Essential Organic Chemistry, Global Edition
Essential Organic Chemistry, Global Edition
3rd Edition
ISBN: 9781292089034
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 3, Problem 55P

(a)

Interpretation Introduction

Interpretation:

The systematic name for each isomer has to be given.

Concept introduction:

The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).  IUPAC name consists of three parts in major namely Prefix, suffix and root word.

The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments.  For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon.  For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment. 

Prefix: Represents the substituent present in the molecule and its position in the root name.

Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.  For example alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.

(b)

Interpretation Introduction

Interpretation:

The common name for each isomer has to be given.

Concept introduction:

The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).IUPAC name consists of three parts in major namely Prefix, suffix and root word.

The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments.  For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon.  For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment. 

Prefix: Represents the substituent present in the molecule and its position in the root name.

Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.  For example alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.

(c)

Interpretation Introduction

Interpretation:

The number of primary alkyl halides has to be given.

Concept introduction:

The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).IUPAC name consists of three parts in major namely Prefix, suffix and root word.

The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments.  For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon.  For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment. 

Prefix: Represents the substituent present in the molecule and its position in the root name.

Suffix: Denotes the presence of functional group if any in the molecule.  It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.  For example alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.

(d)

Interpretation Introduction

Interpretation:

The number of secondary alkyl halide has to be given.

Concept introduction:

The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).  IUPAC name consists of three parts in major namely Prefix, suffix and root word.

The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments.  For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon.  For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment. 

Prefix: Represents the substituent present in the molecule and its position in the root name.

Suffix: Denotes the presence of functional group if any in the molecule.  It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.  For example alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.

(e)

Interpretation Introduction

Interpretation:

The number of tertiary alkyl halide has to be given.

Concept introduction:

The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).  IUPAC name consists of three parts in major namely Prefix, suffix and root word.

The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments.  For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon.  For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.

Prefix: Represents the substituent present in the molecule and its position in the root name.

Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.  For example alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Nomenclature of organic molecules: The particular functional group connected into a primary carbon atom, while secondary and tertiary groups in (C2 and C3) place of carbon atoms it is called primary, secondary and tertiary structures.

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Chapter 3 Solutions

Essential Organic Chemistry, Global Edition

Ch. 3.3 - Draw a condensed and a skeletal structure for the...Ch. 3.3 - What is each compounds systematic name?Ch. 3.4 - Prob. 17PCh. 3.4 - Give two names for each of the following alkyl...Ch. 3.5 - Are the following compounds primary, secondary, or...Ch. 3.5 - Name the following amines and tell whether they...Ch. 3.5 - Draw the structures and provide systematic names...Ch. 3.6 - Predict the approximate size of the following bond...Ch. 3.7 - What is the smallest straight-chain alkane that is...Ch. 3.7 - Prob. 24PCh. 3.7 - Prob. 25PCh. 3.7 - Prob. 26PCh. 3.7 - List the compounds in each set from highest...Ch. 3.8 - Rank the following compounds in each set from most...Ch. 3.8 - In which solvent would cyclohexane have the lowest...Ch. 3.8 - Prob. 30PCh. 3.9 - Prob. 31PCh. 3.9 - a. Draw the three staggered conformations and the...Ch. 3.9 - a. Draw the most stable conformation of pentane...Ch. 3.11 - Draw 1,2,3,4,5,6-hexachlorocyclohexane with a. all...Ch. 3.12 - At any one time, would you expect there to be more...Ch. 3.13 - Prob. 36PCh. 3 - a. How many hydrogens does an alkane with 17...Ch. 3 - Prob. 2PCh. 3 - Draw a condensed structure and a skeletal...Ch. 3 - Prob. 39PCh. 3 - Prob. 40PCh. 3 - Which of the following represents a cis isomer?Ch. 3 - a. How many primary carbons does each of the...Ch. 3 - Name the following amines and tell whether they...Ch. 3 - Which of the following conformers of isobutyl...Ch. 3 - What is each compounds name? a. CH3CH2CH2OCH2CH3Ch. 3 - Draw the structural formula for an alkane that has...Ch. 3 - Which has a. the higher boiling point:...Ch. 3 - Ansaid and Motrin belong to the group of drugs...Ch. 3 - A student was given the structural formulas of...Ch. 3 - Which of the following conformers has the highest...Ch. 3 - Prob. 51PCh. 3 - Draw skeletal structures for the following: a....Ch. 3 - Prob. 53PCh. 3 - For rotation about the C-3 8 C-4 bond of...Ch. 3 - Prob. 55PCh. 3 - What is each compounds systematic name?Ch. 3 - Draw the two chair conformers for each of the...Ch. 3 - Draw the nine constitutional isomers with...Ch. 3 - Prob. 59PCh. 3 - Prob. 60PCh. 3 - Prob. 61PCh. 3 - Using Newman projections, draw the most stable...Ch. 3 - For each of the following disubstituted...Ch. 3 - Prob. 64PCh. 3 - Prob. 65PCh. 3 - What is each compounds systematic name?Ch. 3 - Prob. 67PCh. 3 - Bromine is a larger atom than chlorine, but the...Ch. 3 - Prob. 69PCh. 3 - Prob. 70PCh. 3 - a. Draw a potential energy diagram for rotation...
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