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Chapter 1: Problem 132

The IUPAC name of \(\quad 1\) is CCC(C)CC(CC)CC (a) 5 -heptenylheptane (b) 3 -heptylhept-3-ene (c) 3 -(3-heptyl) hept-3-ene (d) 5,6-Diethyl-3-methyldec-4-ene

Short Answer

Expert verified
Answer: The correct IUPAC name for the compound is 3-ethyl-6-propylhept-3-ene.

Step by step solution

01

Count the carbon atoms of the longest chain

For the given compound, we need to find the longest continuous chain of carbon atoms. The SMILES notation is "CCC(C)CC(CC)CC", which translates to a structure with a chain of 5 carbon atoms with two branches.
02

Identify the functional groups and find their position

After identifying the longest carbon chain, we should now look for any functional groups present in the compound. In this case, there is an alkene functional group, which is a carbon-carbon double bond. The double bond is present between the 3rd and 4th carbon atoms, making the compound an alkene.
03

Locate and name the substituents

Now we need to find and name the substituents on the longest chain. There are two substituents: an ethyl group (C2H5) on the 3rd carbon atom and a propyl group (C3H7) on the 6th carbon atom.
04

Name the compound using IUPAC rules

Following IUPAC rules, we can name this compound by combining the information from steps 1-3. Firstly, name the longest chain with the appropriate alkene suffix (i.e., "hept-3-ene"). Secondly, include the substituent names along with their position in the chain, separated by hyphens. The compound can be named as 3-ethyl-6-propylhept-3-ene.
05

Compare the correct IUPAC name with the options provided

Now that we have determined the correct IUPAC name for the compound, we can compare it with the given options: (a) 5-heptenylheptane (b) 3-heptylhept-3-ene (c) 3-(3-heptyl)hept-3-ene (d) 5,6-Diethyl-3-methyldec-4-ene None of the provided options match the correct IUPAC name, indicating an error or inconsistency in this exercise.

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Most popular questions from this chapter

The least stable cabocation among the following is (a) \(\mathrm{CH}_{3}-\mathrm{CH}_{2}^{+}\) (b) \(\mathrm{F}_{3} \mathrm{C}-\mathrm{CH}_{2}\) (c) \(\mathrm{F}_{3} \mathrm{C}\) (d) \(\mathrm{CH}_{3}-\mathrm{CH}=\stackrel{+}{\mathrm{C}} \mathrm{H}\)

Which of the following pairs are isostructural? (a) \({\mathrm{C}} \mathrm{C}_{3}\) and \(\mathrm{CH}_{3}^{-}\) (b) \(\ddot{\mathrm{N} H}_{3}\) and \(\mathrm{CH}_{3}^{-}\) (c) \(\ddot{\mathrm{N} H}_{3}\) and \(\mathrm{CH}_{3}^{-}\) (d) \(\mathrm{BCl}_{3}\) and \(\mathrm{CH}_{3}{ }^{+}\)

A compound with molecular formula \(\mathrm{C}_{7} \mathrm{H}_{16}\) exhibits optical isomerism. The compound is (a) 2,5 dimethylhexane (b) \(2-2\) -dimethylpentane (c) 3 -methylpentane (d) 2,3 -dimethylpentane

Identify the correct statements among the following (I) Removal of a proton from \(\left(\mathrm{H}_{3} \mathrm{C}\right)_{2} \mathrm{CH}-\mathrm{CH}-\mathrm{CH}_{3}\) leads to a more stable carbocation. (II) The hydrogen bonding is strong in \(\mathrm{S}-\mathrm{H}-\mathrm{-} \mathrm{S}\). (III) The central carbon atom in a \(\left(\mathrm{CH}_{3}\right)_{3} \mathrm{C}^{\bullet}\) free radical possesses 5 electrons. (IV) The number of \(\sigma\) bonds in but-1-en-3-yne is 7 . (a) all are correct (b) (IV) only' (c) (I) and (IV) only (d) (I), (III) and (IV)

The number of stereoisomers possible for 2,4 -hexadiene is (a) 4 (b) 2 (c) 3 (d) 6
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