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 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 use either full structural diagrams or the combination method shown in the lesson. Skeletal/line diagrams will not be accepted. a. 5-butyl-4-ethyl-6- methylhept-3 - ene b. 3-propyl-2-methylcyclohept-1 - ene c. 2, 5, 5, 6-tetramethylhept-3-yne d. 1-ethyl-3- propylbenzene
A student was given the structural formulas of several compounds and was asked to give them systematic names. How many did the student name correctly? Correct those that are misnamed. a. 4-bromo-3-pentanol b. 2,2-dimethyl-4-ethylheptane c. 5-methylcyclohexanol d. 1,1-dimethyl-2-cyclohexanol e. 5-(2,2-dimethylethyl)nonane f. isopentylbromide g. 3,3-dichlorooctane h. 5-ethyl-2-methylhexane i. 1-bromo-4-pentanol   j. 3-isopropyloctane  k. 2-methyl-2-isopropylheptane  l. 2-methyl-N,N-dimethyl-4-hexanamine

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Essential Organic Chemistry, Global Edition

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