A) I
B) II
C) I and II
D) None of the choices
Correct Answer
verified
Multiple Choice
A) Enolate formation,elimination,nucleophilic addition
B) Enolate formation,nucleophilic addition,elimination
C) Elimination,enolate formation,nucleophilic addition
D) Nucleophilic addition,enolate formation,elimination
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) Multiple Aldol reaction
B) Crossed Aldol reaction
C) Differential Aldol reaction
D) Versatile Aldol reaction
Correct Answer
verified
Multiple Choice
A) The electrophilic carbonyl component is relatively unhindered and is used in excess.
B) The electrophilic carbonyl carbon component is relatively hindered and is used in limited amount.
C) The nucleophilic carbonyl component is relatively unhindered and is used in excess.
D) The nucleophilic carbonyl component is relatively hindered and is used in limited amount.
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) the Aldol reaction involves substitution while the Claisen reaction involves addition.
B) the Aldol reaction is acid catalyzed while the Claisen reaction is base-catalyzed.
C) the Aldol reaction is base catalyzed while the Claisen reaction requires a full equivalent of base.
D) the Aldol reaction is base catalyzed while the Claisen reaction is acid-catalyzed.
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) I
B) II
C) I and II
D) None of the choices
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) b-Hydroxy ester
B) b-Keto ester
C) a-Keto ester
D) g-Hydroxy ester
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) NaOCH3 is a stronger base than NaOCH2CH3,and this reaction requires a stronger base.
B) NaOCH3 is a weaker base than NaOCH2CH3,and this reaction requires a weaker base.
C) Transesterfication can occur when esters react,and this transesterfication would result in a mixture of products.
D) NaOCH3 is more soluble than NaOCH2CH3 in organic solvents,and this reaction requires a full equivalent of base to proceed.A full equivalent of NaOCH2CH3 would not dissolve,so the reaction would not proceed.
Correct Answer
verified
Multiple Choice
A) a-Hydroxy carbonyl compound
B) b-Hydroxy carbonyl compound
C) g-Hydroxy carbonyl compound
D) a,b-Hydroxy carbonyl compound
Correct Answer
verified
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