Quick Revision - Esters

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  • Опубликовано: 2 дек 2024

Комментарии • 15

  • @aliananda6912
    @aliananda6912 2 года назад +4

    currently bingeing all your videos for my paper 2 mock on Monday !! :)

  • @thegreentoga1041
    @thegreentoga1041 6 лет назад +12

    life saver mate.

  • @noelle4145
    @noelle4145 2 года назад +2

    1:10 why was the third example named pentyl propanoate instead of propyl pentanoate ? Isn’t the part connected directly to the co double bond what comes from the original carboxylic acid? Meaning that this ester would have been made from propanoic acid ?

    • @MaChemGuy
      @MaChemGuy  2 года назад +1

      I drew that one the other way round to catch people out just like the exam boards do. Sorry

    • @noelle4145
      @noelle4145 2 года назад +1

      @@MaChemGuywait so how am I supposed to figure out what part of the chain tells me the first or second part of the name? 🥲

    • @MaChemGuy
      @MaChemGuy  2 года назад +3

      @@noelle4145 You called it in your first message. The part connected directly to the C=O is the oate part and the one connected to the C-O is the yl part

  • @ابوحمادة-ق8ن
    @ابوحمادة-ق8ن 7 месяцев назад

    Please, can I ask you about preparing ester oil?

  • @goodvoucerry
    @goodvoucerry 6 лет назад +1

    For esterification for carboxylic acid and alcohol do you just say heat or heat under reflux?

    • @jennyhart1918
      @jennyhart1918 6 лет назад +4

      Leveration Heat under reflux with a H2SO4 catalyst ♥️

  • @melleni
    @melleni 3 года назад +3

    Thank you very much

  • @rukayyasaifuddin6811
    @rukayyasaifuddin6811 6 лет назад +5

    love ya