EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
6th Edition
ISBN: 8220103151757
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 23, Problem 23.1P
Interpretation Introduction

(a)

Interpretation:

The structure of N-isopropylaniline is to be drawn.

Concept introduction:

Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are basic in nature because the nitrogen can donate its lone pairs and also the ability of the nitrogen to accept the proton in water.

Expert Solution
Check Mark

Answer to Problem 23.1P

The structure of N-isopropylaniline is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  1

Explanation of Solution

The name N-isopropylaniline indicates that it consists of the structure of aniline compound. One hydrogen atom of NH2 group of aniline is replaced by the isopropyl group as predicted by the structure of the given compound. The structure of N-isopropylaniline is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  2

Figure 1

Conclusion

The structure of N-isopropylaniline is shown in Figure 1.

Interpretation Introduction

(b)

Interpretation:

The structure of tert-butylamine is to be drawn.

Concept introduction:

Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are basic in nature because the nitrogen can donate its lone pairs and also the ability of the nitrogen to accept the proton in water.

Expert Solution
Check Mark

Answer to Problem 23.1P

The structure of tert-butylamine is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  3

Explanation of Solution

The name tert-butylamine indicates that it consist of tert-butyl group. The tert-butyl group is attached to an amine group. The structure of tert-butylamine is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  4

Figure 2

Conclusion

The structure of tert-butylamine is shown in Figure 2.

Interpretation Introduction

(c)

Interpretation:

The structure of 3-methoxypiperidine is to be drawn.

Concept introduction:

Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are basic in nature because the nitrogen can donate its lone pairs and also the ability of the nitrogen to accept the proton in water.

Expert Solution
Check Mark

Answer to Problem 23.1P

The structure of 3-methoxypiperidine is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  5

Explanation of Solution

The name 3-methoxypiperidine indicates that it contains a piperidine ring. The methoxy group is attached to the third carbon of the piperidine ring. The structure of 3-methoxypiperidine is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  6

Figure 3

Conclusion

The structure of 3-methoxypiperidine is shown in Figure 3.

Interpretation Introduction

(d)

Interpretation:

The structure of 2, 2-dimethyl-3-hexanamine is to be drawn.

Concept introduction:

Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are basic in nature because the nitrogen can donate its lone pairs and also the ability of the nitrogen to accept the proton in water.

Expert Solution
Check Mark

Answer to Problem 23.1P

The structure of 2, 2-dimethyl-3-hexanamine is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  7

Explanation of Solution

The name 2, 2-dimethyl-3-hexanamine indicates that it contains six number carbon chains. The amine group is attached to third carbon and two methyl groups are attached to the second carbon of the chain. The structure of 2, 2-dimethyl-3-hexanamine is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  8

Figure 4

Conclusion

The structure of 2, 2-dimethyl-3-hexanamine is shown in Figure 4.

Interpretation Introduction

(e)

Interpretation:

The structure of ethyl 2-(diethylamino)pentanoate is to be drawn.

Concept introduction:

Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are basic in nature because the nitrogen can donate its lone pairs and also the ability of the nitrogen to accept the proton in water.

Expert Solution
Check Mark

Answer to Problem 23.1P

The structure of ethyl 2-(diethylamino)pentanoate is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  9

Explanation of Solution

The name ethyl 2-(diethylamino)pentanoate indicates that it contains ethyl pentanoate as the parent structure. The diethyl amine group is attached to the second carbon of the ethyl pentanoate. The structure of ethyl 2-(diethylamino)pentanoate is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  10

Figure 5

Conclusion

The structure of ethyl 2-(diethylamino)pentanoate is shown in Figure 5.

Interpretation Introduction

(f)

Interpretation:

The structure of N,N-diethyl-3-heptanamine is to be drawn.

Concept introduction:

Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are basic in nature because the nitrogen can donate its lone pairs and also the ability of the nitrogen to accept the proton in water.

Expert Solution
Check Mark

Answer to Problem 23.1P

The structure of N,N-diethyl-3-heptanamine is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  11

Explanation of Solution

The name N,N-diethyl-3-heptanamine indicates that it contains seven number carbon chains. The diethyl amine group is attached to third carbon of the seven number carbon chains. The structure of N,N-diethyl-3-heptanamine is shown below.

EBK ORGANIC CHEMISTRY, Chapter 23, Problem 23.1P , additional homework tip  12

Figure 6

Conclusion

The structure of N,N-diethyl-3-heptanamine is shown in Figure 6.

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Chapter 23 Solutions

EBK ORGANIC CHEMISTRY

Ch. 23 - Prob. 23.11PCh. 23 - Prob. 23.12PCh. 23 - Prob. 23.13PCh. 23 - Prob. 23.14PCh. 23 - Prob. 23.15PCh. 23 - Prob. 23.16PCh. 23 - Prob. 23.17PCh. 23 - Prob. 23.18PCh. 23 - Prob. 23.19PCh. 23 - Prob. 23.20PCh. 23 - Prob. 23.21PCh. 23 - Prob. 23.22PCh. 23 - Prob. 23.23PCh. 23 - Prob. 23.24PCh. 23 - Prob. 23.25PCh. 23 - Prob. 23.26PCh. 23 - Prob. 23.27PCh. 23 - Prob. 23.28PCh. 23 - Prob. 23.29PCh. 23 - Prob. 23.30PCh. 23 - Prob. 23.31PCh. 23 - Prob. 23.32PCh. 23 - Prob. 23.33PCh. 23 - Prob. 23.34PCh. 23 - Prob. 23.35PCh. 23 - Prob. 23.36PCh. 23 - Prob. 23.37PCh. 23 - Prob. 23.38PCh. 23 - Prob. 23.39PCh. 23 - Prob. 23.40PCh. 23 - Prob. 23.41PCh. 23 - Prob. 23.42PCh. 23 - Prob. 23.43PCh. 23 - Prob. 23.44APCh. 23 - Prob. 23.45APCh. 23 - Prob. 23.46APCh. 23 - Prob. 23.47APCh. 23 - Prob. 23.48APCh. 23 - Prob. 23.49APCh. 23 - Prob. 23.50APCh. 23 - Prob. 23.51APCh. 23 - Prob. 23.52APCh. 23 - Prob. 23.53APCh. 23 - Prob. 23.54APCh. 23 - Prob. 23.55APCh. 23 - Prob. 23.56APCh. 23 - Prob. 23.57APCh. 23 - Prob. 23.58APCh. 23 - Prob. 23.59APCh. 23 - Prob. 23.60APCh. 23 - Prob. 23.61APCh. 23 - Prob. 23.62APCh. 23 - Prob. 23.63APCh. 23 - Prob. 23.64APCh. 23 - Prob. 23.65APCh. 23 - Prob. 23.66APCh. 23 - Prob. 23.67APCh. 23 - Prob. 23.68APCh. 23 - Prob. 23.69APCh. 23 - Prob. 23.70APCh. 23 - Prob. 23.71APCh. 23 - Prob. 23.72APCh. 23 - Prob. 23.73APCh. 23 - Prob. 23.74APCh. 23 - Prob. 23.75APCh. 23 - Prob. 23.76APCh. 23 - Prob. 23.77APCh. 23 - Prob. 23.78APCh. 23 - Prob. 23.79APCh. 23 - Prob. 23.80APCh. 23 - Prob. 23.81AP
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