EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
2nd Edition
ISBN: 9780393543971
Author: KARTY
Publisher: VST
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
Draw the stepwise mechanism for the reactions
Part I. a) Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone b) Pinacol (2,3-dimethyl, 1-3-butanediol) on treatment w/ acid gives a mixture of pina colone (3,3-dimethyl-2-butanone) and 2, 3-dimethyl - 1,3-butadiene. Give reasonable mechanism the formation of the products For
3. The explosive decomposition of 2 mole of TNT (2,4,6-trinitrotoluene) is shown below: Assume the C(s) is soot-basically atomic carbon (although it isn't actually atomic carbon in real life). 2 CH3 H NO2 NO2 3N2 (g)+7CO (g) + 5H₂O (g) + 7C (s) H a. Use bond dissociation energies to calculate how much AU is for this reaction in kJ/mol.
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