Concept explainers
a) 2-Methyl-1, 5-hexadiene
Interpretation:
The structure corresponding to the IUPAC name 2-Methyl-1, 5-hexadiene is to be drawn.
Concept introduction:
The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound – the
To draw:
The structure corresponding to the IUPAC name 2-Methyl-1, 5-hexadiene.
b) 3-Ethyl-2, 2-dimethyl-3-heptene
Interpretation:
The structure corresponding to the IUPAC name 3-Ethyl-2, 2-dimethyl-3-heptene is to be drawn.
Concept introduction:
The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound – the alkene name ends with the suffix –ene. The chain is to be numbered from the end that gives the lowest number to the carbon in double bond. Substituents are to be numbered according to their positions in the chain and listed alphabetically. The position of the double bond is indicated by giving the number of the first alkene carbon before the name of the parent name. If more than one double bond is present, their positions are indicated with the suffixes -diene, -triene and so on.
To draw:
The structure corresponding to the IUPAC name 3-Ethyl-2, 2-dimethyl-3-heptene.
c) 2, 3, 3-trimethyl-1, 4, 6-octatriene
Interpretation:
The structure corresponding to the IUPAC name 2, 3, 3-trimethyl-1, 4, 6-octatriene is to be drawn.
Concept introduction:
The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound – the alkene name ends with the suffix –ene. The chain is to be numbered from the end that gives the lowest number to the carbon in double bond. Substituents are to be numbered according to their positions in the chain and listed alphabetically. The position of the double bond is indicated by giving the number of the first alkene carbon before the name of the parent name. If more than one double bond is present, their positions are indicated with the suffixes -diene, -triene and so on.
To draw:
The structure corresponding to the IUPAC name 2, 3, 3-trimethyl-1, 4, 6-octatriene.
d) 3, 4-Diisopropyl-2, 5-dimethyl-3-hexene
Interpretation:
The structure corresponding to the IUPAC name 3, 4-diisopropyl-2, 5-dimethyl-3-hexene is to be drawn.
Concept introduction:
The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound – the alkene name ends with the suffix –ene. The chain is to be numbered from the end that gives the lowest number to the carbon in double bond. Substituents are to be numbered according to their positions in the chain and listed alphabetically. The position of the double bond is indicated by giving the number of the first alkene carbon before the name of the parent name. If more than one double bond is present, their positions are indicated with the suffixes -diene, -triene and so on.
To draw:
The structure corresponding to the IUPAC name 3, 4-diisopropyl-2, 5-dimethyl-3-hexene.
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Chapter 7 Solutions
Organic Chemistry
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- Draw line structures for the following alkenes. Which can exist as cis–trans isomers? For those that can, draw both isomers.(a) 2-Methyloct-2-ene (b) Hept-3-ene(c) 3,4-Dimethylhex-3-enearrow_forwardDraw the structure of (a) 4-isopropylheptane (b) 1,1-dichlorocyclopentane (c) cis-3-octenearrow_forwardDraw the structures corresponding to the following names(a) 2-chloro-3,3-dimethylhexane (b) 3,3-dichloro-2-methylhexane( c) 3-bromo-3-ethylpentane(d) 2-bromo-5-chloro-3-methylhexanearrow_forward
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