Organic Chemistry Study Guide and Solutions
Organic Chemistry Study Guide and Solutions
6th Edition
ISBN: 9781936221868
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
Question
Book Icon
Chapter 16, Problem 16.64AP
Interpretation Introduction

Interpretation:

The reason as to why anisole protonates on oxygen in concentrated H2SO4 while 1, 3, 5-trimethoxybenzene protonates on the carbon of the ring is to be stated. Also, the structure of each conjugate acid is to be drawn.

Concept introduction:

Electron donating groups substituted on the aromatic ring are those which donates electron to the aromatic ring. Electron donating groups are ortho and para-directing. Electron withdrawing groups substituted on the aromatic ring are those which withdraw the electrons of the aromatic ring towards themselves and are meta-directing.

Blurred answer
Students have asked these similar questions
Complete the following proposed acid–base reactions, and predict whether the reactants or products are favored.
Show how acid derivatives hydrolyze to carboxylic acids under either acidic or basicconditions. Explain why some acid derivatives (amides, for example) require muchstronger conditions for hydrolysis than other derivatives.
The pKa of our product is ~ 2-3 units lower than the pKa of phenol. Draw all possible resonance structures of the conjugate base of the product, and use these to explain why our product is so much more acidic than phenol.

Chapter 16 Solutions

Organic Chemistry Study Guide and Solutions

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