INTRODUCTION TO CHEMISTRY-ACCESS
INTRODUCTION TO CHEMISTRY-ACCESS
5th Edition
ISBN: 9781260518542
Author: BAUER
Publisher: MCG
bartleby

Concept explainers

Question
Book Icon
Chapter 16, Problem 1QP

(a)

Interpretation Introduction

Interpretation:

The given statement, “a compound having the same composition and formula as another compound, but a different structure�, is to be matched to its appropriate key term.

(a)

Expert Solution
Check Mark

Explanation of Solution

The isomers of a compound have the same molecular formula with a different arrangement of atoms. Thus, the term, ‘isomer’, refers to a compound with the same composition and formula as another compound, but a different structure.

(b)

Interpretation Introduction

Interpretation:

The given statement, “an organic compound containing the functional group, OH �, is to be matched to its appropriate key term.

(b)

Expert Solution
Check Mark

Explanation of Solution

Alcohols are characterized by the presence of the functional group, OH . Thus, the term, ‘alcohol’, refers to an organic compound containing the functional group, OH .

(c)

Interpretation Introduction

Interpretation:

The given statement, “a condensation product of carboxylic acids and alcohols having the general formula, RCO2R' �, is to be matched to its appropriate key term.

(c)

Expert Solution
Check Mark

Explanation of Solution

Esters are formed by the condensation of carboxylic acids with alcohol.

RCOOH+R'OHRCOOR'+H2O

Thus, the term, ‘ester’, corresponds to a condensation product of carboxylic acids and alcohols having the general formula, RCO2R' .

(d)

Interpretation Introduction

Interpretation:

The given statement, “an organic compound containing the functional group, CHO �, is to be matched to its appropriate key term.

(d)

Expert Solution
Check Mark

Explanation of Solution

In aldehydes, the carbonyl group is bonded to a hydrogen atom. Thus, the term, ‘aldehyde’, corresponds to an organic compound containing the CHO functional group.

(e)

Interpretation Introduction

Interpretation:

The given statement, ‘a hydrocarbon that has a ring or closed chain structure�, is to be matched to its appropriate key term.

(e)

Expert Solution
Check Mark

Explanation of Solution

Cyclic hydrocarbons contain a closed chain of carbon atoms. Thus, the term, ‘cyclic hydrocarbon’, corresponds to a hydrocarbon that has a ring or closed chain structure.

(f)

Interpretation Introduction

Interpretation:

The given statement, “a hydrocarbon that contains all the hydrogens it can hold as a result of having only carbon-carbon single bonds�, is to be matched to its appropriate key term.

(f)

Expert Solution
Check Mark

Explanation of Solution

In a saturated hydrocarbon, the carbon atom forms four bonds. In alkanes, the bonds between carbon atoms are single bonds. So, each carbon atom is attached to the highest possible number of hydrogen atoms. Thus, the term, ‘saturated hydrocarbon’, corresponds a hydrocarbon that contains all the hydrogens it can hold as a result of having only carbon-carbon single bonds.

(g)

Interpretation Introduction

Interpretation:

The given statement, “a group derived from an alkane by the removal of a hydrogen atom�, is to be matched to its appropriate key term.

(g)

Expert Solution
Check Mark

Explanation of Solution

When a hydrogen atom is removed from an alkane, the group obtained is called an alkyl group. Thus, the term, ‘alkyl group’, corresponds to a group derived from an alkane.

(h)

Interpretation Introduction

Interpretation:

The given statement, “a saturated hydrocarbon that contains a ring structure�, is to be matched to its appropriate key term.

(h)

Expert Solution
Check Mark

Explanation of Solution

In a saturated hydrocarbon, all the carbon-carbon bonds are single. They are also called alkanes. Alkanes can be closed ring or open chained. A closed ring of carbon atoms containing all single bonds is called a cycloalkane. Thus, the term, ‘cycloalkane’, corresponds to a saturated hydrocarbon that contains a ring structure.

(i)

Interpretation Introduction

Interpretation:

The given statement, “a hydrocarbon that contains localized single, double or triple bonds�, is to be matched to its appropriate key term.

(i)

Expert Solution
Check Mark

Explanation of Solution

In aliphatic hydrocarbons, the electrons in the bonds are not delocalized and there is no resonance. However, the bonds between carbon atoms can be single, double or triple. Thus, the term, ‘aliphatic hydrocarbon’, corresponds to a hydrocarbon that contains localized single, double or triple bonds.

(j)

Interpretation Introduction

Interpretation:

The given statement, “a small molecule that contains both, the NH2 and CO2H functional groups�, is to be matched to its appropriate key term.

(j)

Expert Solution
Check Mark

Explanation of Solution

Amino acids contain both amino and carboxylic acid groups. Glycine is the smallest amino acid that contains both, the NH2 and CO2H functional groups. Thus, the term, ‘amino acids’, correspond to the molecules containing both, the NH2 and CO2H functional groups.

(k)

Interpretation Introduction

Interpretation:

The given statement, “the study of organic compounds�, is to be matched to its appropriate key term.

(k)

Expert Solution
Check Mark

Explanation of Solution

Organic compounds are compounds made of carbon. The subject that deals with the study of organic compounds is called organic chemistry. Thus, the term, ‘organic chemistry’, refers to the study of organic compounds.

(l)

Interpretation Introduction

Interpretation:

The given statement, “a hydrocarbon that does not contain all the hydrogen atoms that could possibly be included due to multiple carbon-carbon bonds�, is to be matched to its appropriate key term.

(l)

Expert Solution
Check Mark

Explanation of Solution

An unsaturated hydrocarbon contains multiple bonds between the carbon atoms. So, the carbon atom is attached to a smaller number of hydrogen atoms as a carbon atom can form only four bonds with other atoms. Thus, the term, ‘unsaturated hydrocarbon’, corresponds to the hydrocarbons that do not contain all the hydrogen atoms that could possibly be included due to multiple carbon-carbon bonds.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
Glucose, C6H12O6, contains an aldehyde group but exist predominantly in the form of the cyclic hemiacetal show below.   A cyclic hemiacetal is formed when the —OH group of one carbon bonds to the carbonyl group of another carbon.  Identify which carbon provides the —OH group and which provides the —CHO?  Give a functional isomer of glucose and draw its structure.
draw the structure of C8H10NO7P2-  and give the general name of the functional group
1a. . Isomers are responsible for the diversity of organic compounds. true or false?  b. Positional isomers are molecules with different arrangements of the carbon skeleton but with the same chemical formula.  true or false?  c.)

Chapter 16 Solutions

INTRODUCTION TO CHEMISTRY-ACCESS

Ch. 16 - Prob. 2PPCh. 16 - Prob. 3PPCh. 16 - Prob. 4PPCh. 16 - Prob. 5PPCh. 16 - Prob. 6PPCh. 16 - Prob. 7PPCh. 16 - Prob. 8PPCh. 16 - Prob. 9PPCh. 16 - Prob. 10PPCh. 16 - Prob. 11PPCh. 16 - Prob. 1QPCh. 16 - Prob. 2QPCh. 16 - Prob. 3QPCh. 16 - Prob. 4QPCh. 16 - Prob. 5QPCh. 16 - Prob. 6QPCh. 16 - Prob. 7QPCh. 16 - Prob. 8QPCh. 16 - Prob. 9QPCh. 16 - Prob. 10QPCh. 16 - Prob. 11QPCh. 16 - Prob. 12QPCh. 16 - Prob. 13QPCh. 16 - Prob. 14QPCh. 16 - Prob. 15QPCh. 16 - Prob. 16QPCh. 16 - Prob. 17QPCh. 16 - Prob. 18QPCh. 16 - Prob. 19QPCh. 16 - Prob. 20QPCh. 16 - Prob. 21QPCh. 16 - Prob. 22QPCh. 16 - Prob. 23QPCh. 16 - Prob. 24QPCh. 16 - Prob. 25QPCh. 16 - Prob. 26QPCh. 16 - Prob. 27QPCh. 16 - Prob. 28QPCh. 16 - Prob. 29QPCh. 16 - Prob. 30QPCh. 16 - Prob. 31QPCh. 16 - Prob. 32QPCh. 16 - Prob. 33QPCh. 16 - Prob. 34QPCh. 16 - Prob. 35QPCh. 16 - Prob. 36QPCh. 16 - Prob. 37QPCh. 16 - Prob. 38QPCh. 16 - Prob. 39QPCh. 16 - Prob. 40QPCh. 16 - Prob. 41QPCh. 16 - Write IUPAC names for the following compounds....Ch. 16 - Prob. 43QPCh. 16 - Prob. 44QPCh. 16 - Prob. 45QPCh. 16 - Prob. 46QPCh. 16 - Prob. 47QPCh. 16 - Prob. 48QPCh. 16 - Prob. 49QPCh. 16 - Prob. 50QPCh. 16 - Prob. 51QPCh. 16 - Prob. 52QPCh. 16 - Prob. 53QPCh. 16 - Prob. 54QPCh. 16 - Prob. 55QPCh. 16 - Prob. 56QPCh. 16 - Prob. 57QPCh. 16 - Prob. 58QPCh. 16 - Prob. 59QPCh. 16 - Prob. 60QPCh. 16 - Prob. 61QPCh. 16 - Prob. 62QPCh. 16 - Prob. 63QPCh. 16 - Prob. 64QPCh. 16 - Prob. 65QPCh. 16 - Prob. 66QPCh. 16 - Prob. 67QPCh. 16 - Prob. 68QPCh. 16 - Prob. 69QPCh. 16 - Prob. 70QPCh. 16 - Prob. 71QPCh. 16 - Prob. 72QPCh. 16 - Prob. 73QPCh. 16 - Prob. 74QPCh. 16 - Prob. 75QPCh. 16 - Prob. 76QPCh. 16 - Prob. 77QPCh. 16 - Prob. 78QPCh. 16 - Prob. 79QPCh. 16 - Prob. 80QPCh. 16 - Prob. 81QPCh. 16 - Prob. 82QPCh. 16 - Prob. 83QPCh. 16 - Prob. 84QPCh. 16 - Prob. 85QPCh. 16 - Prob. 86QPCh. 16 - Prob. 87QPCh. 16 - Prob. 88QPCh. 16 - Predict and explain the relative boiling points of...Ch. 16 - Prob. 90QPCh. 16 - Prob. 91QPCh. 16 - Prob. 92QPCh. 16 - Prob. 93QPCh. 16 - Prob. 94QPCh. 16 - Prob. 95QPCh. 16 - Prob. 96QPCh. 16 - Prob. 97QPCh. 16 - Prob. 98QPCh. 16 - Prob. 99QPCh. 16 - Prob. 100QPCh. 16 - Prob. 101QPCh. 16 - Prob. 102QPCh. 16 - Prob. 103QPCh. 16 - Prob. 104QPCh. 16 - Prob. 105QPCh. 16 - Prob. 106QPCh. 16 - Prob. 107QPCh. 16 - Prob. 108QPCh. 16 - Prob. 109QPCh. 16 - Prob. 110QPCh. 16 - Prob. 111QPCh. 16 - Prob. 112QPCh. 16 - Prob. 113QPCh. 16 - Prob. 114QPCh. 16 - Prob. 115QPCh. 16 - Prob. 116QPCh. 16 - Prob. 117QPCh. 16 - Prob. 118QPCh. 16 - Prob. 119QPCh. 16 - Prob. 120QPCh. 16 - Prob. 121QPCh. 16 - Draw the line structures for the ether and two...Ch. 16 - Prob. 123QPCh. 16 - Prob. 124QPCh. 16 - Prob. 125QPCh. 16 - Prob. 126QPCh. 16 - Write structural formulas for all the isomers of...Ch. 16 - Prob. 128QPCh. 16 - Prob. 129QPCh. 16 - Prob. 130QPCh. 16 - Prob. 131QPCh. 16 - Prob. 132QPCh. 16 - Prob. 133QPCh. 16 - Prob. 134QPCh. 16 - Prob. 135QPCh. 16 - Prob. 136QPCh. 16 - Prob. 137QPCh. 16 - Prob. 138QPCh. 16 - Prob. 139QPCh. 16 - Prob. 140QPCh. 16 - Prob. 141QPCh. 16 - Prob. 142QPCh. 16 - Prob. 143QP
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
Introductory Chemistry For Today
Chemistry
ISBN:9781285644561
Author:Seager
Publisher:Cengage
Text book image
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Text book image
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning