a) Interpretation: Whether N,N-dimethylamino group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated. Concept introduction: In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect. Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating. To state: Whether N,N-dimethylamino group is an activator or deactivator and whether it is a, o-, p-director or m-director.

Question

+ C8H16O2 (Fatty acid) + 11 02 → 8 CO2 a. Which of the above are the reactants? b. Which of the above are the products? H2o CO₂ c. Which reactant is the electron donor? Futty acid d. Which reactant is the electron acceptor? e. Which of the product is now reduced? f. Which of the products is now oxidized? 02 #20 102 8 H₂O g. Where was the carbon initially in this chemical reaction and where is it now that it is finished? 2 h. Where were the electrons initially in this chemical reaction and where is it now that it is finished?

Answer 1

Question

Chapter 16.SE, Problem 46AP

Interpretation Introduction

a)

Interpretation:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a, o-, p-director or m-director.

Interpretation Introduction

b)

Interpretation:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director.

Interpretation Introduction

c)

Interpretation:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director.

Interpretation Introduction

d)

Interpretation:

Whether the carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director.

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+ C8H16O2 (Fatty acid) + 11 02 → 8 CO2 a. Which of the above are the reactants? b. Which of the above are the products? H2o CO₂ c. Which reactant is the electron donor? Futty acid d. Which reactant is the electron acceptor? e. Which of the product is now reduced? f. Which of the products is now oxidized? 02 #20 102 8 H₂O g. Where was the carbon initially in this chemical reaction and where is it now that it is finished? 2 h. Where were the electrons initially in this chemical reaction and where is it now that it is finished?

→ Acetyl-CoA + 3NAD+ + 1FAD + 1ADP 2CO2 + CoA + 3NADH + 1FADH2 + 1ATP a. Which of the above are the reactants? b. Which of the above are the products? c. Which reactant is the electron donor? d. Which reactants are the electron acceptors? e. Which of the products are now reduced? f. Which product is now oxidized? g. Which process was used to produce the ATP? h. Where was the energy initially in this chemical reaction and where is it now that it is finished? i. Where was the carbon initially in this chemical reaction and where is it now that it is finished? j. Where were the electrons initially in this chemical reaction and where is it now that it is finished?

Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. OCH 3 (Choose one) OH (Choose one) Br (Choose one) Explanation Check NO2 (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | A

Answer 2

Question

Chapter 16.SE, Problem 46AP

Interpretation Introduction

a)

Interpretation:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a, o-, p-director or m-director.

Interpretation Introduction

b)

Interpretation:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director.

Interpretation Introduction

c)

Interpretation:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director.

Interpretation Introduction

d)

Interpretation:

Whether the carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director.

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Answer 3

Question

Chapter 16.SE, Problem 46AP

Interpretation Introduction

a)

Interpretation:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a, o-, p-director or m-director.

Interpretation Introduction

b)

Interpretation:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director.

Interpretation Introduction

c)

Interpretation:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director.

Interpretation Introduction

d)

Interpretation:

Whether the carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director.

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Answer 4

Question

Chapter 16.SE, Problem 46AP

Interpretation Introduction

a)

Interpretation:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a, o-, p-director or m-director.

Interpretation Introduction

b)

Interpretation:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director.

Interpretation Introduction

c)

Interpretation:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director.

Interpretation Introduction

d)

Interpretation:

Whether the carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director.

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Answer 5

Chapter 16.SE, Problem 46AP

Interpretation Introduction

a)

Interpretation:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a, o-, p-director or m-director.

Interpretation Introduction

b)

Interpretation:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director.

Interpretation Introduction

c)

Interpretation:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director.

Interpretation Introduction

d)

Interpretation:

Whether the carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director.

Answer 6

Chapter 16.SE, Problem 46AP

Interpretation Introduction

a)

Interpretation:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a, o-, p-director or m-director.

Answer 7

Chapter 16.SE, Problem 46AP

Interpretation Introduction

a)

Interpretation:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether N,N-dimethylamino group is an activator or deactivator and whether it is a, o-, p-director or m-director.

Answer 8

Interpretation Introduction

b)

Interpretation:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director.

Answer 9

Interpretation Introduction

b)

Interpretation:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether cyclopentyl group is an activator or deactivator and whether it is an o-, p-director or m-director.

Answer 10

Interpretation Introduction

c)

Interpretation:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director.

Answer 11

Interpretation Introduction

c)

Interpretation:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether ethoxy group is an activator or deactivator and whether it is an o-, p-director or m-director.

Answer 12

Interpretation Introduction

d)

Interpretation:

Whether the carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director.

Answer 13

Interpretation Introduction

d)

Interpretation:

Whether the carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director is to be stated.

Concept introduction:

In aromatic substitution reactions the activating or deactivating and orienting effects of a substituent attached to the benzene ring can be decided from its resonance and inductive effects. The orientation is decided by the resonance effect while the activating or deactivating effect is decided both by resonance and inductive effects. Both effects may reinforce or oppose each other. However the resonance effect is much stronger than the inductive effect.

Electron releasing groups, except halogens, normally are activators and ortho & para directors. Electron withdrawing groups normally are deactivators and meta directors. Halogens are ortho & para directing but are deactivating.

To state:

Whether carbonyl group is an activator or deactivator and whether it is a o-, p-director or m-director.

Answer 14

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Ch. 16.1 - Prob. 1P Ch. 16.2 - Propose a mechanism for the electrophilic...Ch. 16.2 - How many products might be formed on chlorination...Ch. 16.2 - When benzene is treated with D2SÅª4. deuterium...Ch. 16.3 - Prob. 5P Ch. 16.3 - What is the major monosubstitution product from...Ch. 16.3 - Identify the carboxylic acid chloride that might...Ch. 16.4 - Rank the compounds in each of the following groups...Ch. 16.4 - Predict the major products of the following...Ch. 16.4 - Prob. 10P

Chapter 16 Solutions