Organic Chemistry: Structure and Function
8th Edition
ISBN: 9781319079451
Author: K. Peter C. Vollhardt, Neil E. Schore
Publisher: W. H. Freeman
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Question
Chapter 6, Problem 32P
(a)
Interpretation Introduction
Interpretation:
The structure of 3-ethyl-2-iodopentane should be drawn.
Concept Introduction:
There are few steps in
- Find the longest carbon chain in the molecule and name it.
- Number the longest carbon chain in such a way that the halogen atoms get the lowest number.
- If there are multiple halogen atoms from same atom, a prefix as di, tri, tetra is added to denote the number of halogen atoms.
- Different types of halogens are named in alphabetical order.
- Position of the halogen atom is indicated by writing the number of carbon atom it is attached before the name of the parent hydrocarbon.
- The name is ended as a normal
alkane .
(b)
Interpretation Introduction
Interpretation:
The structure of 3-bromo-1,1-dichlorobutane should be drawn.
Concept Introduction:
There are few steps in IUPAC nomenclature,
- Find the longest carbon chain in the molecule and name it.
- Number the longest carbon chain in such a way that the halogen atoms get the lowest number.
- If there are multiple halogen atoms from same atom, a prefix as di, tri, tetra is added to denote the number of halogen atoms.
- Different types of halogens are named in alphabetical order.
- Position of the halogen atom is indicated by writing the number of carbon atom it is attached before the name of the parent hydrocarbon.
- The name is ended as a normal alkane.
(c)
Interpretation Introduction
Interpretation:
The structure of cis-1-(bromomethyl)-2-(2-chloroethyl)cyclobutane should be drawn.
Concept Introduction:
There are few steps in IUPAC nomenclature,
- Find the longest carbon chain in the molecule and name it.
- Number the longest carbon chain in such a way that the halogen atoms get the lowest number.
- If there are multiple halogen atoms from same atom, a prefix as di, tri, tetra is added to denote the number of halogen atoms.
- Different types of halogens are named in alphabetical order.
- Position of the halogen atom is indicated by writing the number of carbon atom it is attached before the name of the parent hydrocarbon.
- The name is ended as a normal alkane.
(d)
Interpretation Introduction
Interpretation:
The structure of (trichloromethyl)cyclopropane should be drawn.
Concept Introduction:
There are few steps in IUPAC nomenclature,
- Find the longest carbon chain in the molecule and name it.
- Number the longest carbon chain in such a way that the halogen atoms get the lowest number.
- If there are multiple halogen atoms from same atom, a prefix as di, tri, tetra is added to denote the number of halogen atoms.
- Different types of halogens are named in alphabetical order.
- Position of the halogen atom is indicated by writing the number of carbon atom it is attached before the name of the parent hydrocarbon.
- The name is ended as a normal alkane.
(e)
Interpretation Introduction
Interpretation:
The structure of 1,2,3-trichloro-2-methylpropane should be drawn.
Concept Introduction:
There are few steps in IUPAC nomenclature,
- Find the longest carbon chain in the molecule and name it.
- Number the longest carbon chain in such a way that the halogen atoms get the lowest number.
- If there are multiple halogen atoms from same atom, a prefix as di, tri, tetra is added to denote the number of halogen atoms.
- Different types of halogens are named in alphabetical order.
- Position of the halogen atom is indicated by writing the number of carbon atom it is attached before the name of the parent hydrocarbon.
- The name is ended as a normal alkane.
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Chapter 6 Solutions
Organic Chemistry: Structure and Function
Ch. 6.2 - Prob. 6.1ECh. 6.2 - Prob. 6.3TIYCh. 6.3 - Prob. 6.4ECh. 6.3 - Prob. 6.5ECh. 6.3 - Prob. 6.6ECh. 6.3 - Prob. 6.7ECh. 6.3 - Prob. 6.8ECh. 6.4 - Prob. 6.10TIYCh. 6.4 - Prob. 6.11ECh. 6.5 - Prob. 6.12E
Ch. 6.5 - Prob. 6.13ECh. 6.6 - Prob. 6.14ECh. 6.6 - Prob. 6.16TIYCh. 6.6 - Prob. 6.17ECh. 6.7 - Prob. 6.18ECh. 6.7 - Prob. 6.19ECh. 6.7 - Prob. 6.20ECh. 6.8 - Prob. 6.21ECh. 6.8 - Prob. 6.22ECh. 6.8 - Prob. 6.23ECh. 6.8 - Prob. 6.24ECh. 6.9 - Prob. 6.26TIYCh. 6.10 - Prob. 6.27ECh. 6.10 - Prob. 6.28ECh. 6 - Prob. 31PCh. 6 - Prob. 32PCh. 6 - Prob. 33PCh. 6 - Prob. 34PCh. 6 - Prob. 35PCh. 6 - Prob. 36PCh. 6 - Prob. 37PCh. 6 - Prob. 38PCh. 6 - Prob. 39PCh. 6 - Prob. 40PCh. 6 - Prob. 41PCh. 6 - Prob. 42PCh. 6 - Prob. 43PCh. 6 - Prob. 44PCh. 6 - Prob. 45PCh. 6 - Prob. 46PCh. 6 - Prob. 47PCh. 6 - Prob. 48PCh. 6 - Prob. 49PCh. 6 - Prob. 50PCh. 6 - Prob. 51PCh. 6 - Prob. 52PCh. 6 - Prob. 53PCh. 6 - Prob. 54PCh. 6 - Prob. 55PCh. 6 - Prob. 56PCh. 6 - Prob. 57PCh. 6 - Prob. 58PCh. 6 - Prob. 59PCh. 6 - Prob. 60PCh. 6 - Prob. 61PCh. 6 - Prob. 62PCh. 6 - Prob. 63PCh. 6 - Prob. 64PCh. 6 - Prob. 65PCh. 6 - Prob. 66PCh. 6 - Prob. 67PCh. 6 - Prob. 68P
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