Organic Chemistry: Principles And Mechanisms (second Edition)
Organic Chemistry: Principles And Mechanisms (second Edition)
2nd Edition
ISBN: 9780393630749
Author: KARTY, Joel
Publisher: W. W. Norton & Company
Question
Book Icon
Chapter 24, Problem 24.19P
Interpretation Introduction

(a)

Interpretation:

Whether the given diol can be produced from an alkene using either OsO4 or KMnO4 is to be determined, and the alkene that can be used to produce it is to be drawn.

Concept introduction:

The alkene, on reaction with OsO4 or KMnO4, undergoes syn addition and gives cis-1, 2-diol. Thus the 1, 2- diol, which is able to attain cis confirmation, can be prepared through syn addition using either OsO4 or KMnO4. The carbons having OH groups must have C=C bond in the alkene.

Expert Solution
Check Mark

Answer to Problem 24.19P

The given diol is cis-1, 2-diol; thus can be produced from an alkene using either OsO4 or KMnO4, and the structure of that alkene is

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  1

Explanation of Solution

The given diol is

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  2

The given diol is cis-1, 2-diol as both hydroxyl groups are on the same side of the ring; thus it can be produced from an alkene using either OsO4 or KMnO4. The alkene that can be used to produce this diol is identified by replacing the hydroxyl groups and placing the double bond between those carbons. Therefore, the structure of the alkene is

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  3

Conclusion

It is determined that the diol can be produced using reagents, either OsO4 or KMnO4, by identifying the diol is cis-1, 2-diol, and the structure of the alkene is drawn by placing the double bond between the carbons having OH groups.

Interpretation Introduction

(b)

Interpretation:

Whether the given diol can be produced from an alkene using either OsO4 or KMnO4 is to be determined, and the alkene that can be used to produce it is to be drawn.

Concept introduction:

The alkene, on reaction with OsO4 or KMnO4, undergoes syn addition and gives cis-1, 2-diol. Thus the 1, 2- diol, which is able to attain cis confirmation, can be prepared through syn addition using either OsO4 or KMnO4. The carbons having OH groups must have C=C bond in the alkene.

Expert Solution
Check Mark

Answer to Problem 24.19P

The given diol is not a cis-1, 2-diol; thus it cannot be produced from an alkene using either OsO4 or KMnO4.

Explanation of Solution

The given diol is

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  4

The given diol is not a cis-1, 2-diol as the hydroxyl groups are on the opposite sides of the ring; thus it cannot be produced from an alkene using either OsO4 or KMnO4.

Conclusion

It is determined that the diol cannot be produced using reagents either OsO4 or KMnO4 by identifying that the diol is not cis-1, 2-diol.

Interpretation Introduction

(c)

Interpretation:

Whether the given diol can be produced from an alkene using either OsO4 or KMnO4 is to be determined, and the alkene that can be used to produce it is to be drawn.

Concept introduction:

The alkene, on reaction with OsO4 or KMnO4, undergoes syn addition and gives cis-1, 2-diol. Thus the 1, 2- diol, which is able to attain cis confirmation, can be prepared through syn addition using either OsO4 or KMnO4. The carbons having OH groups must have C=C bond in the alkene.

Expert Solution
Check Mark

Answer to Problem 24.19P

The given diol is not a cis-1, 2-diol; thus it cannot be produced from an alkene using either OsO4 or KMnO4.

Explanation of Solution

The given diol is

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  5

The given diol is not a cis-1, 2-diol as the hydroxyl groups are at 1, 3 positions; thus it cannot be produced from an alkene using either OsO4 or KMnO4.

Conclusion

It is determined that the diol cannot be produced using reagents either OsO4 or KMnO4 by identifying that the diol is not cis-1, 2-diol.

Interpretation Introduction

(d)

Interpretation:

Whether the given diol can be produced from an alkene using either OsO4 or KMnO4 is to be determined, and the alkene that can be used to produce it is to be drawn.

Concept introduction:

The alkene, on reaction with OsO4 or KMnO4, undergoes syn addition and gives cis-1, 2-diol. Thus the 1, 2- diol, which is able to attain cis confirmation, can be prepared through syn addition using either OsO4 or KMnO4. The carbons having OH groups must have C=C bond in the alkene.

Expert Solution
Check Mark

Answer to Problem 24.19P

The given diol is cis-1, 2-diol; thus it can be produced from an alkene using either OsO4 or KMnO4, and the structure of that alkene is

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  6

Explanation of Solution

The given diol is

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  7

The given diol is cis-1, 2-diol as both hydroxyl groups are on the same side of the ring; thus it can be produced from an alkene using either OsO4 or KMnO4. The alkene that can be used to produce this diol is identified by replacing the hydroxyl groups and placing the double bond between those carbons. Therefore, the structure of the alkene is

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  8

Conclusion

It is determined that the diol can be produced using reagents either OsO4 or KMnO4 by identifying that the diol is cis-1, 2-diol, and the structure of the alkene is drawn by placing the double bond between the carbons having OH groups.

Interpretation Introduction

(e)

Interpretation:

Whether the given diol can be produced from an alkene using either OsO4 or KMnO4 is to be determined, and the alkene that can be used to produce it is to be drawn.

Concept introduction:

The alkene, on reaction with OsO4 or KMnO4, undergoes syn addition and gives cis-1, 2-diol. Thus the 1, 2- diol, which is able to attain cis confirmation, can be prepared through syn addition using either OsO4 or KMnO4. The carbons having OH groups must have C=C bond in the alkene.

Expert Solution
Check Mark

Answer to Problem 24.19P

The given diol is 1, 2-diol and is able to attain cis conformation through single bond rotation; thus it can be produced from an alkene using either OsO4 or KMnO4, and the structure of that alkene is

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  9

Explanation of Solution

The given diol is

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  10

The given diol is trans-1, 2-diol as both hydroxyl groups are on opposite sides of the ring, but it can attain the cis confirmation by single bond rotation. Thus, it can be produced from an alkene using either OsO4 or KMnO4.

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  11

The alkene that can be used to produce this diol is identified by replacing the hydroxyl groups and placing the double bond between those carbons. Therefore, the structure of the alkene is

Organic Chemistry: Principles And Mechanisms (second Edition), Chapter 24, Problem 24.19P , additional homework tip  12

Conclusion

It is determined that the diol can be produced using reagents either OsO4 or KMnO4 by identifying that the diol can attain cis-1, 2-diol confirmation, and the structure of alkene is drawn by placing the double bond between the carbons having OH groups.

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
A block of copper of mass 2.00kg(cp = 0.3851 .K) and g temperature 0°C is introduced into an insulated container in which there is 1.00molH, O(g) at 100°C and 1.00 2 atm. Note that C P = 4.184. K for liquid water, and g that A H = 2260 for water. vap g Assuming all the steam is condensed to water, and that the pressure remains constant: (a) What will be the final temperature of the system? (b) What is the heat transferred from the water to the copper? (c) What is the entropy change of the water, the copper, and the total system?
Identify the missing organic reactants in the following reaction: H+ X + Y OH H+ O O Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H₂O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Explanation Check Click and drag to start drawing a structure. X G 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Cente ? E
Calculate the solubility of CaF2 in g/L (Kp = 4.0 x 10-8). sp

Chapter 24 Solutions

Organic Chemistry: Principles And Mechanisms (second Edition)

Ch. 24 - Prob. 24.11PCh. 24 - Prob. 24.12PCh. 24 - Prob. 24.13PCh. 24 - Prob. 24.14PCh. 24 - Prob. 24.15PCh. 24 - Prob. 24.16PCh. 24 - Prob. 24.17PCh. 24 - Prob. 24.18PCh. 24 - Prob. 24.19PCh. 24 - Prob. 24.20PCh. 24 - Prob. 24.21PCh. 24 - Prob. 24.22PCh. 24 - Prob. 24.23PCh. 24 - Prob. 24.24PCh. 24 - Prob. 24.25PCh. 24 - Prob. 24.26PCh. 24 - Prob. 24.27PCh. 24 - Prob. 24.28PCh. 24 - Prob. 24.29PCh. 24 - Prob. 24.30PCh. 24 - Prob. 24.31PCh. 24 - Prob. 24.32PCh. 24 - Prob. 24.33PCh. 24 - Prob. 24.34PCh. 24 - Prob. 24.35PCh. 24 - Prob. 24.36PCh. 24 - Prob. 24.37PCh. 24 - Prob. 24.38PCh. 24 - Prob. 24.39PCh. 24 - Prob. 24.40PCh. 24 - Prob. 24.41PCh. 24 - Prob. 24.42PCh. 24 - Prob. 24.43PCh. 24 - Prob. 24.44PCh. 24 - Prob. 24.45PCh. 24 - Prob. 24.46PCh. 24 - Prob. 24.47PCh. 24 - Prob. 24.48PCh. 24 - Prob. 24.49PCh. 24 - Prob. 24.50PCh. 24 - Prob. 24.51PCh. 24 - Prob. 24.52PCh. 24 - Prob. 24.53PCh. 24 - Prob. 24.54PCh. 24 - Prob. 24.55PCh. 24 - Prob. 24.56PCh. 24 - Prob. 24.57PCh. 24 - Prob. 24.58PCh. 24 - Prob. 24.59PCh. 24 - Prob. 24.60PCh. 24 - Prob. 24.61PCh. 24 - Prob. 24.62PCh. 24 - Prob. 24.63PCh. 24 - Prob. 24.64PCh. 24 - Prob. 24.65PCh. 24 - Prob. 24.66PCh. 24 - Prob. 24.67PCh. 24 - Prob. 24.68PCh. 24 - Prob. 24.69PCh. 24 - Prob. 24.70PCh. 24 - Prob. 24.71PCh. 24 - Prob. 24.72PCh. 24 - Prob. 24.73PCh. 24 - Prob. 24.74PCh. 24 - Prob. 24.75PCh. 24 - Prob. 24.76PCh. 24 - Prob. 24.77PCh. 24 - Prob. 24.78PCh. 24 - Prob. 24.79PCh. 24 - Prob. 24.80PCh. 24 - Prob. 24.81PCh. 24 - Prob. 24.82PCh. 24 - Prob. 24.83PCh. 24 - Prob. 24.84PCh. 24 - Prob. 24.1YTCh. 24 - Prob. 24.2YTCh. 24 - Prob. 24.3YTCh. 24 - Prob. 24.4YTCh. 24 - Prob. 24.5YTCh. 24 - Prob. 24.6YTCh. 24 - Prob. 24.7YTCh. 24 - Prob. 24.8YTCh. 24 - Prob. 24.9YTCh. 24 - Prob. 24.10YTCh. 24 - Prob. 24.11YTCh. 24 - Prob. 24.12YTCh. 24 - Prob. 24.13YTCh. 24 - Prob. 24.14YTCh. 24 - Prob. 24.15YTCh. 24 - Prob. 24.16YTCh. 24 - Prob. 24.17YT
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY