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Time left 1:05:05 In the nitration of aniline, the first equilibrium is established quickly with majority of starting material as the ammonium salt, shown below. Why is the product not entirely m-nitroaniline? NH, NH, HNO, Approximately equal amounts of ortho-, meta- and para-nitro products H,SO, The rate of reaction of aniline is much faster than protonated aniline The ammonium group is a strong deactivator and directs meta. OThe amino group is a strong activator and directs meta The nitro group is a strong deactivator and directs meta. Steric effects limit the amount of ortho-nitro product Question 3 Not yet answered III

Time left 1:05:05 In the nitration of aniline, the first equilibrium is established quickly with majority of starting material as the ammonium salt, shown below. Why is the product not entirely m-nitroaniline? NH, NH, HNO, Approximately equal amounts of ortho-, meta- and para-nitro products H,SO, The rate of reaction of aniline is much faster than protonated aniline The ammonium group is a strong deactivator and directs meta. OThe amino group is a strong activator and directs meta The nitro group is a strong deactivator and directs meta. Steric effects limit the amount of ortho-nitro product Question 3 Not yet answered III

Organic Chemistry
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter24: Catalytic Carbon-carbon Bond Formation
Section: Chapter Questions
Problem 24.9P
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In the nitration of aniline, the first equilibrium is established quickly with majority of starting material as the ammonium salt, shown below. Why is the product not entirely m-nitroaniline?  The rate of reaction of aniline is much faster than protonated aniline The ammonium group is a strong deactivator and directs meta. The amino group is a strong activator and directs meta The nitro group is a strong deactivator and directs meta. Steric effects limit the amount of ortho-nitro
8:32 05 N Time left 1:05:05 In the nitration of aniline, the first equilibrium is established quickly with majority of starting material as the ammonium salt, shown below. Why is the product not entirely m-nitroaniline? NH, NH3 HNO3 Approximately equal amounts of ortho-, meta- and para-nitro products H,SO, The rate of reaction of aniline is much faster than protonated aniline The ammonium group is a strong deactivator and directs meta. OThe amino group is a strong activator and directs meta The nitro group is a strong deactivator and directs meta. Steric effects limit the amount of ortho-nitro product Question 3 Not yet answered Marked out of 2.00 P Flag question Choose the correct statement for the following sequence of reactions? (EAS = electrophilic aromatic substitution) II
Transcribed Image Text:8:32 05 N Time left 1:05:05 In the nitration of aniline, the first equilibrium is established quickly with majority of starting material as the ammonium salt, shown below. Why is the product not entirely m-nitroaniline? NH, NH3 HNO3 Approximately equal amounts of ortho-, meta- and para-nitro products H,SO, The rate of reaction of aniline is much faster than protonated aniline The ammonium group is a strong deactivator and directs meta. OThe amino group is a strong activator and directs meta The nitro group is a strong deactivator and directs meta. Steric effects limit the amount of ortho-nitro product Question 3 Not yet answered Marked out of 2.00 P Flag question Choose the correct statement for the following sequence of reactions? (EAS = electrophilic aromatic substitution) II
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