Organic Chemistry: Principles and Mechanisms (Second Edition)
Organic Chemistry: Principles and Mechanisms (Second Edition)
2nd Edition
ISBN: 9780393663556
Author: Joel Karty
Publisher: W. W. Norton & Company
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 5, Problem 5.51P
Interpretation Introduction

(a)

Interpretation:

Zigzag conformation of the given molecule is to be drawn.

Concept introduction:

A zigzag conformation of an acyclic molecule is a representation in which the root carbon chain is represented by a zigzag line in the plane of the paper, and the substituents are shown above or below the plane by using wedge and dash bonds.

If the OH groups on adjacent asymmetric carbon atoms are on the same side in the Fischer projection, they appear on opposite sides in the zigzag conformation – one of them on a dash bond and the other on a wedge bond. If they are on the opposite sides in the Fischer projection, they appear on the same side in the zigzag conformation, both on dash bonds or both on wedge bonds.

Interpretation Introduction

Interpretation:

(b)

Zigzag conformation of the given molecule is to be drawn.

Concept introduction:

A zigzag conformation of an acyclic molecule is a representation in which the root carbon chain is represented by a zigzag line in the plane of the paper, and the substituents are shown above or below the plane by using wedge and dash bonds.

If the OH groups on adjacent asymmetric carbon atoms are on the same side in the Fischer projection, they appear on opposite sides in the zigzag conformation – one of them on a dash bond and the other on a wedge bond. If they are on the opposite sides in the Fischer projection, they appear on the same side in the zigzag conformation, both on dash bonds or both on wedge bonds.

Interpretation Introduction

Interpretation:

(c)

Zigzag conformation of the given molecule is to be drawn.

Concept introduction:

A zigzag conformation of an acyclic molecule is a representation in which the root carbon chain is represented by a zigzag line in the plane of the paper, and the substituents are shown above or below the plane by using wedge and dash bonds.

If the OH groups on adjacent asymmetric carbon atoms are on the same side in the Fischer projection, they appear on opposite sides in the zigzag conformation – one of them on a dash bond and the other on a wedge bond. If they are on the opposite sides in the Fischer projection, they appear on the same side in the zigzag conformation, both on dash bonds or both on wedge bonds.

Interpretation Introduction

Interpretation:

(d)

Zigzag conformation of the given molecule is to be drawn.

Concept introduction:

A zigzag conformation of an acyclic molecule is a representation in which the root carbon chain is represented by a zigzag line in the plane of the paper, and the substituents are shown above or below the plane by using wedge and dash bonds.

If the OH groups on adjacent asymmetric carbon atoms are on the same side in the Fischer projection, they appear on opposite sides in the zigzag conformation – one of them on a dash bond and the other on a wedge bond. If they are on the opposite sides in the Fischer projection, they appear on the same side in the zigzag conformation, both on dash bonds or both on wedge bonds.

Blurred answer
Students have asked these similar questions
22
PLEASE READ!!! I DONT WANT EXAMPLES, I DONT WANT WORDS OR PARAGRAPHS FOR THE MECHANISM!!! THANKS First image: QUESTION 6. I have to show, with ARROWS and STRUCTURES, the mechanism of the reaction at the bottom. Also I have to show by mecanism why the reaction wouldn't work if the alcohol was primary. I also tried to draw the mechanism, tell me what to change. Please note that its an AMIDE thats formed not an AMINE the nitrogen has ONE hydrogen and one Phenyl-C-Phenyl. I already asked for this mechanism and got as a final product ...-NH2 not whats shown on the picture, thank you Ths second part. QUESTION 3. I just need a way to synthesize the lactone A, I already started please continue from where I left it  Second image: I simply need the products, substrates or reagents, thank you
Indicate how to prepare a 10% sodium hydroxide (NaOH) solution to a slightly alkaline pH.

Chapter 5 Solutions

Organic Chemistry: Principles and Mechanisms (Second Edition)

Ch. 5 - Prob. 5.11PCh. 5 - Prob. 5.12PCh. 5 - Prob. 5.13PCh. 5 - Prob. 5.14PCh. 5 - Prob. 5.15PCh. 5 - Prob. 5.16PCh. 5 - Prob. 5.17PCh. 5 - Prob. 5.18PCh. 5 - Prob. 5.19PCh. 5 - Prob. 5.20PCh. 5 - Prob. 5.21PCh. 5 - Prob. 5.22PCh. 5 - Prob. 5.23PCh. 5 - Prob. 5.24PCh. 5 - Prob. 5.25PCh. 5 - Prob. 5.26PCh. 5 - Prob. 5.27PCh. 5 - Prob. 5.28PCh. 5 - Prob. 5.29PCh. 5 - Prob. 5.30PCh. 5 - Prob. 5.31PCh. 5 - Prob. 5.32PCh. 5 - Prob. 5.33PCh. 5 - Prob. 5.34PCh. 5 - Prob. 5.35PCh. 5 - Prob. 5.36PCh. 5 - Prob. 5.37PCh. 5 - Prob. 5.38PCh. 5 - Prob. 5.39PCh. 5 - Prob. 5.40PCh. 5 - Prob. 5.41PCh. 5 - Prob. 5.42PCh. 5 - Prob. 5.43PCh. 5 - Prob. 5.44PCh. 5 - Prob. 5.45PCh. 5 - Prob. 5.46PCh. 5 - Prob. 5.47PCh. 5 - Prob. 5.48PCh. 5 - Prob. 5.49PCh. 5 - Prob. 5.50PCh. 5 - Prob. 5.51PCh. 5 - Prob. 5.52PCh. 5 - Prob. 5.53PCh. 5 - Prob. 5.54PCh. 5 - Prob. 5.55PCh. 5 - Prob. 5.56PCh. 5 - Prob. 5.57PCh. 5 - Prob. 5.58PCh. 5 - Prob. 5.59PCh. 5 - Prob. 5.60PCh. 5 - Prob. 5.61PCh. 5 - Prob. 5.62PCh. 5 - Prob. 5.63PCh. 5 - Prob. 5.64PCh. 5 - Prob. 5.65PCh. 5 - Prob. 5.66PCh. 5 - Prob. 5.67PCh. 5 - Prob. 5.68PCh. 5 - Prob. 5.69PCh. 5 - Prob. 5.70PCh. 5 - Prob. 5.71PCh. 5 - Prob. 5.72PCh. 5 - Prob. 5.73PCh. 5 - Prob. 5.74PCh. 5 - Prob. 5.75PCh. 5 - Prob. 5.76PCh. 5 - Prob. 5.77PCh. 5 - Prob. 5.78PCh. 5 - Prob. 5.79PCh. 5 - Prob. 5.1YTCh. 5 - Prob. 5.2YTCh. 5 - Prob. 5.3YTCh. 5 - Prob. 5.4YTCh. 5 - Prob. 5.5YTCh. 5 - Prob. 5.6YTCh. 5 - Prob. 5.7YTCh. 5 - Prob. 5.8YTCh. 5 - Prob. 5.9YTCh. 5 - Prob. 5.10YTCh. 5 - Prob. 5.11YTCh. 5 - Prob. 5.12YTCh. 5 - Prob. 5.13YTCh. 5 - Prob. 5.14YTCh. 5 - Prob. 5.15YTCh. 5 - Prob. 5.16YTCh. 5 - Prob. 5.17YT
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
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Chapter 4 Alkanes and Cycloalkanes Lesson 2; Author: Linda Hanson;https://www.youtube.com/watch?v=AL_CM_Btef4;License: Standard YouTube License, CC-BY
Chapter 4 Alkanes and Cycloalkanes Lesson 1; Author: Linda Hanson;https://www.youtube.com/watch?v=PPIa6EHJMJw;License: Standard Youtube License