Alkene and Alkyne IUPAC Naming
The rules for naming alkenes and alkynes are basically the same.
Instead of ending the name of the molecule with -ane, change the ending to -ene for alkenes and -yne for alkynes
The parent chain is the longest carbon chain containing the double or triple bond
You need to indicate the carbon number at which the double or triple bond is located. Depending on which naming system you use, it can look 2 different ways. For example, a 4 carbon molecule with a double bond between the first and second carbons could be named 1-butene in the old system or but-1-ene in the new system.
The parent chain needs to be numbered so that the double or triple bond has the lowest number possible.
The parent chain would be the six-carbon chain containing the double bond. So this molecule is a hexene.
We’ll number from left to right to give the double bond the number 2.
Numbering right to left would give it the number 4.
So, we have 2-hexene or hex-2-ene so far.
Now, we have to name and number the substituent.
The substituent is a methyl group at carbon 3, so it would be named 3-methyl.
Putting that together, we have 3-methyl-2-hexene or 3-methyl-hex-2-ene.
The parent chain is the six-carbon chain containing the triple bond, so we have a hexyne.
We’ll number from left to right to give the triple bond the number 1.
If we number from right to left, the triple bond would have the number 5.
So, we have 1-hexyne or hex-1-yne so far.
Now, we have to name and number the substituent.
The substituent is a methyl group at carbon 3 (carbon 2 isn’t easy to see but it’s at the end of the triple bond), so we would name it 3-methyl.
Putting it all together, we have 3-methyl-1-hexyne or 3-methyl-hex-1-yne.
The rules for naming alkenes and alkynes are basically the same.
Instead of ending the name of the molecule with -ane, change the ending to -ene for alkenes and -yne for alkynes
The parent chain is the longest carbon chain containing the double or triple bond
You need to indicate the carbon number at which the double or triple bond is located. Depending on which naming system you use, it can look 2 different ways. For example, a 4 carbon molecule with a double bond between the first and second carbons could be named 1-butene in the old system or but-1-ene in the new system.
The parent chain needs to be numbered so that the double or triple bond has the lowest number possible.
The parent chain would be the six-carbon chain containing the double bond. So this molecule is a hexene.
We’ll number from left to right to give the double bond the number 2.
Numbering right to left would give it the number 4.
So, we have 2-hexene or hex-2-ene so far.
Now, we have to name and number the substituent.
The substituent is a methyl group at carbon 3, so it would be named 3-methyl.
Putting that together, we have 3-methyl-2-hexene or 3-methyl-hex-2-ene.
The parent chain is the six-carbon chain containing the triple bond, so we have a hexyne.
We’ll number from left to right to give the triple bond the number 1.
If we number from right to left, the triple bond would have the number 5.
So, we have 1-hexyne or hex-1-yne so far.
Now, we have to name and number the substituent.
The substituent is a methyl group at carbon 3 (carbon 2 isn’t easy to see but it’s at the end of the triple bond), so we would name it 3-methyl.
Putting it all together, we have 3-methyl-1-hexyne or 3-methyl-hex-1-yne.