Cycloalkene nomenclature?
Why is this 5-ethyl-3-methylcyclohexene and not 3-ethyl-5-methylcyclohexene when counting clockwise?
Why is this 5-ethyl-3-methylcyclohexene and not 3-ethyl-5-methylcyclohexene when counting clockwise?
How can I increase the concentration of sulfuric acid, for example?
Hi. I know this question has been asked here several times. However, I wanted to ask it in relation to my situation. Brief history: It's difficult for many people right now, since everything is so expensive. I (f, 18) have been freezing all afternoon and asked my mom if I could turn on the heating….
How can you tell that a chemical reaction has taken place?
I (f16) have been drinking now and again at parties or in the evenings for a long time. But lately the times when I drink have been increasing more and more. Maybe that's because it's summer. It's getting more and more out of control and I often do something embarrassing and extreme. Just last week…
Are there any drugs that have no health consequences or are harmless? I'm just curious; I don't want to consume anything.
How does trichloromethane react with chlorine? Is carbon tetrachloride formed? Would this be a method for producing CCl4?
Moin,
weil es gegen den Uhrzeigersinn
5-Ethyl-3-methylcyclohexen
ist, während es im Uhrzeigersinn gesehen
4-Ethyl-6-methylcyclohexen wäre.
Die Positionszahlen (3 / 5) sind kleiner als (4 / 6) und somit zu bevorzugen.
Das 5-Ethyl wird vor dem 3-Methyl genannt, weil E alphabetisch vor M kommt.
LG von der Waterkant
Die Doppelbindung muß die Atome 1 und 2 enthalten, also haben wir zwei Möglichkeiten, wie wir numerieren:
Wir nehmen die Version mit der kleinsten Lokante 3, also 5-Ethyl-3-methylcyclohexen.
Man gibt dabei den Kohlenstoffen der Doppelbindung die Lokanten 1 und 2. Wenn man das anwendet, dann hat man entweder 4-Ethyl-6-methyl… oder 5-Ethyl-3-methyl… Im zweiten Fall hat der Satz der Lokanten die kleinere Summe.