a positive Tollens test result.
E)More than one of the compounds will give a positive Tollens test result.
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15
Which compound(s)would give a positive Tollens test?

A)Alcohols
B)Aldehydes
C)Ketones
D)Carboxylic acids
E)Alcohols and aldehydes
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16
What is the IUPAC name of the compound shown below? <strong>What is the IUPAC name of the compound shown below?  </strong> A)Methyl hexyl ketone B)6,6-dimethyl-2-hexanone C)6-methyl-2-heptanone D)2-methyl-6-heptanone

A)Methyl hexyl ketone
B)6,6-dimethyl-2-hexanone
C)6-methyl-2-heptanone
D)2-methyl-6-heptanone
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17
Which is the structure of 3-bromo-2-methylbutanal?

A) <strong>Which is the structure of 3-bromo-2-methylbutanal?</strong> A)   B)   C)   D)
B) <strong>Which is the structure of 3-bromo-2-methylbutanal?</strong> A)   B)   C)   D)
C) <strong>Which is the structure of 3-bromo-2-methylbutanal?</strong> A)   B)   C)   D)
D) <strong>Which is the structure of 3-bromo-2-methylbutanal?</strong> A)   B)   C)   D)
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18
What is the IUPAC name of the compound shown below? <strong>What is the IUPAC name of the compound shown below?  </strong> A)1-pentanone B)Cyclopentanone C)Phenone D)Cyclopentone

A)1-pentanone
B)Cyclopentanone
C)Phenone
D)Cyclopentone
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19
What is the structure of 2-ethyl-4-methyloctanal?

A) <strong>What is the structure of 2-ethyl-4-methyloctanal?</strong> A)   B)   C)   D)
B) <strong>What is the structure of 2-ethyl-4-methyloctanal?</strong> A)   B)   C)   D)
C) <strong>What is the structure of 2-ethyl-4-methyloctanal?</strong> A)   B)   C)   D)
D) <strong>What is the structure of 2-ethyl-4-methyloctanal?</strong> A)   B)   C)   D)
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20
Which compound could be oxidized to form the carboxylic acid below? <strong>Which compound could be oxidized to form the carboxylic acid below?  </strong> A)CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CHO B)   C)   D)

A)CH3(CH2)5CHO
B) <strong>Which compound could be oxidized to form the carboxylic acid below?  </strong> A)CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CHO B)   C)   D)
C) <strong>Which compound could be oxidized to form the carboxylic acid below?  </strong> A)CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CHO B)   C)   D)
D) <strong>Which compound could be oxidized to form the carboxylic acid below?  </strong> A)CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CHO B)   C)   D)
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21
What hemiacetal is formed in the reaction below? <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)

A) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)
B) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)
C) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)
D) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)
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22
What is the acetal formed in the reaction below,if two equivalents of alcohol are used? <strong>What is the acetal formed in the reaction below,if two equivalents of alcohol are used?  </strong> A)   B)   C)   D)

A) <strong>What is the acetal formed in the reaction below,if two equivalents of alcohol are used?  </strong> A)   B)   C)   D)
B) <strong>What is the acetal formed in the reaction below,if two equivalents of alcohol are used?  </strong> A)   B)   C)   D)
C) <strong>What is the acetal formed in the reaction below,if two equivalents of alcohol are used?  </strong> A)   B)   C)   D)
D) <strong>What is the acetal formed in the reaction below,if two equivalents of alcohol are used?  </strong> A)   B)   C)   D)
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23
What product is formed when the following molecule is treated with H2 and a Pd catalyst? <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)

A) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)
B) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)
C) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)
D) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)
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24
Which reactant would be needed to form the alcohol product CH3CH2CH2OH by a reduction reaction?

A) <strong>Which reactant would be needed to form the alcohol product CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH by a reduction reaction?</strong> A)   B)   C)   D)
B) <strong>Which reactant would be needed to form the alcohol product CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH by a reduction reaction?</strong> A)   B)   C)   D)
C) <strong>Which reactant would be needed to form the alcohol product CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH by a reduction reaction?</strong> A)   B)   C)   D)
D) <strong>Which reactant would be needed to form the alcohol product CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH by a reduction reaction?</strong> A)   B)   C)   D)
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25
What hemiacetal is formed in the reaction below? <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)

A) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)
B) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)
C) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)
D) <strong>What hemiacetal is formed in the reaction below?  </strong> A)   B)   C)   D)
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26
Which compound is a hemiacetal?

A) <strong>Which compound is a hemiacetal?</strong> A)   B)   C)   D)   E)
B) <strong>Which compound is a hemiacetal?</strong> A)   B)   C)   D)   E)
C) <strong>Which compound is a hemiacetal?</strong> A)   B)   C)   D)   E)
D) <strong>Which compound is a hemiacetal?</strong> A)   B)   C)   D)   E)
E) <strong>Which compound is a hemiacetal?</strong> A)   B)   C)   D)   E)
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27
What reaction does the coenzyme NADH,in the presence of an enzyme,facilitate?

A)The reduction of a carbonyl group to form a carboxylic acid
B)The reduction of a carbonyl group to form an alcohol
C)The reduction of a carboxylic acid to form a carbonyl group
D)The oxidation of a carbonyl group to form an alcohol
E)The oxidation of a carbonyl group to form a carboxylic acid
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28
Which compound is an acetal?

A) <strong>Which compound is an acetal?</strong> A)   B)   C)   D)   E)
B) <strong>Which compound is an acetal?</strong> A)   B)   C)   D)   E)
C) <strong>Which compound is an acetal?</strong> A)   B)   C)   D)   E)
D) <strong>Which compound is an acetal?</strong> A)   B)   C)   D)   E)
E) <strong>Which compound is an acetal?</strong> A)   B)   C)   D)   E)
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29
What product is formed when the compound shown below is treated with Tollens reagent? <strong>What product is formed when the compound shown below is treated with Tollens reagent?  </strong> A)   B)   C)   D)

A) <strong>What product is formed when the compound shown below is treated with Tollens reagent?  </strong> A)   B)   C)   D)
B) <strong>What product is formed when the compound shown below is treated with Tollens reagent?  </strong> A)   B)   C)   D)
C) <strong>What product is formed when the compound shown below is treated with Tollens reagent?  </strong> A)   B)   C)   D)
D) <strong>What product is formed when the compound shown below is treated with Tollens reagent?  </strong> A)   B)   C)   D)
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30
The compound below is classified as what type of compound? <strong>The compound below is classified as what type of compound?  </strong> A)An acetal B)A hemiacetal C)An ether D)An acetal and an ether

A)An acetal
B)A hemiacetal
C)An ether
D)An acetal and an ether
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31
The compound below is classified as what type of compound? <strong>The compound below is classified as what type of compound?  </strong> A)An acetal B)A hemiacetal C)An ether D)A cyclic acetal E)An acetal and an ether

A)An acetal
B)A hemiacetal
C)An ether
D)A cyclic acetal
E)An acetal and an ether
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32
What is the product of the reduction of a ketone?

A)A primary alcohol
B)A secondary alcohol
C)A tertiary alcohol
D)A carboxylic acid
E)An ether
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33
Which reactant would be needed to form the alcohol product shown below by a reduction reaction? <strong>Which reactant would be needed to form the alcohol product shown below by a reduction reaction?  </strong> A)   B)   C)   D)

A) <strong>Which reactant would be needed to form the alcohol product shown below by a reduction reaction?  </strong> A)   B)   C)   D)
B) <strong>Which reactant would be needed to form the alcohol product shown below by a reduction reaction?  </strong> A)   B)   C)   D)
C) <strong>Which reactant would be needed to form the alcohol product shown below by a reduction reaction?  </strong> A)   B)   C)   D)
D) <strong>Which reactant would be needed to form the alcohol product shown below by a reduction reaction?  </strong> A)   B)   C)   D)
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34
What product is formed when the following molecule is treated with H2 and a Pd catalyst? <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)

A) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)
B) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)
C) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)
D) <strong>What product is formed when the following molecule is treated with H<sub>2</sub> and a Pd catalyst?  </strong> A)   B)   C)   D)
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35
What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized? <strong>What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized?  </strong> A)   B)   C)   D)

A) <strong>What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized?  </strong> A)   B)   C)   D)
B) <strong>What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized?  </strong> A)   B)   C)   D)
C) <strong>What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized?  </strong> A)   B)   C)   D)
D) <strong>What hemiacetal is formed when the hydroxyl aldehyde shown below is cyclized?  </strong> A)   B)   C)   D)
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36
What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH3CH2OH)in the presences of H2SO4? <strong>What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)in the presences of H<sub>2</sub>SO<sub>4</sub>?  </strong> A)   B)   C)   D)

A) <strong>What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)in the presences of H<sub>2</sub>SO<sub>4</sub>?  </strong> A)   B)   C)   D)
B) <strong>What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)in the presences of H<sub>2</sub>SO<sub>4</sub>?  </strong> A)   B)   C)   D)
C) <strong>What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)in the presences of H<sub>2</sub>SO<sub>4</sub>?  </strong> A)   B)   C)   D)
D) <strong>What acetal is formed when the compound shown below is treated with two equivalents of ethanol (CH<sub>3</sub>CH<sub>2</sub>OH)in the presences of H<sub>2</sub>SO<sub>4</sub>?  </strong> A)   B)   C)   D)
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37
What is the product of the reduction of an aldehyde?

A)A primary alcohol
B)A secondary alcohol
C)A tertiary alcohol
D)A carboxylic acid
E)An ether
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38
What products are formed when the acetal below is hydrolyzed with water and sulfuric acid? <strong>What products are formed when the acetal below is hydrolyzed with water and sulfuric acid?  </strong> A)   B)   C)HOCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> + 2 CH<sub>3</sub>OH D)

A) <strong>What products are formed when the acetal below is hydrolyzed with water and sulfuric acid?  </strong> A)   B)   C)HOCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> + 2 CH<sub>3</sub>OH D)
B) <strong>What products are formed when the acetal below is hydrolyzed with water and sulfuric acid?  </strong> A)   B)   C)HOCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> + 2 CH<sub>3</sub>OH D)
C)HOCH2CH2CH2CH2CH3 + 2 CH3OH
D) <strong>What products are formed when the acetal below is hydrolyzed with water and sulfuric acid?  </strong> A)   B)   C)HOCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> + 2 CH<sub>3</sub>OH D)
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39
A hemiacetal contains which two groups bonded to the same carbon atom?

A)An OH (hydroxyl)group and an OR (alkoxy)group
B)Two OH (hydroxyl)groups
C)Two OR (alkoxy)groups
D)An OH (hydroxyl)group and a C=O (carbonyl)group
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40
Which reagent can be used to reduce a ketone?

A)K2Cr2O7
B)H2SO4
C)H2 with Pd metal
D)Ag2O in aqueous NH4OH
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41
The following ketones play an important role in the tanning industry and are found in many commercial sunscreens. Which ketone is expected to be the most soluble in water and therefore the most readily washed off when an individual goes swimming?

A) <strong>The following ketones play an important role in the tanning industry and are found in many commercial sunscreens. Which ketone is expected to be the most soluble in water and therefore the most readily washed off when an individual goes swimming?</strong> A)   B)   C)   D)All would be expected to have the same solubility.
B) <strong>The following ketones play an important role in the tanning industry and are found in many commercial sunscreens. Which ketone is expected to be the most soluble in water and therefore the most readily washed off when an individual goes swimming?</strong> A)   B)   C)   D)All would be expected to have the same solubility.
C) <strong>The following ketones play an important role in the tanning industry and are found in many commercial sunscreens. Which ketone is expected to be the most soluble in water and therefore the most readily washed off when an individual goes swimming?</strong> A)   B)   C)   D)All would be expected to have the same solubility.
D)All would be expected to have the same solubility.
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42
What product results when cinnamaldehyde is reduced with excess H2 in the presence of a Pd catalyst? <strong>What product results when cinnamaldehyde is reduced with excess H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)

A) <strong>What product results when cinnamaldehyde is reduced with excess H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)
B) <strong>What product results when cinnamaldehyde is reduced with excess H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)
C) <strong>What product results when cinnamaldehyde is reduced with excess H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)
D) <strong>What product results when cinnamaldehyde is reduced with excess H<sub>2</sub> in the presence of a Pd catalyst?  </strong> A)   B)   C)   D)
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43
What is the IUPAC name of the compound below? <strong>What is the IUPAC name of the compound below?  </strong> A)4-chloro-3-pentyl-1-cyclohexone B)4-chloro-3-pentylcyclohexanone C)1-chloro-2-pentyl-4-cyclohexanone D)4-chloro-3-pentylphenone

A)4-chloro-3-pentyl-1-cyclohexone
B)4-chloro-3-pentylcyclohexanone
C)1-chloro-2-pentyl-4-cyclohexanone
D)4-chloro-3-pentylphenone
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44
The compound butanone does not need a number to specify the location of the carbonyl group on the carbon chain. Which statement best explains why?

A)The C=O is assumed to be on C-1 of the carbon chain if it is not specified.
B)The C=O can only be on C-2 of the carbon chain in this compound.
C)The location of the C=O does not need to be specified for a cyclic ketone.
D)The C=O is on an end carbon of the carbon chain.
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45
The compound decanal contributes to the odor and flavor of an orange. Which of the statements concerning the structure of decanal is incorrect?

A)Decanal is an aldehyde.
B)Decanal contains a saturated chain of ten carbons.
C)Decanal contains a carbonyl group on the first carbon of the carbon chain.
D)Decanal is an aromatic compound.
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46
What hydrolysis products are formed when the acetal (CH3CH2CH2)2C(OCH2CH3)2 is treated with H2SO4 in H2O?

A)(CH3CH2CH2)2CHOCH2CH3 + CH3CH2OH
B)(CH3CH2CH2)2CO + 2 CH3CH2OH
C)(CH3CH2CH2)2CHOH + 2 CH3CH2OH
D)CH2(OCH2CH3)2 + 2 CH3CH2CH3
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47
Deoxyribose is a building block of DNA. Which statement concerning the functional groups present in deoxyribose,shown below,is incorrect? <strong>Deoxyribose is a building block of DNA. Which statement concerning the functional groups present in deoxyribose,shown below,is incorrect?  </strong> A)It contains an acetal. B)It contains an alcohol. C)It contains a hemiacetal. D)None of these choices are incorrect.

A)It contains an acetal.
B)It contains an alcohol.
C)It contains a hemiacetal.
D)None of these choices are incorrect.
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48
What is the name of the compound below? <strong>What is the name of the compound below?  </strong> A)3-bromo-4-ethyl-2-methylbenzaldehyde B)3-bromo-4-ethoxy-2-methoxybenzaldehyde C)1-bromo-2-ethoxy-6-methoxy-3-benzaldehyde D)3-bromo-4-ethoxy-2-methoxyphenal

A)3-bromo-4-ethyl-2-methylbenzaldehyde
B)3-bromo-4-ethoxy-2-methoxybenzaldehyde
C)1-bromo-2-ethoxy-6-methoxy-3-benzaldehyde
D)3-bromo-4-ethoxy-2-methoxyphenal
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49
What type of compound is shown below? <strong>What type of compound is shown below?  </strong> A)An epoxide B)A cyclic hemiacetal C)An aldehyde D)A cyclic acetal

A)An epoxide
B)A cyclic hemiacetal
C)An aldehyde
D)A cyclic acetal
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50
What is the structure of 2-bromo-5-hydroxyheptanal?

A) <strong>What is the structure of 2-bromo-5-hydroxyheptanal?</strong> A)   B)   C)   D)
B) <strong>What is the structure of 2-bromo-5-hydroxyheptanal?</strong> A)   B)   C)   D)
C) <strong>What is the structure of 2-bromo-5-hydroxyheptanal?</strong> A)   B)   C)   D)
D) <strong>What is the structure of 2-bromo-5-hydroxyheptanal?</strong> A)   B)   C)   D)
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51
Salicin is a naturally occurring pain reliever isolated from the bark of willow trees. Which statement concerning the functional groups present in salicin is incorrect? <strong>Salicin is a naturally occurring pain reliever isolated from the bark of willow trees. Which statement concerning the functional groups present in salicin is incorrect?  </strong> A)It contains an acetal. B)It contains an alcohol. C)It contains a hemiacetal. D)It contains a phenol.

A)It contains an acetal.
B)It contains an alcohol.
C)It contains a hemiacetal.
D)It contains a phenol.
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52
Which of the following is the product of the reduction of acetone,shown below? <strong>Which of the following is the product of the reduction of acetone,shown below?  </strong> A)   B)   C)   D)

A) <strong>Which of the following is the product of the reduction of acetone,shown below?  </strong> A)   B)   C)   D)
B) <strong>Which of the following is the product of the reduction of acetone,shown below?  </strong> A)   B)   C)   D)
C) <strong>Which of the following is the product of the reduction of acetone,shown below?  </strong> A)   B)   C)   D)
D) <strong>Which of the following is the product of the reduction of acetone,shown below?  </strong> A)   B)   C)   D)
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53
What product results when cinnamaldehyde is oxidized? <strong>What product results when cinnamaldehyde is oxidized?  </strong> A)   B)   C)   D)

A) <strong>What product results when cinnamaldehyde is oxidized?  </strong> A)   B)   C)   D)
B) <strong>What product results when cinnamaldehyde is oxidized?  </strong> A)   B)   C)   D)
C) <strong>What product results when cinnamaldehyde is oxidized?  </strong> A)   B)   C)   D)
D) <strong>What product results when cinnamaldehyde is oxidized?  </strong> A)   B)   C)   D)
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54
In the correct order,what are the three reactions that convert all-trans-retinal into 11-cis-retinal so that the process of vision can continue?

A)Reduction,Oxidation,Isomerization
B)Reduction,Isomerization,Oxidation
C)Oxidation,Isomerization,Reduction
D)Oxidation,Reduction,Isomerization
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55
What is the name of the compound below? <strong>What is the name of the compound below?  </strong> A)1-methoxy-3-methylbenzene B)4-methoxy-6-methylbenzaldehyde C)4-methoxy-2-methylacetophenone D)5-methoxy-3-methyltoluene

A)1-methoxy-3-methylbenzene
B)4-methoxy-6-methylbenzaldehyde
C)4-methoxy-2-methylacetophenone
D)5-methoxy-3-methyltoluene
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56
What type of compound is shown below? <strong>What type of compound is shown below?  </strong> A)An epoxide B)A cyclic hemiacetal C)An aldehyde D)A cyclic acetal

A)An epoxide
B)A cyclic hemiacetal
C)An aldehyde
D)A cyclic acetal
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57
What is the name of the compound below? <strong>What is the name of the compound below?  </strong> A)3-chlorobenzenal B)3-methanalchlorobenzene C)M-chlorobenzaldehyde D)P-chloroacetophenone

A)3-chlorobenzenal
B)3-methanalchlorobenzene
C)M-chlorobenzaldehyde
D)P-chloroacetophenone
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58
What is the name of the compound below? <strong>What is the name of the compound below?  </strong> A)2-ethylbenzenone B)2-ethylacetophenone C)2-ethylacetobenzone D)2-ethylphenone

A)2-ethylbenzenone
B)2-ethylacetophenone
C)2-ethylacetobenzone
D)2-ethylphenone
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59
What is the structure of 3-hydroxy-2-methylbenzaldehyde?

A) <strong>What is the structure of 3-hydroxy-2-methylbenzaldehyde?</strong> A)   B)   C)   D)
B) <strong>What is the structure of 3-hydroxy-2-methylbenzaldehyde?</strong> A)   B)   C)   D)
C) <strong>What is the structure of 3-hydroxy-2-methylbenzaldehyde?</strong> A)   B)   C)   D)
D) <strong>What is the structure of 3-hydroxy-2-methylbenzaldehyde?</strong> A)   B)   C)   D)
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60
The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction? <strong>The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction?  </strong> A)   B)   C)   D)

A) <strong>The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction?  </strong> A)   B)   C)   D)
B) <strong>The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction?  </strong> A)   B)   C)   D)
C) <strong>The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction?  </strong> A)   B)   C)   D)
D) <strong>The reduction of acetaldehyde is an important biochemical reaction. Which of the following is the product of its reduction?  </strong> A)   B)   C)   D)
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61
The reaction below illustrates oxidation of an aldehyde. The reaction below illustrates oxidation of an aldehyde.
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62
When light hits the retina,the 11-cis double bond of 11-cis-retinal is isomerized to its more stable trans isomer,and the all-trans-retinal is formed.
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63
The reaction below illustrates oxidation by Tollens reagent. The reaction below illustrates oxidation by Tollens reagent.
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64
Ketones are not oxidized since they contain no H atom bonded to the carbonyl carbon.
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65
Vanillin,acetone,and formaldehyde are aldehydes.
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66
The reaction below illustrates oxidation by Tollens' reagent. The reaction below illustrates oxidation by Tollens' reagent.
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67
When the hemiacetal below reacts with ethanol,what acetal is formed? <strong>When the hemiacetal below reacts with ethanol,what acetal is formed?  </strong> A)   B)   C)   D)

A) <strong>When the hemiacetal below reacts with ethanol,what acetal is formed?  </strong> A)   B)   C)   D)
B) <strong>When the hemiacetal below reacts with ethanol,what acetal is formed?  </strong> A)   B)   C)   D)
C) <strong>When the hemiacetal below reacts with ethanol,what acetal is formed?  </strong> A)   B)   C)   D)
D) <strong>When the hemiacetal below reacts with ethanol,what acetal is formed?  </strong> A)   B)   C)   D)
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68
The structure below contains both an acetal and hemiacetal. The structure below contains both an acetal and hemiacetal.
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69
Triamcinolone acetonide (structure shown),a synthetic corticosteroid drug,contains an acetal. Triamcinolone acetonide (structure shown),a synthetic corticosteroid drug,contains an acetal.
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70
4,4-Dimethyl-2-hexanone is a ketone of molecular formula C8H16O that has six carbons in its longest chain.
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71
The carbohydrate glucose exists predominantly as a cyclic hemiacetal.
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72
11-cis-retinal is a ketone in the rod cells of the eye that is critical for vision.
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73
Acetals are stable molecules,but they can be converted back to aldehydes and ketones by treatment with acid and water.
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74
Acetals are ethers.
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75
Cyclic hemiacetals are converted to acetals by reaction with an alcohol.
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76
Aldehydes and ketones undergo addition reactions with alcohols (ROH)to form hemiacetals and acetals.
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77
Aldehydes and ketones undergo addition reactions with alcohols (ROH)to form hemiacetals and acetals.
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78
As is in the laboratory,the reduction of carbonyl groups in biological systems is accomplished using H2 and Pd as a reducing agent.
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79
D-Glucose,shown below,will give a positive Tollens test. D-Glucose,shown below,will give a positive Tollens test.
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80
The compound below is an acetal. The compound below is an acetal.
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