Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card
Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card
9th Edition
ISBN: 9781305780170
Author: John E. McMurry
Publisher: Cengage Learning
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Chapter 17.SE, Problem 20VC

Give IUPAC names for the following compounds:

Chapter 17.SE, Problem 20VC, Give IUPAC names for the following compounds:

Expert Solution
Check Mark
Interpretation Introduction

a)

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  1

Interpretation:

To give the IUPAC name of the compound given.

Concept introduction:

Alcohols are named as derivatives of the parent alkane using the suffix–ol. The longest carbon chain containing the hydroxyl group is chosen and the parent name is derived by replacing the ending–e with–ol. The akane chain is numbered beginning at the end nearer to the hydroxyl group. The substituents are numbered according to their position on the chain. The name is written listing the substituents in the alphabetical order and indicating the position to which –OH is bonded.

If the compound is chiral then there can be two types of arrangements of the four groups attached to the chiral carbon, R and S. The four groups are arranged in the order of priority as 1,2,3 and 4 following sequence rules. The molecule is viewed by orienting the group of lowest priority (4) points away from the observer. If the arrangement of highest to second highest to third highest is clockwise the R configuration is assigned. If the arrangement is anticlockwise then S configurationis assigned.

To give:

The IUPAC name of the compound given.

Answer to Problem 20VC

The compound given is

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  2

Its IUPAC name is (R) - 5 methylhexan-3-ol.

Explanation of Solution

The name of the compound indicates the presence of a six carbon straight chain with –OH on C3 and a methyl group on C5. Further the molecule is chiral. The groups –OH (highest ranking), -CH2CH(CH3)2(second highest ranking) and -CH2CH3(third highest ranking) are arranged around the chiral carbon in clockwise arrangement. Hence R configuration is assigned.

Conclusion

The compound given is

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  3

Its IUPAC name is (R) - 5 methylhexan-3-ol.

Expert Solution
Check Mark
Interpretation Introduction

b)

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  4

Interpretation:

To give the IUPAC name of the compound given.

Concept introduction:

In naming cyclic alcohols the parent name is derived from the cycloalkene ring by replacing–e of the cycloalkene with–ol. The ring is numbered from the carbon with –OH in such a way that lowest number possible is given to the carbons with substituents.

A cis 1,3-disubstituted cycloalkane has the two substituent groups in a diequatorial arrangement.

To give:

The IUPAC name of the compound given.

Answer to Problem 20VC

The compound given is

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  5

Its IUPAC name is cis-3-methylcyclohexanol.

Explanation of Solution

The structure shows that the compound contains a cyclohexane ring with a –OH and methyl groups in diequatorial positions on C1 and C3. Hence it is a cis-isomer.

Conclusion

The compound given is

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  6

Its IUPAC name is cis-3-methylcyclohexanol.

Expert Solution
Check Mark
Interpretation Introduction

c)

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  7

Interpretation:

To give the IUPAC name of the compound given.

Concept introduction:

Alcohols are named as derivatives of the parent alkane using the suffix–ol. The longest carbon chain containing the hydroxyl group is chosen and the parent name is derived by replacing the ending–e with–ol. He akane chain is numbered beginning at the end nearer to the hydroxyl group. The substituents are numbered according to their position on the chain. The name is written listing the substituents in the alphabetical order and indicating the position to which –OH is bonded.

If the compound is chiral then there can be two types of arrangements of the four groups attached to the chiral carbon, R and S. The four groups are arranged in the order of priority as 1,2,3 and 4 following sequence rules. The molecule is viewed by orienting the group of lowest priority (4) points away from the observer. If the arrangement of highest to second highest to third highest is clockwise the R configuration is assigned. If the arrangement is anticlockwise then S configurationis assigned.

To give:

The IUPAC name of the compound given.

Answer to Problem 20VC

The compound given is

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  8

Its IUPAC name is (S)-1-cyclopentylethanol.

Explanation of Solution

The structure shows that the compound contains a two carbon straight chain with –OH and a cyclopentyl groups on C1.

The four groups, -OH(Highest priority), Cyclopentyl (second highest priority), methyl (third highest priority) attached to C1 are arranged anticlockwise when viewed away from hydrogen (fourth priority). Hence S configuration is assigned.

Conclusion

The compound given is

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  9

Its IUPAC name is (S)-1-cyclopentylethanol.

Expert Solution
Check Mark
Interpretation Introduction

d)

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  10

Interpretation:

To give the IUPAC name of the compound given.

Concept introduction:

Hydroxybenzenes are named as derivatives of phenol. If the ring contains other substituent also the ring is numbered from the carbon with –OH in such a way that lowest number possible is given to the carbon with the substituent. While writing the name the substituents are arranged in the alphabetical order.

To give:

The IUPAC name of the compound given.

Answer to Problem 20VC

The compound given is.

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  11

Its IUPAC name is 4-methyl-3-nitrophenol.

Explanation of Solution

The structure of the compound shows a benzene ring with –OH on C1, a nitro group on C3 and a methyl group on C4.

Conclusion

The compound given is.

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card, Chapter 17.SE, Problem 20VC , additional homework tip  12

Its IUPAC name is 4-methyl-3-nitrophenol.

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Chapter 17 Solutions

Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card

Ch. 17.5 - Use the reaction of a Grignard reagent with a...Ch. 17.6 - How would you carry out the following...Ch. 17.6 - What products(s) would you expect from dehydration...Ch. 17.7 - What alcohols would give the following products on...Ch. 17.7 - What products would you expect from oxidation of...Ch. 17.8 - TMS ethers can be removed by treatment with...Ch. 17.9 - Show the mechanism for the reaction of...Ch. 17.11 - Prob. 18PCh. 17.11 - When the 1HNMR spectrum of an alcohol is run in...Ch. 17.SE - Give IUPAC names for the following compounds:Ch. 17.SE - Draw the structure of the carbonyl compound(s)...Ch. 17.SE - Prob. 22VCCh. 17.SE - Prob. 23VCCh. 17.SE - Name and assign R or S stereochemistry to the...Ch. 17.SE - Evidence for the intermediate carbocations in the...Ch. 17.SE - Acid-catalyzed dehydration of 2,...Ch. 17.SE - Prob. 27MPCh. 17.SE - Treatment of the following epoxide with aqueous...Ch. 17.SE - Prob. 29MPCh. 17.SE - Prob. 30MPCh. 17.SE - Identify the type of substitution mechanism (SN1,...Ch. 17.SE - The conversion of 3 alcohols into alkenes under...Ch. 17.SE - Prob. 33MPCh. 17.SE - The trimethylsilyl (TMS) protecting group is one...Ch. 17.SE - When the alcohol below is treated with POCI3 and...Ch. 17.SE - Phenols generally have lower pKa’s than...Ch. 17.SE - Give IUPAC names for the following compounds:Ch. 17.SE - Draw and name the eight isomeric alcohols with...Ch. 17.SE - Prob. 39APCh. 17.SE - Named bombykol, the sex pheromone secreted by the...Ch. 17.SE - Carvacrol is a naturally occurring substance...Ch. 17.SE - What Grignard reagent and what carbonyl compound...Ch. 17.SE - What carbonyl compounds would you reduce to...Ch. 17.SE - What carbonyl compounds might you start with to...Ch. 17.SE - Prob. 45APCh. 17.SE - What products would you obtain from reaction of...Ch. 17.SE - Prob. 47APCh. 17.SE - How would you prepare the following compounds from...Ch. 17.SE - Prob. 49APCh. 17.SE - What products would you expect to obtain from...Ch. 17.SE - Prob. 51APCh. 17.SE - Propose structures for alcohols that have the...Ch. 17.SE - Propose a structure consistent with the following...Ch. 17.SE - The 1HNMR spectrum shown is that of...Ch. 17.SE - A compound of unknown structure gave the following...Ch. 17.SE - Propose a structure for a compound C15H24O that...Ch. 17.SE - Prob. 57APCh. 17.SE - Prob. 58APCh. 17.SE - Rank the following substituted phenols in order of...Ch. 17.SE - Benzvl chloride can be converted into benzaldehvde...Ch. 17.SE - Prob. 61APCh. 17.SE - Prob. 62APCh. 17.SE - Prob. 63APCh. 17.SE - Prob. 64APCh. 17.SE - Prob. 65APCh. 17.SE - Prob. 66APCh. 17.SE - Dehydration of trans-2-methylcyclopentanol with...Ch. 17.SE - 2, 3-Dimethyl-2, 3-butanediol has the common name...Ch. 17.SE - As a rule, axial alcohols oxidize somewhat faster...Ch. 17.SE - Prob. 70APCh. 17.SE - A problem often encountered in the oxidation of...Ch. 17.SE - Identify the reagents a-f in the Following scheme:Ch. 17.SE - Prob. 73APCh. 17.SE - Prob. 74APCh. 17.SE - Compound A, C8H10O, has the IR and 1H NMR spectra...Ch. 17.SE - Prob. 76APCh. 17.SE - Prob. 77AP
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