Organic Chemistry - MasteringChemistry
Organic Chemistry - MasteringChemistry
7th Edition
ISBN: 9780321867148
Author: Bruice
Publisher: PEARSON
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Chapter 19, Problem 47P

(a)

Interpretation Introduction

Interpretation:

The given compound has to be named.

Concept Introduction:

IUPAC 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 that 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 contain 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.

(b)

Interpretation Introduction

Interpretation:

The given compound has to be named.

Concept Introduction:

IUPAC 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 that 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 contain 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.

(c)

Interpretation Introduction

Interpretation:

The given compound has to be named.

Concept Introduction:

IUPAC 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 that 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 contain 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.

(d)

Interpretation Introduction

Interpretation:

The given compound has to be named.

Concept Introduction:

IUPAC 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 that 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 contain 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.

(e)

Interpretation Introduction

Interpretation:

The given compound has to be named.

Concept Introduction:

IUPAC 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 that 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 contain 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.

(f)

Interpretation Introduction

Interpretation:

The given compound has to be named.

Concept Introduction:

IUPAC 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 that 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 contain 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.

(g)

Interpretation Introduction

Interpretation:

The given compound has to be named.

Concept Introduction:

IUPAC 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 that 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 contain 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.

(h)

Interpretation Introduction

Interpretation:

The given compound has to be named.

Concept Introduction:

IUPAC 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 that 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 contain 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.

(i)

Interpretation Introduction

Interpretation:

The given compound has to be named.

Concept Introduction:

IUPAC 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 that 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 contain 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.

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Chapter 19 Solutions

Organic Chemistry - MasteringChemistry

Ch. 19.13 - Prob. 13PCh. 19.13 - Prob. 14PCh. 19.14 - Prob. 15PCh. 19.14 - List the compounds in each set from most reactive...Ch. 19.15 - Prob. 18PCh. 19.15 - What product(s) result from nitration of each of...Ch. 19.15 - Prob. 20PCh. 19.16 - Which acid in each of the following pairs is...Ch. 19.16 - Prob. 23PCh. 19.16 - Prob. 24PCh. 19.18 - Show how the following compounds can be...Ch. 19.18 - Give the products, if any, of each of the...Ch. 19.19 - a. Does a coupling reaction have to be used to...Ch. 19.19 - PROBLEM 28 Show how each of the following...Ch. 19.20 - What is the major product(s) of each of the...Ch. 19.20 - Prob. 30PCh. 19.21 - Why isn't FeBr3 used as a catalyst in the first...Ch. 19.21 - Prob. 33PCh. 19.21 - Write the sequence of steps required for the...Ch. 19.21 - Prob. 35PCh. 19.22 - What product is formed from reaction of...Ch. 19.22 - Prob. 37PCh. 19.22 - Draw the structure of the activated ring and the...Ch. 19.23 - Prob. 39PCh. 19.23 - Prob. 40PCh. 19.23 - Diazomethane can be used to convert a carboxylic...Ch. 19.24 - Prob. 42PCh. 19.24 - Prob. 43PCh. 19.24 - Prob. 44PCh. 19.25 - Prob. 45PCh. 19 - Draw the structure for each of the following: a....Ch. 19 - Prob. 47PCh. 19 - Prob. 48PCh. 19 - Prob. 49PCh. 19 - For each of the statements in Column I, choose a...Ch. 19 - What product is obtained from the reaction of...Ch. 19 - Draw the product(s) of each of the following...Ch. 19 - Rank the following substituted anilines from most...Ch. 19 - Prob. 54PCh. 19 - The compound with the 1H NMR spectrum shown below...Ch. 19 - Prob. 56PCh. 19 - Show how the following compounds can be...Ch. 19 - Prob. 58PCh. 19 - Rank each group of compounds from most reactive to...Ch. 19 - Prob. 60PCh. 19 - Describe two ways to prepare anisole from benzene.Ch. 19 - For each of the following components, indicate the...Ch. 19 - Prob. 63PCh. 19 - Prob. 64PCh. 19 - Prob. 65PCh. 19 - Prob. 66PCh. 19 - An aromatic hydrocarbon with a molecular formula...Ch. 19 - The following tertiary alkyl bromides undergo an...Ch. 19 - Show how the following compounds can be...Ch. 19 - Use the four compounds shown below to answer the...Ch. 19 - a. Rank the following esters from most reactive to...Ch. 19 - A mixture of 0.10 mol benzene and 0.10 mol...Ch. 19 - Prob. 73PCh. 19 - Benzene underwent a Friedel-Crafts acylation...Ch. 19 - Prob. 75PCh. 19 - Prob. 76PCh. 19 - Prob. 77PCh. 19 - Friedel-Crafts alkylations can be carried out with...Ch. 19 - Show how the following compounds can be prepared...Ch. 19 - Prob. 80PCh. 19 - Prob. 81PCh. 19 - a. Describe four ways the following reaction can...Ch. 19 - Propose a mechanism for each of the following...Ch. 19 - Prob. 84PCh. 19 - Describe how naphthalene can he prepared from the...Ch. 19 - Prob. 86PCh. 19 - Using resonance contributors for the carbocation...Ch. 19 - Prob. 88PCh. 19 - When heated with chromic acid, compound A forms...Ch. 19 - Prob. 90PCh. 19 - Prob. 91PCh. 19 - What reagents are required to carry out the...Ch. 19 - Show how the following compounds can be prepared...Ch. 19 - An unknown compound reacts with ethyl chloride and...Ch. 19 - How can you distinguish the following compounds...Ch. 19 - P-Fluoronitrobenzene is more reactive toward...Ch. 19 - a. Explain why the following reaction leads to the...Ch. 19 - Describe how mescaline can be synthesized from...Ch. 19 - Propose a mechanism for the following reaction...Ch. 19 - Explain why hydroxide ion catalyzes the reaction...Ch. 19 - Propose a mechanism for each of the following...Ch. 19 - Prob. 102PCh. 19 - Prob. 103PCh. 19 - Describe how 3-methyl-1-phenyl-3-pentanol can he...Ch. 19 - a. How can aspirin be synthesized from benzene? b....Ch. 19 - Prob. 106PCh. 19 - Show how Novocain, a painkiller used frequently by...Ch. 19 - Prob. 108PCh. 19 - Saccharin, an artificial sweetener, is about 300...
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