Must Know Synthesis and Reactions of Acid Chlorides

Поделиться
HTML-код
  • Опубликовано: 12 янв 2025

Комментарии • 9

  • @VictortheOrganicChemistryTutor
    @VictortheOrganicChemistryTutor  8 месяцев назад +1

    Please, like, share, and comment to help promote this video!
    If you would like to support the channel, you can do so by either donating or becoming a member:
    Donate: www.organicchemistrytutor.com/donate/
    Membership www.organicchemistrytutor.com/membership/

  • @chemistryforsociety3448
    @chemistryforsociety3448 8 месяцев назад

    Excellent content.....

  • @NaveenRajendran-jb6ur
    @NaveenRajendran-jb6ur 8 месяцев назад

    Top notch

  • @NaveenRajendran-jb6ur
    @NaveenRajendran-jb6ur 8 месяцев назад

    Hey Victor Suggest some good channel for fundamental concepts of molecular spectroscopy

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  8 месяцев назад

      Lemme know if you find one 😆 I don’t know any, unfortunately. There’s a really good insta account called NMR Spectroscopy, he’s got some top notch stuff and posts a lot of really neat examples and challenges. Other than that, I don’t really know any social media or RUclips channels dedicated to spectroscopy. I am planning to significantly expand my spectroscopy section when I have time as making those videos takes entirely too long, so that’s in the back burner for the future for now.

  • @varunarora1256
    @varunarora1256 8 месяцев назад

    This was quite a good refresher.
    I remember a question I did which mentioned the use of one equivalent of grignard with an ester and acid chloride separately and made different products for both and I was dumbstruck 'cause I had always seen them as just electrophiles with leaving groups doing the same shit 😆
    BTW, doesn't potassium oxychloride and hcl eventually form phosphorous acid? Or is it got to do something with the reaction conditions?

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  8 месяцев назад

      You mean phosphorous oxychloride? Yes, it will upon treatment with water but you first need to get your acid chloride out (typically, by distilling it out). That’s the problem with those reactions as you have the “junk” stuck in your reaction mixture as opposed to thionyl chloride that makes gases and SOCl2 itself is easy to distill out if you have excess (it boils at 76°C while most chlorides have b.p. at 100°-200°C)

    • @varunarora1256
      @varunarora1256 8 месяцев назад

      @@VictortheOrganicChemistryTutor Yup I mean phosphorus. That was just dumb autocorrect
      I asked that 'cause I've seen just phosphorous acid as the side product without the mention of the predecessors you've shown

    • @VictortheOrganicChemistryTutor
      @VictortheOrganicChemistryTutor  8 месяцев назад

      A good exercise and a "sanity check" for a reaction is balancing it. If you have correct products, you'll always be able to balance it. Of course, you occasionally can balance nonsensical things too, but if your reaction is unbalanceable, it's a dead giveaway that it's wrong. For instance, I seriously doubt you'll be able to balance RCOOH + PCl3 or PCl5 ---> RCOCl + H3PO4 + HCl. Unless, of course, you conveniently "forget" about one or two co-products... then anything is possible.