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Resonance structures for benzene and the phenoxide anion | Organic chemistry | Khan Academy 

Khan Academy Organic Chemistry
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Examples of how to draw resonance structures for molecules with aromatic rings. 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!
About Khan Academy: Khan Academy offers practice exercises, instructional videos, and a personalized learning dashboard that empower learners to study at their own pace in and outside of the classroom. We tackle math, science, computer programming, history, art history, economics, and more. Our math missions guide learners from kindergarten to calculus using state-of-the-art, adaptive technology that identifies strengths and learning gaps. We've also partnered with institutions like NASA, The Museum of Modern Art, The California Academy of Sciences, and MIT to offer specialized content.
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23 авг 2024

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Комментарии : 31   
@GigaChad_hmm
@GigaChad_hmm 6 месяцев назад
So far the best explanation I have ever seen , it's helping me out after 9 years .❤❤
@A1dakz
@A1dakz 6 лет назад
amazing how colour coding makes such big difference! Just had a confetti moment in my brain! Thanks :)))
@Youknowwho910
@Youknowwho910 Год назад
🎉🥳 i love this comment
@manjuprasannakumar2222
@manjuprasannakumar2222 6 лет назад
Thank you ...finally I understand the resonance structure of benzene..thank u once again
@ShowtimeHBOsports
@ShowtimeHBOsports 6 лет назад
This is extremely helpful! No one teaches better than this online. Keep up the GREAT WORK!
@RK-lo4qz
@RK-lo4qz 7 лет назад
no one can explain in this way
@mspinkflipflops5681
@mspinkflipflops5681 8 лет назад
this playlist is a life savior.. I can't be more thankful to the you for making that much effort!!! I completely neglected my complicated lecture notes to your very detailed and well-explained videos.
@user-gv1eo3oo8o
@user-gv1eo3oo8o 6 лет назад
MashAllah Thank u Hope Allah bless your work
@vid0302
@vid0302 6 лет назад
wowww, really simple and good instruction, Thank!
@zanyiakelly1982
@zanyiakelly1982 4 года назад
I love you Jay. Thank you so much, Khan Academy never fails!
@gamingwithmax402
@gamingwithmax402 5 лет назад
Thanks Khan Academy Finally Understood Resonance
@mushfiqborat113
@mushfiqborat113 6 лет назад
Benzene is a form of hydrocarbon of the arene group which consist of rings of Carbon atoms each with a single Hydrogen atom bonded to it. The atomic properties of carbon mean that each Carbon atom in these rings is missing one bond. This bond is exhibited in arene rings as a delocalised electron cloud around the whole ring, or as transient pi bonds which switch from atom to atom very quickly.
@dishanaaz5446
@dishanaaz5446 5 лет назад
It is toooooooooooooooo good.
@BOLYANA
@BOLYANA 5 месяцев назад
Manyyyyy thanks🙏🏻🙏🏻🙏🏻🙏🏻
@harisathiya3166
@harisathiya3166 2 года назад
Superb lecture..
@sauravkumar-ho4wv
@sauravkumar-ho4wv 5 лет назад
In benzene If I moved the electrons of pi bond on one of the carbon containing that pi bond as a lone pair electron creating formal negative charge and on other connecting carbon getting positive charge ? Is it a correct resonating structure of benzene ??
@samudrajs5409
@samudrajs5409 3 года назад
Really helpful
@sabrinruiya9764
@sabrinruiya9764 4 года назад
It's awesome 😍😍😍
@intertainerk.k
@intertainerk.k 2 года назад
Great
@AmanKumar-ny8hr
@AmanKumar-ny8hr 3 года назад
Thanks
@suhasmahamunkar6055
@suhasmahamunkar6055 5 лет назад
besttttt video loved it
@user-hq9oq5nl3w
@user-hq9oq5nl3w 3 года назад
great video
@aneleimmaculate412
@aneleimmaculate412 5 лет назад
thanks
@anshikachauhan3921
@anshikachauhan3921 5 лет назад
Bestt....
@1az2ww
@1az2ww 7 лет назад
the first arrow results in a violation of the octet, so how come it is acceptable? What are the exceptions
@1az2ww
@1az2ww 7 лет назад
at 2:52
@xLifeinmotionx
@xLifeinmotionx 6 лет назад
You say the first arrow and then you link to the second arrow. The reason the first arrow--where a lone pair coms off of Oxygen and forms the double/pi bond)--is allowed is BECAUSE the second arrow happens simultaneously. So, there's no violation of the octet rule.
@prasadkondedeshmukh4818
@prasadkondedeshmukh4818 8 лет назад
i did not get phenoxide anion reso sructures
@jamalkhan2305
@jamalkhan2305 5 лет назад
first it was a phenol ring, because phenol ring easily donate h ion thats why it become phenoxide ring,
@mostpopularvadios736
@mostpopularvadios736 4 года назад
Dr Ahmad Tutorials is much better vadio for resonance
@harshvardhanmankotia6492
@harshvardhanmankotia6492 3 года назад
I hate chemsitry
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