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) I and II
D) None of the choices
Correct Answer
verified
Multiple Choice
A) a-Carbon
B) b-Carbon
C) Carbonyl carbon
D) Carbonyl carbon and b-carbon
Correct Answer
verified
Multiple Choice
A) Michael reaction
B) Aldol self-condensation
C) Dieckmann condensation
D) Robinson annulation
Correct Answer
verified
Multiple Choice
A) Multiple Claisen reaction
B) Differential Claisen reaction
C) Crossed Claisen reaction
D) Versatile Claisen reaction
Correct Answer
verified
Multiple Choice
A) Michael donor
B) Michael enolate
C) Michael nucleophile
D) Michael acceptor
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
Multiple Choice
A) an a,b-Unsaturated carbonyl compound and an enolate
B) a b-Ketoester and an enolate
C) a 1,5-Dicarbonyl compound and an enolate
D) a 1,3-Dicarbonyl compound and an enolate
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) 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) 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) Nucleophilic substitution
B) Electrophilic substitution
C) Electrophilic addition
D) Nucleophilic addition
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) b-Keto ester
B) a,b-Dicarbonyl compound
C) g-Dicarbonyl compound
D) b-Dicarbonyl compound
Correct Answer
verified
Multiple Choice
A) All esters can undergo Claisen reactions.
B) Only esters with two hydrogen atoms on the acarbon can undergo Claisen reactions.
C) Only esters with three hydrogen atoms on the acarbon can undergo Claisen reactions.
D) Only esters with two or three hydrogen atoms on the acarbon can undergo Claisen reactions.
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) Both I and II
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
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