Orgo 2 Practice Exam Q5 Benzene Multi Step Synthesis EAS and more

Orgo2Q5: Multi-Step Synthesis creating a disubstituted benzene product followed by additional reaction steps.
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Пікірлер: 9

  • @mekdesbelete8766
    @mekdesbelete87663 жыл бұрын

    you are the most brilliant teacher

  • @Leah4sci

    @Leah4sci

    3 жыл бұрын

    Thanks!

  • @deepyaa3392
    @deepyaa33922 жыл бұрын

    Can we say that the para is major in the nitration as there might be steric hinderance in ortho position?

  • @Leah4sci

    @Leah4sci

    2 жыл бұрын

    Yes, I can agree with that. Sterics will play a small role in the balance of the two products.

  • @gabriellaspirelli6954
    @gabriellaspirelli69544 жыл бұрын

    i thought NaNO2 would give us azide N2+

  • @brianng4933

    @brianng4933

    2 жыл бұрын

    It creates a species called a diazonium salt, and as she said in the video, it spontaneously breaks from the ring because N2 is a very entropically-favored gas, and then creates the vinylic carbocation.

  • @Leah4sci

    @Leah4sci

    8 ай бұрын

    👍

  • @demetrioshill8484
    @demetrioshill8484Ай бұрын

    Why does H30+ donate an OH group and not just an H?

  • @Leah4sci

    @Leah4sci

    29 күн бұрын

    That's a great question! If we think about it mechanistically, the positive carbocation on the benzene ring would be attracted to the partially negative oxygen over a positive hydrogen. It's the oxygen (and not the hydrogen) of H3O+ that should attack. Your professor will probably not require you to know the full mechanism for something like this, but you can at least think about how the opposite charges will attract.