Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
bartleby

Concept explainers

bartleby

Videos

Textbook Question
Book Icon
Chapter 10, Problem 10.30SP

Give a systematic (IUPAC) name for each alcohol. Classify each as primary, secondary, or tertiary.

Chapter 10, Problem 10.30SP, Give a systematic (IUPAC) name for each alcohol. Classify each as primary, secondary, or tertiary. , example  1

Chapter 10, Problem 10.30SP, Give a systematic (IUPAC) name for each alcohol. Classify each as primary, secondary, or tertiary. , example  2

(a)

Expert Solution
Check Mark
Interpretation Introduction

To determine: The systematic (IUPAC) name for the given alcohol and its classification as primary, secondary or tertiary.

Interpretation: The systematic (IUPAC) name for the given alcohol is to be stated and the given alcohol is to be classified as primary, secondary or tertiary.

Concept introduction: The IUPAC nomenclature of alcohols is based on the following rules given below.

  1. 1. The longest carbon chain that contains the carbon atom bearing the OH group is named first and suffix ol is added to the root name.
  2. 2. The longest carbon chain is numbered starting at the end nearest the OH group and number is used to show the position of OH group and it is given preference over double and triple bond in the structure.
  3. 3. All the substituents are named and numbers are given to their position in the longest carbon chain.

Answer to Problem 10.30SP

The IUPAC name of the given alcohol is 5-methyl-4-propylheptan-2-ol. It is classified as secondary alcohol.

Explanation of Solution

The structure of the alcohol is given below.

Organic Chemistry (9th Edition), Chapter 10, Problem 10.30SP , additional homework tip  1

Figure 1

In the given structure of alcohol, the longest carbon chain contains 7 carbon. So root name is heptanol. In the structure, methyl group is attached to 5 carbon and OH group is attached to the 2 carbon in the primary carbon chain. Propyl group is attached to 4 carbon in the longest carbon chain.

So, the IUPAC name of the given alcohol is 5-methyl-4-propylheptan-2-ol.

The hydroxy group is attached to the secondary carbon. So, the given compound is secondary alcohol.

(b)

Expert Solution
Check Mark
Interpretation Introduction

To determine: The systematic (IUPAC) name for the given alcohol and its classification as primary, secondary or tertiary.

Interpretation: The systematic (IUPAC) name for the given alcohol is to be stated and the given alcohol is to be classified as primary, secondary or tertiary.

Concept introduction: The IUPAC nomenclature of alcohols is based on the following rules given below.

  1. 1. The longest carbon chain that contains the carbon atom bearing the OH group is named first and suffix ol is added to the root name.
  2. 2. The longest carbon chain is numbered starting at the end nearest the OH group and number is used to show the position of OH group and it is given preference over double and triple bond in the structure.
  3. 3. All the substituents are named and numbers are given to their position in the longest carbon chain.

Answer to Problem 10.30SP

The IUPAC name of the given alcohol is 4-(1-bromoethyl)heptan-3-ol. It is classified as secondary alcohol.

Explanation of Solution

The structure of the alcohol is given below.

Organic Chemistry (9th Edition), Chapter 10, Problem 10.30SP , additional homework tip  2

Figure 2

In the given structure of alcohol, the longest carbon chain contains 7 carbon. So root name is heptanol. In the structure, 1-bromoethyl group is attached to 4 carbon and OH group is attached to the 3 carbon in the primary carbon chain.

So, the IUPAC name of the given alcohol is 4-(1-bromoethyl)heptan-3-ol.

The hydroxy group is attached to the secondary carbon. So, the given compound is secondary alcohol.

(c)

Expert Solution
Check Mark
Interpretation Introduction

To determine: The systematic (IUPAC) name for the given alcohol and its classification as primary, secondary or tertiary.

Interpretation: The systematic (IUPAC) name for the given alcohol is to be stated and the given alcohol is to be classified as primary, secondary or tertiary.

Concept introduction: The IUPAC nomenclature of alcohols is based on the following rules given below.

  1. 1. The longest carbon chain that contains the carbon atom bearing the OH group is named first and suffix ol is added to the root name.
  2. 2. The longest carbon chain is numbered starting at the end nearest the OH group and number is used to show the position of OH group and it is given preference over double and triple bond in the structure.
  3. 3. All the substituents are named and numbers are given to their position in the longest carbon chain.

Answer to Problem 10.30SP

The IUPAC name of the given alcohol is 6-chloro-3-phenyloctan-3-ol. It is classified as tertiary alcohol.

Explanation of Solution

The structure of the alcohol is given below.

Organic Chemistry (9th Edition), Chapter 10, Problem 10.30SP , additional homework tip  3

Figure 3

In the given structure of alcohol, the longest carbon chain contains 8 carbon atoms. So root name is octanol. In the structure, phenyl group is attached to 3 carbon and OH group is attached to the 3 carbon in the primary carbon chain. Chloro group is attached to the 6 carbon in the primary carbon chain.

So, the IUPAC name of the given alcohol is 6-chloro-3-phenyloctan-3-ol.

The hydroxy group is attached to the tertiary carbon. So, the given compound is tertiary alcohol.

(d)

Expert Solution
Check Mark
Interpretation Introduction

To determine: The systematic (IUPAC) name for the given alcohol and its classification as primary, secondary or tertiary.

Interpretation: The systematic (IUPAC) name for the given alcohol is to be stated and the given alcohol is to be classified as primary, secondary or tertiary.

Concept introduction: The IUPAC nomenclature of alcohols is based on the following rules given below.

  1. 1. The longest carbon chain that contains the carbon atom bearing the OH group is named first and suffix ol is added to the root name.
  2. 2. The longest carbon chain is numbered starting at the end nearest the OH group and number is used to show the position of OH group and it is given preference over double and triple bond in the structure.
  3. 3. All the substituents are named and numbers are given to their position in the longest carbon chain.

Answer to Problem 10.30SP

The IUPAC name of the given alcohol is 3-bromocyclohex-3-ene-1-ol. It is classified as secondary alcohol.

Explanation of Solution

The structure of the alcohol is given below.

Organic Chemistry (9th Edition), Chapter 10, Problem 10.30SP , additional homework tip  4

Figure 4

In the above figure, the structure of cyclo alcohol is shown.

In the given structure of cyclo alcohol, the longest carbon chain contains 6 carbon. So root name is cyclohexanol. In the structure, bromo group is attached to the 3 carbon and OH group is attached to the 1 carbon in the primary carbon chain. The double bond is present between 3 and 4 carbon atoms in the primary carbon chain in the cyclo alcohol.

So, the IUPAC name of the given alcohol is 3-bromocyclohex-3-ene-1-ol.

The hydroxy group is attached to the secondary carbon. So, the given compound is secondary alcohol.

(e)

Expert Solution
Check Mark
Interpretation Introduction

To determine: The systematic (IUPAC) name for the given alcohol and its classification as primary, secondary or tertiary.

Interpretation: The systematic (IUPAC) name for the given alcohol is to be stated and the given alcohol is to be classified as primary, secondary or tertiary.

Concept introduction: The IUPAC nomenclature of alcohols is based on the following rules given below.

  1. 1. The longest carbon chain that contains the carbon atom bearing the OH group is named first and suffix ol is added to the root name.
  2. 2. The longest carbon chain is numbered starting at the end nearest the OH group and number is used to show the position of OH group and it is given preference over double and triple bond in the structure.
  3. 3. All the substituents are named and numbers are given to their position in the longest carbon chain.

Answer to Problem 10.30SP

The IUPAC name of the given alcohol is cis-4-chlorocyclohex-2-ene-1-ol. It is classified as secondary alcohol.

Explanation of Solution

The structure of the alcohol is given below.

Organic Chemistry (9th Edition), Chapter 10, Problem 10.30SP , additional homework tip  5

Figure 5

In the above figure, the structure of cyclo alcohol is shown.

In the given structure of cyclo alcohol, the longest carbon chain contains 6 carbon. So root name is cyclohexanol. In the structure, chloro group is attached to the 4 carbon and OH group is attached to the 1 carbon in the primary carbon chain. Chloro and OH groups are on the same side or cis to each other in the cyclohexanol structure.

The double bond is present between 2 and 3 carbon atoms in the primary carbon chain in the cyclo alcohol.

So, the IUPAC name of the given alcohol is cis-4-chlorocyclohex-2-ene-1-ol.

The hydroxy group is attached to the secondary carbon. So, the given compound is secondary alcohol.

(f)

Expert Solution
Check Mark
Interpretation Introduction

To determine: The systematic (IUPAC) name for the given alcohol and its classification as primary, secondary or tertiary.

Interpretation: The systematic (IUPAC) name for the given alcohol is to be stated and the given alcohol is to be classified as primary, secondary or tertiary.

Concept introduction: The IUPAC nomenclature of alcohols is based on the following rules given below.

  1. 1. The longest carbon chain that contains the carbon atom bearing the OH group is named first and suffix ol is added to the root name.
  2. 2. The longest carbon chain is numbered starting at the end nearest the OH group and number is used to show the position of OH group and it is given preference over double and triple bond in the structure.
  3. 3. All the substituents are named and numbers are given to their position in the longest carbon chain.

Answer to Problem 10.30SP

The IUPAC name of the given alcohol is (E)-4,5-dimethylhex-3-ene-1-ol. It is classified as primary alcohol.

Explanation of Solution

The structure of the alcohol is given below.

Organic Chemistry (9th Edition), Chapter 10, Problem 10.30SP , additional homework tip  6

Figure 6

In the given structure of alcohol, the longest carbon chain contains 6 carbon. So root name is hexanol. In the structure, one methyl group is attached to 4 carbon and second methyl group is attached to 5 carbon. OH group is attached to the 1 carbon in the primary carbon chain.

The double bond is present between 3 and 4 carbon atoms in the primary carbon chain in the cyclo alcohol.

The highest priority groups are opposite to each other. So, the configuration at 3 carbon (double bond) is E.

So, the IUPAC name of the given alcohol is (E)-4,5-dimethylhex-3-ene-1-ol.

The hydroxy group is attached to the primary carbon. So, the given compound is primary alcohol.

(g)

Expert Solution
Check Mark
Interpretation Introduction

To determine: The systematic (IUPAC) name for the given alcohol and its classification as primary, secondary or tertiary.

Interpretation: The systematic (IUPAC) name for the given alcohol is to be stated and the given alcohol is to be classified as primary, secondary or tertiary.

Concept introduction: The IUPAC nomenclature of alcohols is based on the following rules given below.

  1. 1. The longest carbon chain that contains the carbon atom bearing the OH group is named first and suffix ol is added to the root name.
  2. 2. The longest carbon chain is numbered starting at the end nearest the OH group and number is used to show the position of OH group and it is given preference over double and triple bond in the structure.
  3. 3. All the substituents are named and numbers are given to their position in the longest carbon chain.

Answer to Problem 10.30SP

The IUPAC name of the given alcohol is (1-cyclopentenyl) methanol. It is classified as primary alcohol.

Explanation of Solution

The structure of the alcohol is given below.

Organic Chemistry (9th Edition), Chapter 10, Problem 10.30SP , additional homework tip  7

Figure 7

In the given structure of alcohol, the longest carbon chain contains 1 carbon. So root name is methanol. In the structure, cyclopentyl group and OH group are attached to the 1 carbon in the primary carbon chain. The double bond is present between 1 and 2 carbon atoms in the structure of cyclopentyl group.

So, the IUPAC name of the given alcohol is (1-cyclopentenyl)methanol.

The hydroxy group is attached to the primary carbon. So, the given compound is primary alcohol.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
Give the common name for NN OH T CH3-CH₂-C-N-CH₂-CH3 Spell out the common name of the compound. Give the IUPAC name for 0 CH₂ || CH₂-C-N-CH₂-CH₂-CH₂, Spell out the IUPAC name of the compound. diethylamine Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. HE CONT HO
Give systematic (IUPAC) name for each compound. H₂C-Cl IUPAC name: CH3 HỌC–CH–CH,-CH-CH,CH, B,C-CH-CH Cl IUPAC name: CHIC IUPAC name:
Provide the IUPAC name for the structure shown below. (Note: rather than trying to enter greek letters required in the name you can use a to represent a and b to represent B in your answer). CH2OH CH2OH OH ОН ОН OH ОН OH

Chapter 10 Solutions

Organic Chemistry (9th Edition)

Ch. 10.8B - Prob. 10.11PCh. 10.8B - Prob. 10.12PCh. 10.9A - Prob. 10.13PCh. 10.9B - Prob. 10.14PCh. 10.9C - Show how you would synthesize each tertiary...Ch. 10.9D - Prob. 10.16PCh. 10.9D - Show how you would add Grignard reagents to acid...Ch. 10.9D - A formate ester, such as ethyl formate, reacts...Ch. 10.9E - Prob. 10.19PCh. 10.9E - In Section9-7B, we saw how acetylide ions add to...Ch. 10.9F - Prob. 10.21PCh. 10.10A - Prob. 10.22PCh. 10.10B - Prob. 10.23PCh. 10.11B - Predict the products you would expect from the...Ch. 10.11B - Prob. 10.25PCh. 10.11B - Prob. 10.26PCh. 10.12 - Prob. 10.27PCh. 10.12 - Prob. 10.28PCh. 10.12 - Authentic skunk spray has become valuable for use...Ch. 10 - Give a systematic (IUPAC) name for each alcohol....Ch. 10 - Give systematic (IUPAC) names for the following...Ch. 10 - Draw the structures of the following compounds...Ch. 10 - Predict which member of each pair has the higher...Ch. 10 - Predict which member of each pair is more acidic,...Ch. 10 - Predict which member of each group is most soluble...Ch. 10 - Draw the organic products you would expect to...Ch. 10 - Prob. 10.37SPCh. 10 - Show how you would synthesize the following...Ch. 10 - Show how you would use Grignard syntheses to...Ch. 10 - Show how you would accomplish the following...Ch. 10 - Show how you would synthesize the following: a....Ch. 10 - Complete the following acid-base reactions. In...Ch. 10 - Prob. 10.43SPCh. 10 - Prob. 10.44SPCh. 10 - Geminal diols, or 1,1-diols, are usually unstable,...Ch. 10 - Vinyl alcohols are generally unstable, quickly...Ch. 10 - Compound A (C7H11Br) is treated with magnesium in...Ch. 10 - Prob. 10.48SPCh. 10 - Prob. 10.49SPCh. 10 - Prob. 10.50SPCh. 10 - Prob. 10.51SPCh. 10 - Prob. 10.52SPCh. 10 - Prob. 10.53SPCh. 10 - Prob. 10.54SPCh. 10 - Prob. 10.55SPCh. 10 - Prob. 10.56SPCh. 10 - Show how this 1 alcohol can be made from the...Ch. 10 - Prob. 10.58SPCh. 10 - Prob. 10.59SPCh. 10 - Prob. 10.60SP
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Nomenclature: Crash Course Chemistry #44; Author: CrashCourse;https://www.youtube.com/watch?v=U7wavimfNFE;License: Standard YouTube License, CC-BY