Organic Chemistry-Package(Custom)
Organic Chemistry-Package(Custom)
4th Edition
ISBN: 9781259141089
Author: SMITH
Publisher: MCG
Question
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Chapter 25, Problem 25.33P
Interpretation Introduction

(a)

Interpretation: The product formed in the given reaction is to be drawn.

Concept introduction: Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2,HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2,HCl. Aryl diazonium salts undergo substitution reaction and form different benzene derivatives.

Interpretation Introduction

(b)

Interpretation: The product formed in the given reaction is to be drawn.

Concept introduction: Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2,HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2,HCl. Aryl diazonium salts undergo substitution reaction and form different benzene derivatives.

Interpretation Introduction

(c)

Interpretation: The product formed in the given reaction is to be drawn.

Concept introduction: Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2,HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2,HCl. Aryl diazonium salts undergo substitution reaction and form different benzene derivatives.

Interpretation Introduction

(d)

Interpretation: The product formed in the given reaction is to be drawn.

Concept introduction: Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2,HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2,HCl. Aryl diazonium salts undergo substitution reaction and form different benzene derivatives.

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Chapter 25 Solutions

Organic Chemistry-Package(Custom)

Ch. 25 - Prob. 25.11PCh. 25 - Prob. 25.12PCh. 25 - Prob. 25.13PCh. 25 - Prob. 25.14PCh. 25 - Prob. 25.15PCh. 25 - Prob. 25.16PCh. 25 - Prob. 25.17PCh. 25 - Prob. 25.18PCh. 25 - Draw the products of each acidbase reaction....Ch. 25 - Prob. 25.20PCh. 25 - Prob. 25.21PCh. 25 - Prob. 25.22PCh. 25 - Prob. 25.23PCh. 25 - Problem 25.22 Which nitrogen atom in each compound...Ch. 25 - Which N atom in each drug is more basic? a. b. c.Ch. 25 - Prob. 25.26PCh. 25 - Prob. 25.27PCh. 25 - Prob. 25.28PCh. 25 - Prob. 25.29PCh. 25 - Prob. 25.30PCh. 25 - Problem 25.28 Draw the major product formed in...Ch. 25 - Prob. 25.32PCh. 25 - Prob. 25.33PCh. 25 - Problem 25.31 Devise a synthesis of each compound...Ch. 25 - Prob. 25.35PCh. 25 - Problem 25.33 What starting materials are needed...Ch. 25 - Problem 25.34 (a) What two components are needed...Ch. 25 - Prob. 25.38PCh. 25 - Prob. 25.39PCh. 25 - Prob. 25.40PCh. 25 - 25.37 Varenicline (trade name Chantix) is a drug...Ch. 25 - Prob. 25.42PCh. 25 - Prob. 25.43PCh. 25 - Prob. 25.44PCh. 25 - Prob. 25.45PCh. 25 - Prob. 25.46PCh. 25 - Prob. 25.47PCh. 25 - Prob. 25.48PCh. 25 - Decide which N atom in each molecule is most basic...Ch. 25 - 25.44 Rank the nitrogen atoms in each compound in...Ch. 25 - 25.45 Explain why nitroaniline is a stronger base...Ch. 25 - 25.46 Explain the observed difference in the...Ch. 25 - 25.47 Why is pyrrole more acidic than...Ch. 25 - How would you prepare 3-phenyl-1-propanamine...Ch. 25 - Prob. 25.55PCh. 25 - Prob. 25.56PCh. 25 - Prob. 25.57PCh. 25 - Prob. 25.58PCh. 25 - 25.51 How would you separate toluene , benzoic...Ch. 25 - 25.52 Draw the products formed when methylaniline ...Ch. 25 - Prob. 25.61PCh. 25 - Prob. 25.62PCh. 25 - Prob. 25.63PCh. 25 - Prob. 25.64PCh. 25 - Prob. 25.65PCh. 25 - Prob. 25.66PCh. 25 - Prob. 25.67PCh. 25 - Prob. 25.68PCh. 25 - 25.60 A chiral amine A having the configuration...Ch. 25 - 25.61 Draw a stepwise mechanism for each...Ch. 25 - 25.62 Draw a stepwise mechanism for the following...Ch. 25 - Prob. 25.72PCh. 25 - Tertiary (3) aromatic amines react with NaNO2 and...Ch. 25 - Prob. 25.74PCh. 25 - Devise a synthesis of each compound from benzene....Ch. 25 - Prob. 25.76PCh. 25 - Prob. 25.77PCh. 25 - Prob. 25.78PCh. 25 - Prob. 25.79PCh. 25 - Synthesize each compound from benzene. Use a...Ch. 25 - Prob. 25.81PCh. 25 - Devise a synthesis of each compound from benzene,...Ch. 25 - Prob. 25.83PCh. 25 - 25.72 Three isomeric compounds A, B, and C, all...Ch. 25 - 25.73 Treatment of compound D with LiAlH4 followed...Ch. 25 - Prob. 25.86PCh. 25 - 25.75 Rank the following compounds in order of...Ch. 25 - Prob. 25.88PCh. 25 - Prob. 25.89PCh. 25 - Prob. 25.90P
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