Deck 23: Ester Enolates and the Claisen Condensation: Synthesis of B-Dicarbonyl Compounds; Acyl Anion Equivalents

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Question
What missing reactant would be required to provide the product shown? <strong>What missing reactant would be required to provide the product shown?  </strong> A)   B)   C)   D)   E) None of these would work. <div style=padding-top: 35px>

A)
<strong>What missing reactant would be required to provide the product shown?  </strong> A)   B)   C)   D)   E) None of these would work. <div style=padding-top: 35px>
B)
<strong>What missing reactant would be required to provide the product shown?  </strong> A)   B)   C)   D)   E) None of these would work. <div style=padding-top: 35px>
C)
<strong>What missing reactant would be required to provide the product shown?  </strong> A)   B)   C)   D)   E) None of these would work. <div style=padding-top: 35px>
D)
<strong>What missing reactant would be required to provide the product shown?  </strong> A)   B)   C)   D)   E) None of these would work. <div style=padding-top: 35px>
E) None of these would work.
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Question
Which of the following would be the most acidic?

A)
<strong>Which of the following would be the most acidic?</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>CH<sub>3</sub> C)   D)   E)   <div style=padding-top: 35px>
B) CH3CH2CO2CH3
C)
<strong>Which of the following would be the most acidic?</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>CH<sub>3</sub> C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following would be the most acidic?</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>CH<sub>3</sub> C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following would be the most acidic?</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>CH<sub>3</sub> C)   D)   E)   <div style=padding-top: 35px>
Question
What problem is encountered in the synthesis of ethyl acetoacetate (shown below)if sodium methoxide is used rather than sodium ethoxide? <strong>What problem is encountered in the synthesis of ethyl acetoacetate (shown below)if sodium methoxide is used rather than sodium ethoxide?  </strong> A) Sodium methoxide is too weak a base to cause this reaction to occur. B) The condensation proceeds further to give tri-carbonyl products. C) The reaction would produce some of both the methyl ester and the ethyl ester. D) Sodium methoxide is too insoluble in methanol to promote the reaction. E) Sodium methoxide is not basic enough to drive the reaction to completion. <div style=padding-top: 35px>

A) Sodium methoxide is too weak a base to cause this reaction to occur.
B) The condensation proceeds further to give tri-carbonyl products.
C) The reaction would produce some of both the methyl ester and the ethyl ester.
D) Sodium methoxide is too insoluble in methanol to promote the reaction.
E) Sodium methoxide is not basic enough to drive the reaction to completion.
Question
Which of the following reaction sequences will affect the following transformation? <strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What product would be expected to result from the reaction sequence shown? <strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What would be the expected product of the following reaction sequence? <strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Predict the products of the following reaction. <strong>Predict the products of the following reaction.  </strong> A)   B)   C)   D)   E) None of these. <div style=padding-top: 35px>

A)
<strong>Predict the products of the following reaction.  </strong> A)   B)   C)   D)   E) None of these. <div style=padding-top: 35px>
B)
<strong>Predict the products of the following reaction.  </strong> A)   B)   C)   D)   E) None of these. <div style=padding-top: 35px>
C)
<strong>Predict the products of the following reaction.  </strong> A)   B)   C)   D)   E) None of these. <div style=padding-top: 35px>
D)
<strong>Predict the products of the following reaction.  </strong> A)   B)   C)   D)   E) None of these. <div style=padding-top: 35px>
E) None of these.
Question
Predict the major product of the following reaction? <strong>Predict the major product of the following reaction?  </strong> A)   B)   C)   D)   E) No significant reaction occurs. <div style=padding-top: 35px>

A)
<strong>Predict the major product of the following reaction?  </strong> A)   B)   C)   D)   E) No significant reaction occurs. <div style=padding-top: 35px>
B)
<strong>Predict the major product of the following reaction?  </strong> A)   B)   C)   D)   E) No significant reaction occurs. <div style=padding-top: 35px>
C)
<strong>Predict the major product of the following reaction?  </strong> A)   B)   C)   D)   E) No significant reaction occurs. <div style=padding-top: 35px>
D)
<strong>Predict the major product of the following reaction?  </strong> A)   B)   C)   D)   E) No significant reaction occurs. <div style=padding-top: 35px>
E) No significant reaction occurs.
Question
What factors contribute to the stability of the following structure? <strong>What factors contribute to the stability of the following structure?  </strong> A) structure has a 6<font face=symbol></font> electron aromatic system B) stabilized by conjugation between C=C and C=O C) C=C is generally more stable than C=O D) structure has intramolecular hydrogen bonding E) More than one of the above are true. <div style=padding-top: 35px>

A) structure has a 6 electron aromatic system
B) stabilized by conjugation between C=C and C=O
C) C=C is generally more stable than C=O
D) structure has intramolecular hydrogen bonding
E) More than one of the above are true.
Question
What would result from the reaction shown below? <strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following compounds will not readily undergo decarboxylation (loss of CO2)upon heating in an appropriate solvent?

A)
<strong>Which of the following compounds will not readily undergo decarboxylation (loss of CO<sub>2</sub>)upon heating in an appropriate solvent?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following compounds will not readily undergo decarboxylation (loss of CO<sub>2</sub>)upon heating in an appropriate solvent?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following compounds will not readily undergo decarboxylation (loss of CO<sub>2</sub>)upon heating in an appropriate solvent?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following compounds will not readily undergo decarboxylation (loss of CO<sub>2</sub>)upon heating in an appropriate solvent?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following compounds will not readily undergo decarboxylation (loss of CO<sub>2</sub>)upon heating in an appropriate solvent?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What product would result from the following reaction sequence? <strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Predict the major organic product of the following reaction. <strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E) The reaction does not occur. <div style=padding-top: 35px>

A)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E) The reaction does not occur. <div style=padding-top: 35px>
B)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E) The reaction does not occur. <div style=padding-top: 35px>
C)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E) The reaction does not occur. <div style=padding-top: 35px>
D)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E) The reaction does not occur. <div style=padding-top: 35px>
E) The reaction does not occur.
Question
Predict the major product of the following reaction. <strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The Dieckmann reaction is best described by which of the following statements?

A) Intermolecular Aldol Condensation
B) Intramolecular Aldol Condensation
C) Intermolecular Claisen Condensation
D) Intramolecular Claisen Condensation
E) Michael Addition followed by intramolecular Aldol
Question
To which side,if any,would the following equilibrium lie? <strong>To which side,if any,would the following equilibrium lie?  </strong> A) To the left B) To the right C) Equally to the left and right D) Reaction cannot occur at all E) Equilibrium favors a different product <div style=padding-top: 35px>

A) To the left
B) To the right
C) Equally to the left and right
D) Reaction cannot occur at all
E) Equilibrium favors a different product
Question
Why is the following reaction typically done? <strong>Why is the following reaction typically done?  </strong> A) To protect the aldehyde against oxidation B) To render the molecule inert to organometallic reagents C) To make the aldehyde CH more acidic D) To render the molecule more fragrant E) To protect the aldehyde against reduction <div style=padding-top: 35px>

A) To protect the aldehyde against oxidation
B) To render the molecule inert to organometallic reagents
C) To make the aldehyde CH more acidic
D) To render the molecule more fragrant
E) To protect the aldehyde against reduction
Question
What would be the organic product of the following reaction? <strong>What would be the organic product of the following reaction?  </strong> A) 2 HO<sub>2</sub>CCH<sub>2</sub>CO<sub>2</sub>H B) 2 CH<sub>3</sub>C(=O)CH<sub>3</sub> C) 2 CH<sub>3</sub>CO<sub>2</sub>H D) HO<sub>2</sub>CCH<sub>2</sub>C(=O)O<sub>2</sub>CCH<sub>2</sub>C(=O)O<sub>2</sub>CCH<sub>2</sub>CO<sub>2</sub>H E) No reaction occurs. <div style=padding-top: 35px>

A) 2 HO2CCH2CO2H
B) 2 CH3C(=O)CH3
C) 2 CH3CO2H
D) HO2CCH2C(=O)O2CCH2C(=O)O2CCH2CO2H
E) No reaction occurs.
Question
Predict the major product of the following reaction. <strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Predict the major organic product of the following reaction. <strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following processes involves loss of one carbon as carbon dioxide?

A) Claisen condensation
B) Michael addition
C) Malonic ester synthesis
D) None involve loss of CO2.
E) All involve loss of CO2.
Question
Which of the indicated hydrogens would be the most acidic? <strong>Which of the indicated hydrogens would be the most acidic?  </strong> A) Hydrogens a B) Hydrogens b C) Hydrogens c D) Hydrogens d E) Hydrogens e <div style=padding-top: 35px>

A) Hydrogens a
B) Hydrogens b
C) Hydrogens c
D) Hydrogens d
E) Hydrogens e
Question
What product do you expect from the following reaction? <strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
After treatment with aqueous base + heat,followed by acidification to pH 2 followed by heating,which carbon in the molecule below would be lost as carbon dioxide? <strong>After treatment with aqueous base + heat,followed by acidification to pH 2 followed by heating,which carbon in the molecule below would be lost as carbon dioxide?  </strong> A) Carbon a B) Carbon b C) Carbon c D) Carbon d E) Carbon e <div style=padding-top: 35px>

A) Carbon a
B) Carbon b
C) Carbon c
D) Carbon d
E) Carbon e
Question
What product do you expect from the following reaction? <strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>

A)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
B)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
C)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
D)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
E) no reaction
Question
What product do you expect from the following reaction? <strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What product do you expect from the following reaction? <strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D) Some of these would be formed. E) None of these would be formed. <div style=padding-top: 35px>

A)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D) Some of these would be formed. E) None of these would be formed. <div style=padding-top: 35px>
B)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D) Some of these would be formed. E) None of these would be formed. <div style=padding-top: 35px>
C)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D) Some of these would be formed. E) None of these would be formed. <div style=padding-top: 35px>
D) Some of these would be formed.
E) None of these would be formed.
Question
Which would be the most acidic proton in the molecule below? <strong>Which would be the most acidic proton in the molecule below?  </strong> A) Protons a B) Proton b C) Proton c D) Protons d E) Protons e <div style=padding-top: 35px>

A) Protons a
B) Proton b
C) Proton c
D) Protons d
E) Protons e
Question
What would be the expected product of the following reaction sequence? <strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
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Deck 23: Ester Enolates and the Claisen Condensation: Synthesis of B-Dicarbonyl Compounds; Acyl Anion Equivalents
1
What missing reactant would be required to provide the product shown? <strong>What missing reactant would be required to provide the product shown?  </strong> A)   B)   C)   D)   E) None of these would work.

A)
<strong>What missing reactant would be required to provide the product shown?  </strong> A)   B)   C)   D)   E) None of these would work.
B)
<strong>What missing reactant would be required to provide the product shown?  </strong> A)   B)   C)   D)   E) None of these would work.
C)
<strong>What missing reactant would be required to provide the product shown?  </strong> A)   B)   C)   D)   E) None of these would work.
D)
<strong>What missing reactant would be required to provide the product shown?  </strong> A)   B)   C)   D)   E) None of these would work.
E) None of these would work.
2
Which of the following would be the most acidic?

A)
<strong>Which of the following would be the most acidic?</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>CH<sub>3</sub> C)   D)   E)
B) CH3CH2CO2CH3
C)
<strong>Which of the following would be the most acidic?</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>CH<sub>3</sub> C)   D)   E)
D)
<strong>Which of the following would be the most acidic?</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>CH<sub>3</sub> C)   D)   E)
E)
<strong>Which of the following would be the most acidic?</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>CH<sub>3</sub> C)   D)   E)
3
What problem is encountered in the synthesis of ethyl acetoacetate (shown below)if sodium methoxide is used rather than sodium ethoxide? <strong>What problem is encountered in the synthesis of ethyl acetoacetate (shown below)if sodium methoxide is used rather than sodium ethoxide?  </strong> A) Sodium methoxide is too weak a base to cause this reaction to occur. B) The condensation proceeds further to give tri-carbonyl products. C) The reaction would produce some of both the methyl ester and the ethyl ester. D) Sodium methoxide is too insoluble in methanol to promote the reaction. E) Sodium methoxide is not basic enough to drive the reaction to completion.

A) Sodium methoxide is too weak a base to cause this reaction to occur.
B) The condensation proceeds further to give tri-carbonyl products.
C) The reaction would produce some of both the methyl ester and the ethyl ester.
D) Sodium methoxide is too insoluble in methanol to promote the reaction.
E) Sodium methoxide is not basic enough to drive the reaction to completion.
The reaction would produce some of both the methyl ester and the ethyl ester.
4
Which of the following reaction sequences will affect the following transformation? <strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)

A)
<strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following reaction sequences will affect the following transformation?  </strong> A)   B)   C)   D)   E)
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5
What product would be expected to result from the reaction sequence shown? <strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)

A)
<strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)
B)
<strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)
C)
<strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)
D)
<strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)
E)
<strong>What product would be expected to result from the reaction sequence shown?  </strong> A)   B)   C)   D)   E)
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6
What would be the expected product of the following reaction sequence? <strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)

A)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)
B)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)
C)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)
D)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)
E)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)
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7
Predict the products of the following reaction. <strong>Predict the products of the following reaction.  </strong> A)   B)   C)   D)   E) None of these.

A)
<strong>Predict the products of the following reaction.  </strong> A)   B)   C)   D)   E) None of these.
B)
<strong>Predict the products of the following reaction.  </strong> A)   B)   C)   D)   E) None of these.
C)
<strong>Predict the products of the following reaction.  </strong> A)   B)   C)   D)   E) None of these.
D)
<strong>Predict the products of the following reaction.  </strong> A)   B)   C)   D)   E) None of these.
E) None of these.
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8
Predict the major product of the following reaction? <strong>Predict the major product of the following reaction?  </strong> A)   B)   C)   D)   E) No significant reaction occurs.

A)
<strong>Predict the major product of the following reaction?  </strong> A)   B)   C)   D)   E) No significant reaction occurs.
B)
<strong>Predict the major product of the following reaction?  </strong> A)   B)   C)   D)   E) No significant reaction occurs.
C)
<strong>Predict the major product of the following reaction?  </strong> A)   B)   C)   D)   E) No significant reaction occurs.
D)
<strong>Predict the major product of the following reaction?  </strong> A)   B)   C)   D)   E) No significant reaction occurs.
E) No significant reaction occurs.
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9
What factors contribute to the stability of the following structure? <strong>What factors contribute to the stability of the following structure?  </strong> A) structure has a 6<font face=symbol></font> electron aromatic system B) stabilized by conjugation between C=C and C=O C) C=C is generally more stable than C=O D) structure has intramolecular hydrogen bonding E) More than one of the above are true.

A) structure has a 6 electron aromatic system
B) stabilized by conjugation between C=C and C=O
C) C=C is generally more stable than C=O
D) structure has intramolecular hydrogen bonding
E) More than one of the above are true.
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10
What would result from the reaction shown below? <strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)

A)
<strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)
B)
<strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)
C)
<strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)
D)
<strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)
E)
<strong>What would result from the reaction shown below?  </strong> A)   B)   C)   D)   E)
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11
Which of the following compounds will not readily undergo decarboxylation (loss of CO2)upon heating in an appropriate solvent?

A)
<strong>Which of the following compounds will not readily undergo decarboxylation (loss of CO<sub>2</sub>)upon heating in an appropriate solvent?</strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following compounds will not readily undergo decarboxylation (loss of CO<sub>2</sub>)upon heating in an appropriate solvent?</strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following compounds will not readily undergo decarboxylation (loss of CO<sub>2</sub>)upon heating in an appropriate solvent?</strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following compounds will not readily undergo decarboxylation (loss of CO<sub>2</sub>)upon heating in an appropriate solvent?</strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following compounds will not readily undergo decarboxylation (loss of CO<sub>2</sub>)upon heating in an appropriate solvent?</strong> A)   B)   C)   D)   E)
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12
What product would result from the following reaction sequence? <strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)

A)
<strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)
B)
<strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)
C)
<strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)
D)
<strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)
E)
<strong>What product would result from the following reaction sequence?  </strong> A)   <sup> </sup> B)   C)   D)   E)
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13
Predict the major organic product of the following reaction. <strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E) The reaction does not occur.

A)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E) The reaction does not occur.
B)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E) The reaction does not occur.
C)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E) The reaction does not occur.
D)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E) The reaction does not occur.
E) The reaction does not occur.
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14
Predict the major product of the following reaction. <strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)

A)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)
B)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)
C)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)
D)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)
E)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)
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15
The Dieckmann reaction is best described by which of the following statements?

A) Intermolecular Aldol Condensation
B) Intramolecular Aldol Condensation
C) Intermolecular Claisen Condensation
D) Intramolecular Claisen Condensation
E) Michael Addition followed by intramolecular Aldol
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16
To which side,if any,would the following equilibrium lie? <strong>To which side,if any,would the following equilibrium lie?  </strong> A) To the left B) To the right C) Equally to the left and right D) Reaction cannot occur at all E) Equilibrium favors a different product

A) To the left
B) To the right
C) Equally to the left and right
D) Reaction cannot occur at all
E) Equilibrium favors a different product
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17
Why is the following reaction typically done? <strong>Why is the following reaction typically done?  </strong> A) To protect the aldehyde against oxidation B) To render the molecule inert to organometallic reagents C) To make the aldehyde CH more acidic D) To render the molecule more fragrant E) To protect the aldehyde against reduction

A) To protect the aldehyde against oxidation
B) To render the molecule inert to organometallic reagents
C) To make the aldehyde CH more acidic
D) To render the molecule more fragrant
E) To protect the aldehyde against reduction
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18
What would be the organic product of the following reaction? <strong>What would be the organic product of the following reaction?  </strong> A) 2 HO<sub>2</sub>CCH<sub>2</sub>CO<sub>2</sub>H B) 2 CH<sub>3</sub>C(=O)CH<sub>3</sub> C) 2 CH<sub>3</sub>CO<sub>2</sub>H D) HO<sub>2</sub>CCH<sub>2</sub>C(=O)O<sub>2</sub>CCH<sub>2</sub>C(=O)O<sub>2</sub>CCH<sub>2</sub>CO<sub>2</sub>H E) No reaction occurs.

A) 2 HO2CCH2CO2H
B) 2 CH3C(=O)CH3
C) 2 CH3CO2H
D) HO2CCH2C(=O)O2CCH2C(=O)O2CCH2CO2H
E) No reaction occurs.
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19
Predict the major product of the following reaction. <strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)

A)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)
B)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)
C)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)
D)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)
E)
<strong>Predict the major product of the following reaction.  </strong> A)   B)   C)   D)   E)
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20
Predict the major organic product of the following reaction. <strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)

A)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)
B)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)
C)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)
D)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)
E)
<strong>Predict the major organic product of the following reaction.  </strong> A)   B)   C)   D)   E)
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21
Which of the following processes involves loss of one carbon as carbon dioxide?

A) Claisen condensation
B) Michael addition
C) Malonic ester synthesis
D) None involve loss of CO2.
E) All involve loss of CO2.
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22
Which of the indicated hydrogens would be the most acidic? <strong>Which of the indicated hydrogens would be the most acidic?  </strong> A) Hydrogens a B) Hydrogens b C) Hydrogens c D) Hydrogens d E) Hydrogens e

A) Hydrogens a
B) Hydrogens b
C) Hydrogens c
D) Hydrogens d
E) Hydrogens e
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23
What product do you expect from the following reaction? <strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)

A)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)
B)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)
C)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)
D)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)
E)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)
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24
After treatment with aqueous base + heat,followed by acidification to pH 2 followed by heating,which carbon in the molecule below would be lost as carbon dioxide? <strong>After treatment with aqueous base + heat,followed by acidification to pH 2 followed by heating,which carbon in the molecule below would be lost as carbon dioxide?  </strong> A) Carbon a B) Carbon b C) Carbon c D) Carbon d E) Carbon e

A) Carbon a
B) Carbon b
C) Carbon c
D) Carbon d
E) Carbon e
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25
What product do you expect from the following reaction? <strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E) no reaction

A)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E) no reaction
B)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E) no reaction
C)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E) no reaction
D)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E) no reaction
E) no reaction
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26
What product do you expect from the following reaction? <strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)

A)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)
B)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)
C)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)
D)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)
E)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D)   E)
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27
What product do you expect from the following reaction? <strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D) Some of these would be formed. E) None of these would be formed.

A)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D) Some of these would be formed. E) None of these would be formed.
B)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D) Some of these would be formed. E) None of these would be formed.
C)
<strong>What product do you expect from the following reaction?  </strong> A)   B)   C)   D) Some of these would be formed. E) None of these would be formed.
D) Some of these would be formed.
E) None of these would be formed.
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28
Which would be the most acidic proton in the molecule below? <strong>Which would be the most acidic proton in the molecule below?  </strong> A) Protons a B) Proton b C) Proton c D) Protons d E) Protons e

A) Protons a
B) Proton b
C) Proton c
D) Protons d
E) Protons e
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29
What would be the expected product of the following reaction sequence? <strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)

A)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)
B)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)
C)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)
D)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)
E)
<strong>What would be the expected product of the following reaction sequence?  </strong> A)   B)   C)   D)   E)
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