D1A Which reaction will NOT produce a compound with the carbon from the carbonyl group in the same oxidation state as in the starting material? OA cyclobutanone and water under basic catalysis OB. bicyclo[2.2.1]heptane-2-one with ethanol and an acid catalyst OCacetophenone and hydrazine at a pH =7 OD. cyclopentanone and hydrazine with KOH

Organic Chemistry
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Author:John E. McMurry
Publisher:John E. McMurry
Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution
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Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...
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QUESTION 57
D1A Which reaction will NOT produce a compound with the carbon from the carbonyl group in the same
oxidation state as in the starting material?
OA.
cyclobutanone and water under basic catalysis
OB.
bicyclo[2.2.1]heptane-2-one with ethanol and an acid catalyst
acetophenone and hydrazine at a pH = 7
OD.
cyclopentanone and hydrazine with KOH
QUESTION 58
B8E Which reaction will NOT form an enolate intermediate?
cyclohex-2-enone with butylmagnesium bromide
cyclohex-2-enone with lithium dimethylcuprate
cyclohex-2-enone with lithium di-isopropylamide
treatment of hexa-1,5-dien-3-ol with KH followed by Cope Rearrangement
QUESTION 50
Transcribed Image Text:QUESTION 57 D1A Which reaction will NOT produce a compound with the carbon from the carbonyl group in the same oxidation state as in the starting material? OA. cyclobutanone and water under basic catalysis OB. bicyclo[2.2.1]heptane-2-one with ethanol and an acid catalyst acetophenone and hydrazine at a pH = 7 OD. cyclopentanone and hydrazine with KOH QUESTION 58 B8E Which reaction will NOT form an enolate intermediate? cyclohex-2-enone with butylmagnesium bromide cyclohex-2-enone with lithium dimethylcuprate cyclohex-2-enone with lithium di-isopropylamide treatment of hexa-1,5-dien-3-ol with KH followed by Cope Rearrangement QUESTION 50
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