Living By Chemistry: First Edition Textbook
Living By Chemistry: First Edition Textbook
1st Edition
ISBN: 9781559539418
Author: Angelica Stacy
Publisher: MAC HIGHER
Question
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Chapter U2.20, Problem 9E

(a)

Interpretation Introduction

Interpretation: The molecular formulas for citronellol and geraniol needs to be determined.

Concept Introduction: Chemical compounds with same molecular formula having different structure are known as isomers. Isomers having same number of atoms of each type but bonded together in a different sequence (spatial arrangement) are known as stereoisomers.

There are two kinds of stereo isomers- Geometrical and optical.

(a)

Expert Solution
Check Mark

Explanation of Solution

The given structures are as follows:

Living By Chemistry: First Edition Textbook, Chapter U2.20, Problem 9E , additional homework tip  1

From the above structures, molecular formula of the compounds can be determined as follows:

C10H21O −Citronellol

C10H18O- Gerniol

(b)

Interpretation Introduction

Interpretation: The two distinct smells of the molecule citronellol needs to be explained.

Concept Introduction: Chemical compounds with same molecular formula having different structure are known as isomers. Isomers having same number of atoms of each type but bonded together in a different sequence (spatial arrangement) are known as stereoisomers.

There are two kinds of stereo isomers- Geometrical and optical.

(b)

Expert Solution
Check Mark

Explanation of Solution

The formula of citronellol is C10H21O. The structure is represented as follows:

Living By Chemistry: First Edition Textbook, Chapter U2.20, Problem 9E , additional homework tip  2

There are two optical isomers which are non-superimposable mirror image of each other.

Living By Chemistry: First Edition Textbook, Chapter U2.20, Problem 9E , additional homework tip  3Living By Chemistry: First Edition Textbook, Chapter U2.20, Problem 9E , additional homework tip  4

Isomer of Citronellol

Thus, the two different smells are due to two different optical isomers of citronellol.

(c)

Interpretation Introduction

Interpretation: The reason for only one smell of geraniol smell needs to be explained.

Concept Introduction: Chemical compounds with same molecular formula having different structure are known as isomers. Isomers having same number of atoms of each type but bonded together in a different sequence (spatial arrangement) are known as stereoisomers.

There are two kinds of stereo isomers- Geometrical and optical.

(c)

Expert Solution
Check Mark

Explanation of Solution

The molecular formula of geraniol is C10H18O. The structure is represented as follows:

Living By Chemistry: First Edition Textbook, Chapter U2.20, Problem 9E , additional homework tip  5

Geraniol

It can show geometrical isomerism. The E-isomer and Z-isomer are as follows:

Living By Chemistry: First Edition Textbook, Chapter U2.20, Problem 9E , additional homework tip  6Living By Chemistry: First Edition Textbook, Chapter U2.20, Problem 9E , additional homework tip  7

Trans-Form Cis-Form

Due to absence of optical isomerism, there is only one smell of the molecule.

Chapter U2 Solutions

Living By Chemistry: First Edition Textbook

Ch. U2.2 - Prob. 3ECh. U2.2 - Prob. 4ECh. U2.2 - Prob. 5ECh. U2.2 - Prob. 6ECh. U2.2 - Prob. 7ECh. U2.3 - Prob. 1TAICh. U2.3 - Prob. 1ECh. U2.3 - Prob. 2ECh. U2.3 - Prob. 3ECh. U2.3 - Prob. 4ECh. U2.3 - Prob. 5ECh. U2.4 - Prob. 1TAICh. U2.4 - Prob. 1ECh. U2.4 - Prob. 2ECh. U2.4 - Prob. 3ECh. U2.4 - Prob. 4ECh. U2.4 - Prob. 5ECh. U2.4 - Prob. 6ECh. U2.4 - Prob. 7ECh. U2.4 - Prob. 8ECh. U2.5 - Prob. 1TAICh. U2.5 - Prob. 1ECh. U2.5 - Prob. 2ECh. U2.5 - Prob. 3ECh. U2.5 - Prob. 4ECh. U2.5 - Prob. 5ECh. U2.5 - Prob. 6ECh. U2.5 - Prob. 7ECh. U2.5 - Prob. 8ECh. U2.5 - Prob. 9ECh. U2.6 - Prob. 1TAICh. U2.6 - Prob. 1ECh. U2.6 - Prob. 2ECh. U2.6 - Prob. 3ECh. U2.6 - Prob. 4ECh. U2.6 - Prob. 5ECh. U2.6 - Prob. 6ECh. U2.6 - Prob. 7ECh. U2.6 - Prob. 8ECh. U2.6 - Prob. 9ECh. U2.6 - Prob. 10ECh. U2.6 - Prob. 11ECh. U2.7 - Prob. 1TAICh. U2.7 - Prob. 1ECh. U2.7 - Prob. 2ECh. U2.7 - Prob. 3ECh. U2.7 - Prob. 4ECh. U2.7 - Prob. 5ECh. U2.8 - Prob. 1TAICh. U2.8 - Prob. 1ECh. U2.8 - Prob. 2ECh. U2.8 - Prob. 3ECh. U2.8 - Prob. 4ECh. U2.8 - Prob. 5ECh. U2.8 - Prob. 6ECh. U2.9 - Prob. 1TAICh. U2.9 - Prob. 1ECh. U2.9 - Prob. 2ECh. U2.9 - Prob. 3ECh. U2.9 - Prob. 4ECh. U2.9 - Prob. 5ECh. U2.9 - Prob. 6ECh. U2.9 - Prob. 7ECh. U2.10 - Prob. 1TAICh. U2.10 - Prob. 1ECh. U2.10 - Prob. 2ECh. U2.10 - Prob. 3ECh. U2.10 - Prob. 4ECh. U2.10 - Prob. 5ECh. U2.10 - Prob. 6ECh. U2.10 - Prob. 7ECh. U2.10 - Prob. 8ECh. U2.10 - Prob. 9ECh. U2.11 - Prob. 1TAICh. U2.11 - Prob. 1ECh. U2.11 - Prob. 2ECh. U2.11 - Prob. 3ECh. U2.11 - Prob. 4ECh. U2.11 - Prob. 5ECh. U2.11 - Prob. 6ECh. U2.11 - Prob. 7ECh. U2.12 - Prob. 1TAICh. U2.12 - Prob. 1ECh. U2.12 - Prob. 2ECh. U2.12 - Prob. 3ECh. U2.12 - Prob. 4ECh. U2.12 - Prob. 5ECh. U2.12 - Prob. 6ECh. U2.12 - Prob. 7ECh. U2.13 - Prob. 1TAICh. U2.13 - Prob. 1ECh. U2.13 - Prob. 2ECh. U2.13 - Prob. 3ECh. U2.13 - Prob. 4ECh. U2.13 - Prob. 5ECh. U2.14 - Prob. 1TAICh. U2.14 - Prob. 1ECh. U2.14 - Prob. 2ECh. U2.14 - Prob. 3ECh. U2.14 - Prob. 4ECh. U2.14 - Prob. 5ECh. U2.14 - Prob. 6ECh. U2.14 - Prob. 7ECh. U2.14 - Prob. 8ECh. U2.15 - Prob. 1TAICh. U2.15 - Prob. 1ECh. U2.15 - Prob. 2ECh. U2.15 - Prob. 4ECh. U2.15 - Prob. 5ECh. U2.15 - Prob. 6ECh. U2.16 - Prob. 1TAICh. U2.16 - Prob. 1ECh. U2.16 - Prob. 2ECh. U2.16 - Prob. 3ECh. U2.16 - Prob. 4ECh. U2.16 - Prob. 6ECh. U2.16 - Prob. 7ECh. U2.17 - Prob. 1TAICh. U2.17 - Prob. 1ECh. U2.17 - Prob. 2ECh. U2.17 - Prob. 3ECh. U2.17 - Prob. 4ECh. U2.17 - Prob. 5ECh. U2.17 - Prob. 6ECh. U2.17 - Prob. 7ECh. U2.17 - Prob. 8ECh. U2.17 - Prob. 9ECh. U2.18 - Prob. 1TAICh. U2.18 - Prob. 1ECh. U2.18 - Prob. 2ECh. U2.18 - Prob. 3ECh. U2.18 - Prob. 4ECh. U2.18 - Prob. 5ECh. U2.18 - Prob. 6ECh. U2.18 - Prob. 7ECh. U2.19 - Prob. 1TAICh. U2.19 - Prob. 1ECh. U2.19 - Prob. 2ECh. U2.19 - Prob. 3ECh. U2.19 - Prob. 4ECh. U2.19 - Prob. 5ECh. U2.19 - Prob. 6ECh. U2.19 - Prob. 7ECh. U2.19 - Prob. 8ECh. U2.19 - Prob. 9ECh. U2.20 - Prob. 1TAICh. U2.20 - Prob. 1ECh. U2.20 - Prob. 2ECh. U2.20 - Prob. 3ECh. U2.20 - Prob. 4ECh. U2.20 - Prob. 5ECh. U2.20 - Prob. 6ECh. U2.20 - Prob. 7ECh. U2.20 - Prob. 8ECh. U2.20 - Prob. 9ECh. U2.21 - Prob. 1TAICh. U2.21 - Prob. 1ECh. U2.21 - Prob. 2ECh. U2.21 - Prob. 3ECh. U2.21 - Prob. 4ECh. U2.21 - Prob. 6ECh. U2 - Prob. SI1RECh. U2 - Prob. SI2RECh. U2 - Prob. SI3RECh. U2 - Prob. SI4RECh. U2 - Prob. SI5RECh. U2 - Prob. SII1RECh. U2 - Prob. SII2RECh. U2 - Prob. SII3RECh. U2 - Prob. SII4RECh. U2 - Prob. SII5RECh. U2 - Prob. SIII1RECh. U2 - Prob. SIII2RECh. U2 - Prob. SIII3RECh. U2 - Prob. SIII4RECh. U2 - Prob. SIII5RECh. U2 - Prob. SIII6RECh. U2 - Prob. SIV1ECh. U2 - Prob. SIV2ECh. U2 - Prob. SIV3ECh. U2 - Prob. SIV4ECh. U2 - Prob. SIV5ECh. U2 - Prob. 1RECh. U2 - Prob. 2RECh. U2 - Prob. 3RECh. U2 - Prob. 4RECh. U2 - Prob. 5RECh. U2 - Prob. 6RECh. U2 - Prob. 7RECh. U2 - Prob. 8RE
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