Chemistry For Today: General, Organic, And Biochemistry, Loose-leaf Version
Chemistry For Today: General, Organic, And Biochemistry, Loose-leaf Version
9th Edition
ISBN: 9781305968707
Author: Spencer L. Seager
Publisher: Brooks Cole
Question
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Chapter 16, Problem 16.14E
Interpretation Introduction

(a)

Interpretation:

The structural formula for 3ethyl2pentanamine is to be stated.

Concept introduction:

Amines are given common names by listing the alkyl groups attached to nitrogen atom in alphabetical order followed by the suffix –amine. The prefixes di and tri are used when there are more than one identical groups present. According to IUPAC rules, the longest chain is determined and the ending of the alkane is changed from –e to –amine. The position of the amino group is indicated by a number and the prefix N is used if the substituents are attached to nitrogen atom.

Interpretation Introduction

(b)

Interpretation:

The structural formula for methylaniline is to be stated.

Concept introduction:

Amines are given common names by listing the alkyl groups attached to nitrogen atom in alphabetical order followed by the suffix –amine. The prefixes di and tri are used when there are more than one identical groups present. According to IUPAC rules, the longest chain is determined and the ending of the alkane is changed from –e to –amine. The position of the amino group is indicated by a number and the prefix N is used if the substituents are attached to nitrogen atom.

Interpretation Introduction

(c)

Interpretation:

The structural formula for N,Ndiphenylaniline is to be stated.

Concept introduction:

Amines are given common names by listing the alkyl groups attached to nitrogen atom in alphabetical order followed by the suffix –amine. The prefixes di and tri are used when there are more than one identical groups present. According to IUPAC rules, the longest chain is determined and the ending of the alkane is changed from –e to –amine. The position of the amino group is indicated by a number and the prefix N is used if the substituents are attached to nitrogen atom.

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Chapter 16 Solutions

Chemistry For Today: General, Organic, And Biochemistry, Loose-leaf Version

Ch. 16 - Prob. 16.11ECh. 16 - Prob. 16.12ECh. 16 - Prob. 16.13ECh. 16 - Prob. 16.14ECh. 16 - Prob. 16.15ECh. 16 - Prob. 16.16ECh. 16 - Prob. 16.17ECh. 16 - Prob. 16.18ECh. 16 - Prob. 16.19ECh. 16 - Draw diagrams similar to Figure 16.1 to illustrate...Ch. 16 - Prob. 16.21ECh. 16 - Prob. 16.22ECh. 16 - Prob. 16.23ECh. 16 - Prob. 16.24ECh. 16 - Prob. 16.25ECh. 16 - Prob. 16.26ECh. 16 - Prob. 16.27ECh. 16 - Prob. 16.28ECh. 16 - Prob. 16.29ECh. 16 - Prob. 16.30ECh. 16 - Prob. 16.31ECh. 16 - Prob. 16.32ECh. 16 - Prob. 16.33ECh. 16 - Describe the general structure of a neuron.Ch. 16 - Name the two amino acids that are starting...Ch. 16 - Prob. 16.36ECh. 16 - Prob. 16.37ECh. 16 - Prob. 16.38ECh. 16 - Prob. 16.39ECh. 16 - Prob. 16.40ECh. 16 - Prob. 16.41ECh. 16 - Prob. 16.42ECh. 16 - Why are alkaloids weakly basic?Ch. 16 - Prob. 16.44ECh. 16 - Prob. 16.45ECh. 16 - Prob. 16.46ECh. 16 - Prob. 16.47ECh. 16 - Prob. 16.48ECh. 16 - Prob. 16.49ECh. 16 - Prob. 16.50ECh. 16 - Prob. 16.51ECh. 16 - Complete the following reactions: a. b.Ch. 16 - Complete the following reactions: a. b.Ch. 16 - Prob. 16.54ECh. 16 - What are the products of the acid hydrolysis of...Ch. 16 - Prob. 16.56ECh. 16 - Prob. 16.57ECh. 16 - Prob. 16.58ECh. 16 - Prob. 16.59ECh. 16 - Prob. 16.60ECh. 16 - Prob. 16.61ECh. 16 - Prob. 16.62ECh. 16 - Prob. 16.63ECh. 16 - Prob. 16.64ECh. 16 - Prob. 16.65ECh. 16 - Prob. 16.66ECh. 16 - Prob. 16.67ECh. 16 - Prob. 16.68ECh. 16 - Prob. 16.69ECh. 16 - Prob. 16.70ECh. 16 - Prob. 16.71ECh. 16 - The stimulant in coffee is: a. tannic acid b....Ch. 16 - What are the most likely products of a reaction...
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