"What Is the Iupac Name of the Following Compound?"

"What Is the Iupac Name of the Following Compound?"

"What Is the Iupac Name of the Following Compound?"とは一体何なのか? 主要なファクトを丁寧に紐解いて紹介します。

Side groups are like molecule accessories. You’ll see things like “methyl” (one carbon stuck to the chain), “ethyl” (two carbons), or “chloro” (a chlorine atom). These get added as prefixes, and you list them in alphabetical order. Yes, alphabetical—even if it means “ethyl” comes before “methyl” because ‘e’ is before ‘m’. English class meets chemistry lab!

And if there are two of the same side group, you use di-, tri-, tetra- (like “dimethyl” meaning two methyl groups). But here’s the funny part: those counting words don’t count for alphabetizing. So “dimethyl” still goes under ‘m’ for methyl. Don’t ask why—it’s just the rule, like how pineapple on pizza is still pizza.

Step 4: Put It All Together

Okay, time for the big finale. You write: number for the side group location, prefix for the side group name, then the parent chain name. Example: 3-methylhexane. That means a methyl group is attached to carbon number 3 of a six-carbon chain. Say it out loud: Three-methyl-hex-ane. It’s like a chemical chant.

If there are multiple groups, separate numbers with commas and groups with dashes. Like 2,3-dimethylpentane. That’s two methyl groups on carbons 2 and 3 of a five-carbon chain. Rolling off the tongue, isn’t it? You could even rap it—though I don’t recommend that at parties.

前田 葵
Author

前田 葵

マーケティングと消費者心理のトレンドを分析し、現代のヒット商品の背景を読み解きます。