Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
Question
Book Icon
Chapter 10.3A, Problem 10.1P

(a)

Interpretation Introduction

To determine: The IUPAC name of the given alcohol.

Interpretation: The IUPAC name of the given alcohol is to be stated.

Concept introduction: The IUPAC naming of the alcohol are 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 to 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.

(b)

Interpretation Introduction

To determine: The IUPAC name of the given alcohol.

Interpretation: The IUPAC name of the given alcohol is to be stated.

Concept introduction: The IUPAC naming of the alcohol are 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 to 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.

(c)

Interpretation Introduction

To determine: The IUPAC name of the given alcohol.

Interpretation: The IUPAC name of the given alcohol is to be stated.

Concept introduction: The IUPAC naming of the alcohol are 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 to 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.

(d)

Interpretation Introduction

To determine: The IUPAC name of the given alcohol.

Interpretation: The IUPAC name of the given alcohol is to be stated.

Concept introduction: The IUPAC naming of the alcohol are 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 to 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.

(e)

Interpretation Introduction

To determine: The IUPAC name of the given alcohol.

Interpretation: The IUPAC name of the given alcohol is to be stated.

Concept introduction: The IUPAC naming of the alcohol are 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 to 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.

(f)

Interpretation Introduction

To determine: The IUPAC name of the given alcohol.

Interpretation: The IUPAC name of the given alcohol is to be stated.

Concept introduction: The IUPAC naming of the alcohol are 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 to 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.

Blurred answer
Students have asked these similar questions
Give the IUPAC name of the following alcohols
Give the IUPAC name and common name of the following alcohols
Give the IUPAC name of the following alcohols and phenols.

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
Recommended textbooks for you
Text book image
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,
Text book image
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Text book image
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning
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