Synthesis of 3-nitrophenol has to be proposed using 3-nitroaniline as starting material. Concept Introduction: Conversion of aromatic amines to phenol: Aromatic amines converted to arenediazonium salt by reacting with N a N O 2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

Question

These are in the wrong boxes. Why does the one on the left have a lower molar mass than the one on the right?

Answer 1

Question

Chapter 23.8, Problem 23.13P

(a)

Interpretation Introduction

Interpretation:

Synthesis of 3-nitrophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

(b)

Interpretation Introduction

Interpretation:

Synthesis of 3-bromo nitrobenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

(c)

Interpretation Introduction

Interpretation:

Synthesis of 1,3-dihydroxybenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

(d)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluoroaniline has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

(e)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluorophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

(f)

Interpretation Introduction

Interpretation:

Synthesis of 3-hydroxybenzonitrile has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

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These are in the wrong boxes. Why does the one on the left have a lower molar mass than the one on the right?

SYNTHESIS REACTIONS. For the following reactions, synthesize the given products from the given reactants. Multiple reactions/steps will be needed. For the one of the steps (ie reactions) in each synthesis, write out the mechanism for that reaction and draw an energy diagram showing the correct number of hills and valleys for that step's mechanism. CI b. a. Use acetylene (ethyne) and any alkyl halide as your starting materials Br C. d. "OH OH III. OH

Calculate the pH and the pOH of each of the following solutions at 25 °C for which the substances ionize completely: (a) 0.200 M HCl

Answer 2

Question

Chapter 23.8, Problem 23.13P

(a)

Interpretation Introduction

Interpretation:

Synthesis of 3-nitrophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

(b)

Interpretation Introduction

Interpretation:

Synthesis of 3-bromo nitrobenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

(c)

Interpretation Introduction

Interpretation:

Synthesis of 1,3-dihydroxybenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

(d)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluoroaniline has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

(e)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluorophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

(f)

Interpretation Introduction

Interpretation:

Synthesis of 3-hydroxybenzonitrile has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

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Answer 3

Question

Chapter 23.8, Problem 23.13P

(a)

Interpretation Introduction

Interpretation:

Synthesis of 3-nitrophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

(b)

Interpretation Introduction

Interpretation:

Synthesis of 3-bromo nitrobenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

(c)

Interpretation Introduction

Interpretation:

Synthesis of 1,3-dihydroxybenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

(d)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluoroaniline has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

(e)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluorophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

(f)

Interpretation Introduction

Interpretation:

Synthesis of 3-hydroxybenzonitrile has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

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Answer 4

Question

Chapter 23.8, Problem 23.13P

(a)

Interpretation Introduction

Interpretation:

Synthesis of 3-nitrophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

(b)

Interpretation Introduction

Interpretation:

Synthesis of 3-bromo nitrobenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

(c)

Interpretation Introduction

Interpretation:

Synthesis of 1,3-dihydroxybenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

(d)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluoroaniline has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

(e)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluorophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

(f)

Interpretation Introduction

Interpretation:

Synthesis of 3-hydroxybenzonitrile has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

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Answer 5

Chapter 23.8, Problem 23.13P

(a)

Interpretation Introduction

Interpretation:

Synthesis of 3-nitrophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

(b)

Interpretation Introduction

Interpretation:

Synthesis of 3-bromo nitrobenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

(c)

Interpretation Introduction

Interpretation:

Synthesis of 1,3-dihydroxybenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

(d)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluoroaniline has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

(e)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluorophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

(f)

Interpretation Introduction

Interpretation:

Synthesis of 3-hydroxybenzonitrile has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

Answer 6

Chapter 23.8, Problem 23.13P

(a)

Interpretation Introduction

Interpretation:

Synthesis of 3-nitrophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

Answer 7

Chapter 23.8, Problem 23.13P

(a)

Interpretation Introduction

Interpretation:

Synthesis of 3-nitrophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

Answer 8

(b)

Interpretation Introduction

Interpretation:

Synthesis of 3-bromo nitrobenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

Answer 9

(b)

Interpretation Introduction

Interpretation:

Synthesis of 3-bromo nitrobenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

Answer 10

(c)

Interpretation Introduction

Interpretation:

Synthesis of 1,3-dihydroxybenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

Answer 11

(c)

Interpretation Introduction

Interpretation:

Synthesis of 1,3-dihydroxybenzene has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

Answer 12

(d)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluoroaniline has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

Answer 13

(d)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluoroaniline has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

Answer 14

(e)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluorophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

Answer 15

(e)

Interpretation Introduction

Interpretation:

Synthesis of 3-fluorophenol has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Conversion of aromatic amines to phenol:

Aromatic amines converted to arenediazonium salt by reacting with NaNO2 in presence of aqueous sulfuric acid which further on heating with water forms a phenol.

Schiemann reaction: It is a method used to introduce fluorine into an aromatic ring. The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl followed by the reaction with NaBF4 or HBF4 that results in the introduction of a fluorine atom in the compound.

Answer 16

(f)

Interpretation Introduction

Interpretation:

Synthesis of 3-hydroxybenzonitrile has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

Answer 17

(f)

Interpretation Introduction

Interpretation:

Synthesis of 3-hydroxybenzonitrile has to be proposed using 3-nitroaniline as starting material.

Concept Introduction:

Hydrogenation:

Hydrogenation means the addition of hydrogen molecules to the unsaturated compound which makes them saturated hydrocarbon in the presence of catalyst.

Reaction of a primary aromatic amine with sodium nitrite:

The reaction of a primary aromatic amine with sodium nitrite in presence of aqueous HCl gives an arenediazonium salt.

Sandmeyer reaction: It reaction type of organic reaction where the diazonium group in an arenediazonium salt gets replaced by −Cl, −Br or −CN groups on reacting with HCl/CuCl, HBr/CuBr or HCN/CuCN.

Answer 18

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Ch. 23.1 - Prob. 23.1P Ch. 23.2 - Prob. 23.2P Ch. 23.2 - Prob. 23.3P Ch. 23.2 - Prob. 23.4P Ch. 23.5 - Prob. 23.5P Ch. 23.5 - Prob. AQ Ch. 23.5 - What is the hybridization of the nitrogen in...Ch. 23.5 - Prob. CQ Ch. 23.5 - The pKas of the conjugate acids of aniline and...Ch. 23.5 - Prob. EQ

Chapter 23 Solutions