Solveeit Logo
Login

Question

Question: The IUPAC name of compound \(C{{H}_{2}}=CH-CH{{\left( C{{H}_{3}} \right)}_{2}}\) is: A) 1, 1-dimet...

The IUPAC name of compound CH2=CH−CH(CH3)2C{{H}_{2}}=CH-CH{{\left( C{{H}_{3}} \right)}_{2}} is:
A) 1, 1-dimethyl-2-propane
B) 2-vinyl propene
C) 3-methyl-1-butene
D) 2-vinyl propane

Explanation

Solution

In IUPAC naming system, unsaturated hydrocarbons are named in such a way that the parent chain containing multiple bonds has the lowest number.

Complete step by step answer:
CH2=CH−CH(CH3)C{{H}_{2}}=CH-CH\left( C{{H}_{3}} \right)is an alkene molecule.
First of all we need to understand what IUPAC nomenclature is. In chemical nomenclature, IUPAC nomenclature of organic chemistry is a method of naming organic compounds as recommended by the International Union of Pure and Applied Chemistry.
One needs to follow certain rules while naming alkenes in IUPAC naming system.
1. The parent chain chosen is the longest chain that must include both carbon atoms of the double bond.
2. The root chain must be numbered from the end nearest a double bond carbon atom. If the double bond is in the center of the chain, the nearest substituent rule is used to determine the end where numbering starts.
3. Double bonds in hydrocarbon are indicated by replacing the suffix – ane with ene.
4. If more than one double bond is present the compound is named as a diene, triene or equivalent prefix indicating the number of double bonds, and each double bond is assigned a locator number.
Considering the following information we can now name the organic compound.
Considering the parent chain and numbering the organic molecule

Thus, the name of the organic compound is 3-methyl-1-butene. Hence, option C is correct.

Note:
A student might write 3-methyl-1-butene as 3-methyl-but-1-ene as well. Both are correct. Also, students must be very careful while naming unsaturated hydrocarbons containing both double and triple bonds. While assigning priority, double bonds are given more priority than triple bonds. The location of double bond is indicated before the parent name while the location of the triple bond is indicated between the -en and –yne suffixes (notice that the e is left off, -en is used instead of -ene).
For example,
is named as pent-1-en-4-yne.