Alkane and cycloalkane nomenclature III | Organic chemistry | Khan Academy

Practice naming hydrocarbons with branches and rings. Also discusses classification of carbons: primary, secondary, tertiary, and quaternary carbons. Created by Jay.
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Organic Chemistry on Khan Academy: Carbon can form covalent bonds with itself and other elements to create a mind-boggling array of structures. In organic chemistry, we will learn about the reactions chemists use to synthesize crazy carbon based structures, as well as the analytical methods to characterize them. We will also think about how those reactions are occurring on a molecular level with reaction mechanisms. Simply put, organic chemistry is like building with molecular Legos. Let's make some beautiful organic molecules!
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Пікірлер: 19

  • @MotumaKaba
    @MotumaKaba11 жыл бұрын

    easy and clear way of lecture, thank you

  • @MuhammadAminNasir-SecurityERYK
    @MuhammadAminNasir-SecurityERYK4 жыл бұрын

    Wonder ful..made it easy

  • @user-be4yc2vr5c
    @user-be4yc2vr5c4 жыл бұрын

    I finally understand this now. Thank you! =p

  • @goobtron
    @goobtron11 жыл бұрын

    At 11:20 you explain how the sec-butyl comes from the secondary carbon and ignore the third on the alkane, but at the end of the video on the cycloalkane molecule you call the same sec-butyl carbon tertiary. Which is it?

  • @freezytestudo
    @freezytestudo2 жыл бұрын

    thank you so muchhh

  • @pacifiqueemmanuel1667
    @pacifiqueemmanuel16672 жыл бұрын

    Very interesting 👌

  • @Letmewatchsomevideos
    @Letmewatchsomevideos9 жыл бұрын

    why is the molecule to the left @ the 3:47 considered 1-methylpropyl? shouldn't it be considered butane?

  • @hsayrey

    @hsayrey

    8 жыл бұрын

    +Adam Thedon When you start numbering the carbons you have to start from the carbon attached to the original chain. From there he went to the side with the longest chain which was a total of 3 carbons(propyl) with one substituent which was the methyl on carbon 1.

  • @carlyallen768
    @carlyallen7687 жыл бұрын

    at 6:16 why isn't it 2 methylbutyl? That's the lowest number for the substituent ? You did that for the explain before why didn't you do it for that one?

  • @rwayle

    @rwayle

    7 жыл бұрын

    With side chains such as these, the #1 carbon is the one that connects to the parent chain, which is what the zigzagged line is.

  • @consolle2846

    @consolle2846

    4 жыл бұрын

    yea cought it too... and happy that encountered with ryan answer!

  • @apokange
    @apokange11 ай бұрын

    🙏🤝

  • @hardeeshah2858
    @hardeeshah28588 жыл бұрын

    why is it 1-methyl ethyl ? according to the rule, we need to go with ethyl first ?

  • @johnreed5225

    @johnreed5225

    7 жыл бұрын

    The methyl is the branch of the ethyl branch. Think of the ethyl branch acting similar to the main branch with the methyl group sticking out. If you had hexyl branch which also had a methyl branch and an ethyl branch then I think the rule applies. Correct if Im wrong

  • @abigailaddah1043
    @abigailaddah1043 Жыл бұрын

    Y 1 methyl ethyl

  • @ursulasolorzano
    @ursulasolorzano11 жыл бұрын

    i thought iso meant different

  • @nethajid9104
    @nethajid91044 жыл бұрын

    😑

  • @anamikasharma3607
    @anamikasharma36076 жыл бұрын

    2:05 can't we name it 4proply haptane?

  • @Sind.13
    @Sind.1311 ай бұрын

    Who's here??? 2023