ORGANIC CHEMISTRY-PACKAGE >CUSTOM<
ORGANIC CHEMISTRY-PACKAGE >CUSTOM<
10th Edition
ISBN: 9781260028355
Author: Carey
Publisher: MCG CUSTOM
Question
Book Icon
Chapter 13.15, Problem 20P
Interpretation Introduction

Interpretation:

The reaction mechanism for a reaction between 4-chloro-N-methylaniline and bromine is to be written.

Concept Introduction:

Amines are very strongly activating groups because the lone pair of nitrogen can delocalize on the ring and they are ortho/para directing.

Chlorine atom in electrophilic aromatic substitution act as weakly deactivating and it is ortho/para directing.

Blurred answer
Students have asked these similar questions
Please help with this graph.
ogin - PaymentN MapQuest 3 Overview - SAP NetW... Draw the major product of this reaction. Ignore inorganic byproducts. CI 1. NaBH4 2. H₂O C Clever | Portal Job Op Problem Atoms, Bonds and Rings Draw or tap a new bond to
2. Draw the remaining two resonance structures for the carbocation intermediate in the meta nitration of methyl benzoate AND explain why the meta orientation is preferred. Hint: how is the placement of the cation favorable after addition of nitronium relative to the electron withdrawing group? (2 pts) H NO2 CO₂Me

Chapter 13 Solutions

ORGANIC CHEMISTRY-PACKAGE >CUSTOM<

Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning