Essential Organic Chemistry (3rd Edition)
Essential Organic Chemistry (3rd Edition)
3rd Edition
ISBN: 9780321937711
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 6, Problem 48P

(a)

Interpretation Introduction

Interpretation:

The given systematic names should be checked and have to be corrected if the name is wrong.

Concept Introduction:

NOMENCLATURE RULES:

  • The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the functional group which is used as main suffix.
  • Other functional group, if any, should be identified and name it as prefix.
  • Numbering should be done in such a way as to get the lowest number for suffix functional group, multiple bonds.
  • The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
  • If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
  • Select the longest chain which contains the triple bond in such a way to get lowest value for the functional group.
  • Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
  • When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.

Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.

Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.

(b)

Interpretation Introduction

Interpretation:

The given systematic names should be checked and have to be corrected if the name is wrong.

Concept Introduction:

NOMENCLATURE RULES:

  • The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the functional group which is used as main suffix.
  • Other functional group, if any, should be identified and name it as prefix.
  • Numbering should be done in such a way as to get the lowest number for suffix functional group, multiple bonds.
  • The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
  • If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
  • Select the longest chain which contains the triple bond in such a way to get lowest value for the functional group.
  • Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
  • When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.

Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.

Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.

(c)

Interpretation Introduction

Interpretation:

The given systematic names should be checked and have to be corrected if the name is wrong.

Concept Introduction:

NOMENCLATURE RULES:

  • The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the functional group which is used as main suffix.
  • Other functional group, if any, should be identified and name it as prefix.
  • Numbering should be done in such a way as to get the lowest number for suffix functional group, multiple bonds.
  • The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
  • If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
  • Select the longest chain which contains the triple bond in such a way to get lowest value for the functional group.
  • Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
  • When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.

Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.

Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.

(d)

Interpretation Introduction

Interpretation:

The given systematic names should be checked and have to be corrected if the name is wrong.

Concept Introduction:

NOMENCLATURE RULES:

  • The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the functional group which is used as main suffix.
  • Other functional group, if any, should be identified and name it as prefix.
  • Numbering should be done in such a way as to get the lowest number for suffix functional group, multiple bonds.
  • The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
  • If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
  • Select the longest chain which contains the triple bond in such a way to get lowest value for the functional group.
  • Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
  • When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.

Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains , rings or any other hetero atom other than carbon or hydrogen.

Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.

(e)

Interpretation Introduction

Interpretation:

The given systematic names should be checked and have to be corrected if the name is wrong.

Concept Introduction:

NOMENCLATURE RULES:

  • The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the functional group which is used as main suffix.
  • Other functional group, if any, should be identified and name it as prefix.
  • Numbering should be done in such a way as to get the lowest number for suffix functional group, multiple bonds.
  • The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
  • If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
  • Select the longest chain which contains the triple bond in such a way to get lowest value for the functional group.
  • Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
  • When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.

Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains , rings or any other hetero atom other than carbon or hydrogen.

Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.

(f)

Interpretation Introduction

Interpretation:

The given systematic names should be checked and have to be corrected if the name is wrong.

Concept Introduction:

NOMENCLATURE RULES:

  • The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the functional group which is used as main suffix.
  • Other functional group, if any, should be identified and name it as prefix.
  • Numbering should be done in such a way as to get the lowest number for suffix functional group, multiple bonds.
  • The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
  • If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
  • Select the longest chain which contains the triple bond in such a way to get lowest value for the functional group.
  • Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
  • When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.

Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.

Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.

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Please do the following question. Step by step . A. 1-methyl-1,3-cyclohexadiene + HBr B. 2-methyl-1,3-pentadiene + 1,4-cyclohexadiene
Determine the number of carbons present in the compound based on the base name. Draw the carbon chain and include any double or triple bonds if indicated in the suffix of the base name. Number each carbon. The carbons can be numbered from left to right or right to left. Draw any substituents on the corresponding carbon atom for which is indicated in the name. Refer to Figures 4 and 5 in the background for a visual representation of numbered carbons with corresponding substituents. Check that each carbon atom has a total of 4 bonds.
Finish the indicated reaction by filling in and starting materials, reagents or products as needed 

Chapter 6 Solutions

Essential Organic Chemistry (3rd Edition)

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