Chemistry: The Molecular Nature of Matter and Change - Standalone book
Chemistry: The Molecular Nature of Matter and Change - Standalone book
7th Edition
ISBN: 9780073511177
Author: Martin Silberberg Dr., Patricia Amateis Professor
Publisher: McGraw-Hill Education
bartleby

Concept explainers

Introduction to Organic Chemistry
The field of chemistry which deals with the studies of reactions, structures, and properties of organic compounds that comprise carbon bonded through covalent bonding is organic chemistry. The studies regarding the structure of organic compounds could be…
Vinyl Group
Vinyl group is the name given to the functional group of -CH=CH2. It can be seen as an ethene molecule with one less hydrogen in number. Hence it is also called as ethenyl group at times.
Straight Chain Hydrocarbons
The requirement to identify each compound needs a richer number of words than informative prefixes like n and iso. The identification of organic molecules is made easier by the use of systematic nomenclature schemes. The organic chemistry nomenclature ha…
Unsaturated Hydrocarbon
Following are few examples of alkenes with their general molecular as well as their structural formulas:
Conjugated Compounds in Organic Chemistry
The delocalization of electrons in a molecule is called conjugation in organic chemistry. This delocalisation process of electrons leads to the shortenings or elongations of chemical bonds, but at the same time it causes changes in the chemical propertie…
Alpha Carbon And Alpha Protons
The carbon directly attached to the functional group in an organic molecule is referred to as the alpha carbon and the hydrogen attached to an alpha carbon are termed as the alpha hydrogens or alpha protons. These alpha carbon atoms and alpha hydrogen at…
Question
Book Icon
Chapter 15, Problem 15.69P

(a)

Interpretation Introduction

Interpretation:

The condensed formula for the carboxylic acid and alcohol that forms ethyl hexanoate has to be drawn.

Concept Introduction:

Fischer Esterification:

When an acid is reacted with an alcohol in presence of strong acid catalyst, it forms an ester.

Chemistry: The Molecular Nature of Matter and Change - Standalone book, Chapter 15, Problem 15.69P , additional homework tip 1

The condensed formula is a way of representing an organic compound formula in a single line without the vertical bonds.  In condensed formula each carbon atom is grouped with its hydrogens, but all bonds are not shown.

(b)

Interpretation Introduction

Interpretation:

The condensed formula for the carboxylic acid and alcohol that forms propyl benzoate has to be drawn.

Concept Introduction:

Fischer Esterification:

When an acid is reacted with an alcohol in presence of strong acid catalyst, it forms an ester.

Chemistry: The Molecular Nature of Matter and Change - Standalone book, Chapter 15, Problem 15.69P , additional homework tip 2

The condensed formula is a way of representing an organic compound formula in a single line without the vertical bonds.  In condensed formula each carbon atom is grouped with its hydrogens, but all bonds are not shown.

(c)

Interpretation Introduction

Interpretation:

The condensed formula for the carboxylic acid and alcohol that forms ethyl-3-phenylpropionate has to be drawn.

Concept Introduction:

Fischer Esterification:

When an acid is reacted with an alcohol in presence of strong acid catalyst, it forms an ester.

Chemistry: The Molecular Nature of Matter and Change - Standalone book, Chapter 15, Problem 15.69P , additional homework tip 3

The condensed formula is a way of representing an organic compound formula in a single line without the vertical bonds.  In condensed formula each carbon atom is grouped with its hydrogens, but all bonds are not shown.

Expert Solution & Answer
Check Mark

Want to see the full answer?

Check out a sample textbook solution
Blurred answer
Previous
Chapter 15, Problem 15.68P
Next
Chapter 15, Problem 15.70P

Chapter 15 Solutions

Chemistry: The Molecular Nature of Matter and Change - Standalone book

Ch. 15.2 - Prob. 15.1AFPCh. 15.2 - Prob. 15.1BFPCh. 15.2 - Prob. 15.2AFPCh. 15.2 - Prob. 15.2BFPCh. 15.2 - How many peaks appear in the NMR spectrum of each...Ch. 15.2 - Prob. B15.2PCh. 15.2 - Prob. B15.3PCh. 15.3 - Prob. 15.3AFPCh. 15.3 - Prob. 15.3BFPCh. 15.4 - Prob. 15.4AFP
Ch. 15.4 - Prob. 15.4BFPCh. 15.4 - Prob. 15.5AFPCh. 15.4 - Prob. 15.5BFPCh. 15.4 - Prob. 15.6AFPCh. 15.4 - Prob. 15.6BFPCh. 15.4 - Prob. 15.7AFPCh. 15.4 - Prob. 15.7BFPCh. 15.6 - Prob. B15.4PCh. 15.6 - Prob. B15.5PCh. 15 - Prob. 15.1PCh. 15 - Prob. 15.2PCh. 15 - Prob. 15.3PCh. 15 - Silicon lies just below carbon in Group 4A(14) and...Ch. 15 - What is the range of oxidation states for carbon?...Ch. 15 - Prob. 15.6PCh. 15 - Prob. 15.7PCh. 15 - Define each type of isomer: (a) constitutional;...Ch. 15 - Prob. 15.9PCh. 15 - Prob. 15.10PCh. 15 - Prob. 15.11PCh. 15 - How does an aromatic hydrocarbon differ from a...Ch. 15 - Prob. 15.13PCh. 15 - Prob. 15.14PCh. 15 - Prob. 15.15PCh. 15 - Prob. 15.16PCh. 15 - Prob. 15.17PCh. 15 - Prob. 15.18PCh. 15 - Prob. 15.19PCh. 15 - Prob. 15.20PCh. 15 - Prob. 15.21PCh. 15 - Prob. 15.22PCh. 15 - Prob. 15.23PCh. 15 - Prob. 15.24PCh. 15 - Draw structures from the following names, and...Ch. 15 - Prob. 15.26PCh. 15 - Prob. 15.27PCh. 15 - Prob. 15.28PCh. 15 - Prob. 15.29PCh. 15 - Prob. 15.30PCh. 15 - Prob. 15.31PCh. 15 - Prob. 15.32PCh. 15 - Prob. 15.33PCh. 15 - Prob. 15.34PCh. 15 - Prob. 15.35PCh. 15 - Prob. 15.36PCh. 15 - Prob. 15.37PCh. 15 - Prob. 15.38PCh. 15 - Prob. 15.39PCh. 15 - Prob. 15.40PCh. 15 - Determine the type of each of the following...Ch. 15 - Prob. 15.42PCh. 15 - Prob. 15.43PCh. 15 - Prob. 15.44PCh. 15 - Prob. 15.45PCh. 15 - Prob. 15.46PCh. 15 - Prob. 15.47PCh. 15 - Prob. 15.48PCh. 15 - Prob. 15.49PCh. 15 - Prob. 15.50PCh. 15 - Prob. 15.51PCh. 15 - Prob. 15.52PCh. 15 - Prob. 15.53PCh. 15 - Prob. 15.54PCh. 15 - Prob. 15.55PCh. 15 - Prob. 15.56PCh. 15 - Prob. 15.57PCh. 15 - Prob. 15.58PCh. 15 - Prob. 15.59PCh. 15 - Prob. 15.60PCh. 15 - Prob. 15.61PCh. 15 - Prob. 15.62PCh. 15 - Prob. 15.63PCh. 15 - Prob. 15.64PCh. 15 - Prob. 15.65PCh. 15 - Prob. 15.66PCh. 15 - Prob. 15.67PCh. 15 - Prob. 15.68PCh. 15 - Prob. 15.69PCh. 15 - Prob. 15.70PCh. 15 - Prob. 15.71PCh. 15 - Prob. 15.72PCh. 15 - Prob. 15.73PCh. 15 - Prob. 15.74PCh. 15 - Prob. 15.75PCh. 15 - Prob. 15.76PCh. 15 - Prob. 15.77PCh. 15 - Prob. 15.78PCh. 15 - Prob. 15.79PCh. 15 - Prob. 15.80PCh. 15 - Prob. 15.81PCh. 15 - Prob. 15.82PCh. 15 - Prob. 15.83PCh. 15 - Prob. 15.84PCh. 15 - Prob. 15.85PCh. 15 - Prob. 15.86PCh. 15 - Prob. 15.87PCh. 15 - What is the key structural difference between...Ch. 15 - Protein shape, function, and amino acid sequence...Ch. 15 - What linkage joins the monomers in each strand of...Ch. 15 - What is base pairing? How does it pertain to DNA...Ch. 15 - RNA base sequence, protein amino acid sequence,...Ch. 15 - Prob. 15.93PCh. 15 - Prob. 15.94PCh. 15 - Draw the structure of each of the following...Ch. 15 - Prob. 15.96PCh. 15 - Write the sequence of the complementary DNA strand...Ch. 15 - Prob. 15.98PCh. 15 - Prob. 15.99PCh. 15 - Prob. 15.100PCh. 15 - Prob. 15.101PCh. 15 - Amino acids have an average molar mass of 100...Ch. 15 - Prob. 15.103PCh. 15 - Prob. 15.104PCh. 15 - Some of the most useful compounds for organic...Ch. 15 - Prob. 15.106PCh. 15 - Prob. 15.107PCh. 15 - Prob. 15.108PCh. 15 - Prob. 15.109PCh. 15 - Prob. 15.110PCh. 15 - Prob. 15.111PCh. 15 - Prob. 15.112PCh. 15 - The polypeptide chain in proteins does not exhibit...Ch. 15 - Prob. 15.114PCh. 15 - Prob. 15.115PCh. 15 - Prob. 15.116PCh. 15 - Prob. 15.117PCh. 15 - Wastewater from a cheese factory has the following...Ch. 15 - Prob. 15.119P
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.
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY
SEE MORE TEXTBOOKS