Aromatic, Antiaromatic, or Nonaromatic - Huckel's Rule - 4n+2 - Heterocycles

[@TheOrganicChemistryTutor]

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[@kritika7386]

Can someone please explain how naphthalene is conjugated? I didn't get it For reference go to 6:51

[@henriqueserra3233]

same, it has 2 single bonds together right?

[@henriqueserra3233]

Just saw it better, it is conjugated, the upper double bound conjugates with the other 2 single bonds at its right

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Why is the molecule at 5:40 cyclic? I thought cyclic meant it had to be in a six membered ring form.

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Cyclic just means a ring not inherently 6 membered ring

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[@TheYoungFactor]

@8:17 how can you say it's conjugated when there is no pi bond below 4?

[@kaeya839]

It is completely conjugated because each carbon is sp^2 hybridized --> draw the resonance structure for the compound you will realize that the carbon below 4 will obtain the pi bond until and you keep getting equivalent resonance structures that you will end up drawing a circle eventually.

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[@dianamorad6334]

what does it mean that a pi-electron is 'free'? (0:43)

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It is delocalised

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They move throughout the benzene ring easily

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How can you tell if the carbon is sp2?

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When it makes double bond .

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Life saver

[@alostcat247]

thank you for the video! but i have a question if anyone can answer, i see an sp3 hybridization next to 4 in naphthalene and doesn't it mean it's nonaromatic? (pls answer respectfully🤍)

[@paysonkeown2960]

Every carbon in naphthalene has 3 groups attached to it so every carbon is sp2 hybridized.

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[@isaaya5631]

Is the last one nonaromatic or antiaromatic? Since, he said it was cyclic it should have been antiaromatic. can someone explain?

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THANKS :D