Organic Chemistry: Principles And Mechanisms
Organic Chemistry: Principles And Mechanisms
2nd Edition
ISBN: 9780393663549
Author: KARTY, Joel
Publisher: W. W. Norton and Company
bartleby

Videos

Question
Book Icon
Chapter F, Problem F.10P
Interpretation Introduction

(a)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

There are two types of acid anhydrides, symmetric and asymmetric. In symmetric acid anhydrides, the alkyl groups bonded to both carbonyl carbons are the same, i.e., formed from dehydration of two molecules of the same carboxylic acid. The general form of symmetric acid anhydride name is alkanoic anhydride. In asymmetric acid anhydrides, the alkyl groups bonded to both carbonyl carbons are different, i.e., formed from dehydration of molecules of different carboxylic acids. The general form of asymmetric acid anhydride name is alkanoic alkanoic anhydride. The two alkanoic groups appear in alphabetical order. The ‘alkanoic’ corresponds to the specific carboxylic acid(s) that undergo dehydration to produce the anhydride. The ‘alkan’ is the root name for the longest chain containing the carbonyl group.

Interpretation Introduction

(b)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

Acid anhydrides are of two types symmetric and asymmetric. In symmetric acid anhydrides, the alkyl groups bonded to both carbonyl carbons are the same i.e. formed from dehydration of two molecules of same carboxylic acid. The general form of symmetric acid anhydride name is alkanoic anhydride. In asymmetric acid anhydrides, the alkyl groups bonded to both carbonyl carbons are different i.e. formed from dehydration of two molecules of different carboxylic acids. The general form of asymmetric acid anhydride name is alkanoic anhydride. The two alkanoic groups appear in alphabetical order. The ‘alkanoic’ corresponds to the specific carboxylic acid(s) that undergo(es) dehydration to produce the anhydride. The ‘alkan’ is the root name stands for the longest chain having the carbonyl group.

Interpretation Introduction

(c)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

Acid anhydrides are of two types, symmetric and asymmetric. In symmetric acid anhydrides, the alkyl groups bonded to both carbonyl carbons are the same, i.e., formed from dehydration of two molecules of the same carboxylic acid. The general form of symmetric acid anhydride name is alkanoic anhydride. In asymmetric acid anhydrides, the alkyl groups bonded to both carbonyl carbons are different, i.e., formed from dehydration of molecules of different carboxylic acids. The general form of asymmetric acid anhydride name is alkanoic alkanoic anhydride. The two alkanoic groups appear in alphabetical order. The ‘alkanoic’ corresponds to the specific carboxylic acid(s) that undergo(es) dehydration to produce the anhydride. The ‘alkan’ is the root name for the longest chain containing the carbonyl group.

Blurred answer
Students have asked these similar questions
Find the pH of a 0.120 M solution of HNO2. Find the pH ignoring activity effects (i.e., the normal way). Find the pH in a solution of 0.050 M NaCl, including activity
Please help me answer these three questions. Required info should be in data table.
Draw the major organic substitution product or products for (2R,3S)-2-bromo-3-methylpentane reacting with the given nucleophile. Clearly drawn the stereochemistry, including a wedged bond, a dashed bond and two in-plane bonds at each stereogenic center. Omit any byproducts. Bri CH3CH2O- (conc.) Draw the major organic product or products.
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 for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:9781938168390
Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:OpenStax
07 Physical Properties of Organic Compounds; Author: Mindset;https://www.youtube.com/watch?v=UjlSgwq4w6U;License: Standard YouTube License, CC-BY