Deck 15: Carboxylic Acids and Their Derivatives-Nucleophilic Acyl Substitution
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Deck 15: Carboxylic Acids and Their Derivatives-Nucleophilic Acyl Substitution
1
Will the following reaction occur?


True
2
What is the product of the following reaction? 
A) IV
B) II
C) I
D) III

A) IV
B) II
C) I
D) III
II
3
What is the product of the following reaction? 
A) III
B) I
C) II
D) IV

A) III
B) I
C) II
D) IV
IV
4
What is the product of the following reaction? 
A) I
B) III
C) II
D) IV

A) I
B) III
C) II
D) IV
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5
What is the missing reagent in the reaction below? 
A) SOCl2
B) Acetic acid
C) NaOMe
D) Pyridine

A) SOCl2
B) Acetic acid
C) NaOMe
D) Pyridine
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6
Give the IUPAC name for the following compound. 
A) 3-hexanoate
B) 4-hexanoate
C) Butyl ethanoate
D) Ethyl butanoate

A) 3-hexanoate
B) 4-hexanoate
C) Butyl ethanoate
D) Ethyl butanoate
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7
What is the product of the following reaction? 
A) III
B) IV
C) I
D) II

A) III
B) IV
C) I
D) II
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8
Acetyl coenzyme A is commonly used to perform the following type of organic reaction:
A) Wittig reaction
B) Acyl transfer reaction
C) Reduction
D) Oxidation
A) Wittig reaction
B) Acyl transfer reaction
C) Reduction
D) Oxidation
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9
How can you convert a carboxylic acid into an acid chloride?
A) React with Cl2 and FeCl3.
B) Heat with hydrochloric acid.
C) React with sodium chloride.
D) React with thionyl chloride (SOCl2).
A) React with Cl2 and FeCl3.
B) Heat with hydrochloric acid.
C) React with sodium chloride.
D) React with thionyl chloride (SOCl2).
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10
What is the product of the following reaction? 
A) IV
B) I
C) III
D) II

A) IV
B) I
C) III
D) II
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11
What is the IUPAC name for the following compound? 
A) Phenyl acetate
B) Phenyl propanoate
C) Propionyl phenol
D) Phenol propanoate

A) Phenyl acetate
B) Phenyl propanoate
C) Propionyl phenol
D) Phenol propanoate
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12
Which of the following peaks would you see in the IR spectrum of a carboxylic acid?
A) A sharp line at 2250 cm-1
B) A broad peak from 800-600 cm-1
C) A flat line (carboxylic acids are not IR active)
D) A broad peak from 3800-2800 cm-1
A) A sharp line at 2250 cm-1
B) A broad peak from 800-600 cm-1
C) A flat line (carboxylic acids are not IR active)
D) A broad peak from 3800-2800 cm-1
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13
Which of the following statements about amides is true?
A) Amides are hydrolyzed in acid or base to form carboxylic acids or carboxylate anions.
B) Amides do not react under any conditions. They are inert compounds.
C) Amides react with thionyl chloride to form the acid chloride.
D) Amides react with methyl alcohol in the presence of an acid catalyst to form an ester.
A) Amides are hydrolyzed in acid or base to form carboxylic acids or carboxylate anions.
B) Amides do not react under any conditions. They are inert compounds.
C) Amides react with thionyl chloride to form the acid chloride.
D) Amides react with methyl alcohol in the presence of an acid catalyst to form an ester.
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14
What reagent(s) would be needed to complete the following organic reaction?
I. CH3NH2
II. NH4Cl
III. NH3
IV. H2O

A) III
B) II
C) I
D) IV
I. CH3NH2
II. NH4Cl
III. NH3
IV. H2O

A) III
B) II
C) I
D) IV
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15
Will the following reaction occur?


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16
What is the product of the following reaction? 
A) I
B) III
C) II
D) IV

A) I
B) III
C) II
D) IV
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17
What is the product of the following reaction? 
A) I
B) III
C) IV
D) II

A) I
B) III
C) IV
D) II
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18
Will the following reaction occur?


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19
What is the product of the following reaction? 
A) II
B) I
C) III
D) IV

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