The reaction of N-chloro aniline with alpha-(methylsulfanyl) ketones O Replacement of a nucleophile Electrophilic replacement Add a nickel add electrophile O Q14 * 2-azabicyclo[2.2.2]oct-2-ene O 1-azabicyclo[2.2.2]oct-2-ene 1-azabicyclo[2.4,2]oct-2-ene Q15* O 6-thiaspiro[4.5]decane O 1-thiaspiro[4.5]decane O2-thiaspiro[4.5]decane O All answers are wrong
The reaction of N-chloro aniline with alpha-(methylsulfanyl) ketones O Replacement of a nucleophile Electrophilic replacement Add a nickel add electrophile O Q14 * 2-azabicyclo[2.2.2]oct-2-ene O 1-azabicyclo[2.2.2]oct-2-ene 1-azabicyclo[2.4,2]oct-2-ene Q15* O 6-thiaspiro[4.5]decane O 1-thiaspiro[4.5]decane O2-thiaspiro[4.5]decane O All answers are wrong
Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution
Section16.SE: Something Extra
Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...
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![The reaction of N-chloro aniline with alpha-(methylsulfanyl) ketones
Replacement of a nucleophile
Electrophilic replacement
Add a nickel
add electrophile
ΟΟΟ
O
Q14 *
ΟΟΟ
2-azabicyclo[2.2.2]oct-2-ene
1-azabicyclo[2.2.2]oct-2-ene
O 1-azabicyclo[2.4,2]oct-2-ene
Q15*
6-thiaspiro[4.5]decane
O 1-thiaspiro[4.5]decane
2-thiaspiro[4.5]decane
O All answers are wrong
O O O O](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa065638e-41ee-4b27-900e-c60d238f25fc%2Fa18de81b-dee8-4da3-97b0-b8630bbae0b1%2F248r9mh_processed.jpeg&w=3840&q=75)
Transcribed Image Text:The reaction of N-chloro aniline with alpha-(methylsulfanyl) ketones
Replacement of a nucleophile
Electrophilic replacement
Add a nickel
add electrophile
ΟΟΟ
O
Q14 *
ΟΟΟ
2-azabicyclo[2.2.2]oct-2-ene
1-azabicyclo[2.2.2]oct-2-ene
O 1-azabicyclo[2.4,2]oct-2-ene
Q15*
6-thiaspiro[4.5]decane
O 1-thiaspiro[4.5]decane
2-thiaspiro[4.5]decane
O All answers are wrong
O O O O
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