Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
2nd Edition
ISBN: 9780393655551
Author: KARTY, Joel
Publisher: W. W. Norton & Company
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter A, Problem A.34P
Interpretation Introduction

(a)

Interpretation:

The structure of 2-cyclopropoxypentane is to be drawn.

Concept introduction:

The root name of the longest carbon chain is the alkane name at the end of the compound’s name. The names of the substituents along with numbers indicate their positions on the longest carbon chain. A prefix of the substituent name shows their numbers. The oxygen atom is attached to the alkyl group. The name of the oxygen atom attached to the alkyl group is alkoxy group.

Interpretation Introduction

(b)

Interpretation:

The structure of 1, 2-dimethoxy-4-propylcyclohexane is to be drawn.

Concept introduction:

The root name of the longest carbon chain is the alkane name at the end of the compound’s name. The names of the substituents along with numbers indicate their positions on the longest carbon chain. A prefix of the substituent name shows their numbers. The oxygen atom is attached to the alkyl group. The name of the oxygen atom attached to the alkyl group is alkoxy group.

Interpretation Introduction

(c)

Interpretation:

The structure of 4-(1, 1-dimethylethyl)-1, 2-dipropoxycyclooctane  is to be drawn.

Concept introduction:

The root name of the longest carbon chain is the alkane name at the end of the compound’s name. The names of the substituents along with numbers indicate their positions on the longest carbon chain. A prefix of the substituent name shows their numbers. The oxygen atom is attached to the alkyl group. The name of the oxygen atom attached to the alkyl group is alkoxy group.

Blurred answer
Students have asked these similar questions
Draw the structure corresponding to each IUPAC name. a.3-ethyl-2-methylhexane b. sec-butylcyclopentane c.4-isopropyl-2,4,5-trimethylundecane d.cyclobutylcycloheptane e.3-ethyl-1,1-dimethylcyclohexane f. 4-butyl-1,1-diethylcyclooctane g.6-isopropyl-2,3-dimethyldodecane h. 2,2,6,6,7-pentamethyloctane i. cis-1-ethyl-3-methylcyclopentane j. trans-1-tert-butyl-4-ethylcyclohexane
Each of the following IUPAC names is incorrect. Explain why it is incorrect and give the correct IUPAC name. a. 4-methylpentane b. 2,3,3-trimethylbutane c. 1,3-dimethylpentane d. 3-methyl-5-ethylhexane e. 2-ethyl-2-methylcycloheptane f. 1,6-diethylcyclohexane
CH3 2. Give the structure corresponding to each IUPAC name. a. 3-ethyl-3-methylhexane b. 2-ethyl-1-methyl-3-propylcyclopentane c. 3-methylbutane d. 1-ethyl-2,3-dimethylcyclopentane e. 1,5-dimethylcyclohexane
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
Introductory Chemistry For Today
Chemistry
ISBN:9781285644561
Author:Seager
Publisher:Cengage
Text book image
Chemistry: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co
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
Nomenclature: Crash Course Chemistry #44; Author: CrashCourse;https://www.youtube.com/watch?v=U7wavimfNFE;License: Standard YouTube License, CC-BY