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 A, Problem A.17P
Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the ter-butyl ethyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name of the cyclohexyl methyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(c)

Interpretation:

The IUPAC name of sec-butyl propyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Blurred answer
Students have asked these similar questions
Explain what is the maximum absorbance of in which caffeine absorbs?
Explain reasons as to why the amount of caffeine extracted from both a singular extraction (5ml Mountain Dew) and a multiple extraction (2 x 5.0ml Mountain Dew) were severely high when compared to coca-cola?
Protecting Groups and Carbonyls 6) The synthesis generates allethrolone that exhibits high insect toxicity but low mammalian toxicity. They are used in pet shampoo, human lice shampoo, and industrial sprays for insects and mosquitos. Propose detailed mechanistic steps to generate the allethrolone label the different types of reagents (Grignard, acid/base protonation, acid/base deprotonation, reduction, oxidation, witting, aldol condensation, Robinson annulation, etc.) III + VI HS HS H+ CH,CH,Li III I II IV CI + P(Ph)3 V ༼ Hint: no strong base added VI S VII IX HO VIII -MgBr HgCl2,HgO HO. isomerization aqeuous solution H,SO, ༽༽༤༽༽ X MeOH Hint: enhances selectivity for reaction at the S X ☑
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: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Text book image
Chemistry In Focus
Chemistry
ISBN:9781337399692
Author:Tro, Nivaldo J.
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