Pearson eText Organic Chemistry -- Instant Access (Pearson+)
Pearson eText Organic Chemistry -- Instant Access (Pearson+)
9th Edition
ISBN: 9780135213728
Author: Leroy Wade, Jan 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
Please help me with # 4 and 5. Thanks in advance!
A small artisanal cheesemaker is testing the acidity of their milk before it coagulates. During fermentation, bacteria produce lactic acid (K₁ = 1.4 x 104), a weak acid that helps to curdle the milk and develop flavor. The cheesemaker has measured that the developing mixture contains lactic acid at an initial concentration of 0.025 M. Your task is to calculate the pH of this mixture and determine whether it meets the required acidity for proper cheese development. To achieve the best flavor, texture and reduce/control microbial growth, the pH range needs to be between pH 4.6 and 5.0. Assumptions: Lactic acid is a monoprotic acid H H :0:0: H-C-C H :0: O-H Figure 1: Lewis Structure for Lactic Acid For simplicity, you can use the generic formula HA to represent the acid You can assume lactic acid dissociation is in water as milk is mostly water. Temperature is 25°C 1. Write the K, expression for the dissociation of lactic acid in the space provided. Do not forget to include state symbols.…
Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. :0: :0 H. 0:0 :0: :6: S: :0: Select to Edit Arrows ::0 Select to Edit Arrows H :0: H :CI: Rotation Select to Edit Arrows H. < :0: :0: :0: S:

Chapter 10 Solutions

Pearson eText Organic Chemistry -- Instant Access (Pearson+)

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
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
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
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Text book image
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
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