When drawing the structural formula for compounds like 2-methylbutane or 2,3-dichloro-2-methylbutane, it is essential to start counting from the end of the chain that gives the lowest number to the prioritized functional group. This is a standard convention in organic chemistry. For alkenes and alkynes, the double or triple bond should also receive the lowest possible number in the chain. For example, a chain can be counted in two directions, resulting in different names like pent-1-ene or pent-4-ene, with pent-1-ene being the correct designation due to the lower number assigned to the double bond. Additionally, when naming substituents off the parent chain, they should be assigned the lowest numbers possible and listed in alphabetical order. If a benzene is present, it should also be given the lowest number. Understanding these naming conventions is crucial for accurate chemical nomenclature.