Bicyclic compounds | Alkanes, cycloalkanes, and functional groups | Organic chemistry | Khan Academy

[@Chrisreynolds0724199]

there is a special place in heaven for people like you.

[@We_Do_It_Liev]

Khan academy always coming in clutch yasssssssssssssssssssssssss ty!

[@Tiifa90]

hahah :D thank god I understand english pretty well.. I study Pharmazie in germany and there were no german videos about bicyclic compounds . You explained it so good thank you !

[@DAKSPALM]

Cool,I also study pharmacy in China

[@sheekastewart]

you're better than my teacher! thank you!

[@mannatthakur5541]

In the last example, the substituent can even get the lowest no. 2 if you simply start numbering from the lower bridgehead Carbon and move to its left.

[@mohamad-abdo]

thanx man i really appreciate this i have an exam 4 tomorrow

[@sriyarane8827]

very well and effectively explained

[@lmaoded9191]

Woww never seen this type of teaching before thanks

[@shambhaviroy1458]

Omg u r such a genius don't know where I wud be w/o Ur yt channel. Thanks a trillion

[@subhasischakraborty6663]

excellent understanding techniche , from India..

[@wenlihuang3846]

thanks a lot! finally understand how to name those polycyclos

[@jeremytuck9705]

It is norbornane, not norborane! Please Fix. Great videos, Khan Academy is the bomb.

[@shaikhhossain8773]

Excellent video to gain some basic idea regarding fundamental chemisry.thank u so muchh...

[@MadcapClover]

Fantastic !! Thanks from Canada !

[@englishpesunalumtamilandaa7774]

u re a king of teaching

[@gezas4134]

Dude you rock, can you make more of this or something with pyridine and pyrimidine naming?

[@jazminevaz-baker8647]

thank you so much, you really cleared this up for me!

[@meghparajaydeep3179]

I watch this video and I learing very much thank you sir.

[@AbhiShek-nv3vq]

Dude it was pretty helpful. Thanks 😉

[@miamiry8737]

Excellent explanation! Thank you so much!

[@NeekBlack]

life saver! thanks for the breakdown

[@defrenchie]

Good sir, I do believe that the common name for Bicyclo [2.2.1] heptane is Norbornane not Norborane.

[@Lilymar2011]

This was great. Thank you.

[@anurup502]

very nicelly xplained!!from india..dewas!;)

[@ace0931]

what if do you have functional group? And the functional group was on the Y path. Would you still count first in the X path?

[@bahatimusic2555]

that is what we appreciate

[@heba.mohammed]

thanks from egypt :))

[@huntersikari]

Sir Thank you very much for the video! can you please do more complex ones like tricycylo tetracyclo etcetera??

[@sumanprakashverma720]

U r damn good at this...

[@poowarasankurunathan6049]

Thank u so much. It helped me alot.

[@priyadharshini8259]

Thanks from india,,

[@elmanahmed6117]

It was really helpful

[@nguyenbichvan1532]

U r the best. THANK YOUUU

[@medoxhunter6699]

Good simple explanation thanks alot

[@vermoutha5200]

Thank you sir.! It was really helpful.! :)

[@LunaDanu1]

so helpful, thank you very much

[@Shubham_9898]

thank you so much💐

[@deva224]

Super boss!!!

[@chirayatabhattacharyya8140]

great man!

[@psingh4803]

Thanks alot 😊

[@crysis860]

this is beautiful

[@sauravpandey7459]

Thankue bhaiyaaaa 🙏🙏🙏😜😜😜😜 for your precious lecture

[@joseescobar3703]

Thank you! Los amo!

[@victorchimaobi7387]

Really helpful

[@v.k.sharma9240]

Wow thanks

[@ceasersilumbwe4358]

Thank you man

[@jainishtrivedi5189]

very nice explanation

[@luckotyga]

Thanks so much!!!!

[@husamidrees4609]

Thanks!

[@sineanhem]

Tks ^^ (greeting form Vietnam ^^)

[@usanayamkayan4258]

Thank you very much ^^

[@schleckr4782]

where are you getting the 2? count long path first

[@jerielgarcia5115]

My question is how do you draw such nice rings?

[@akarati72saxena98]

good video thnx a lot

[@hanigorgis8980]

you are verey smart

[@Laz321]

You have to number the longest chain first.

[@akarshanpatel7978]

very good

[@akshatawagh8711]

You are awesome

[@eyteen08]

thank you :)

[@jbouge86]

shoudln't you have a (-) between dimethyl and bicyclo? So 6,8-dimethyl-bicyclo[3.2.1]octane?

[@stargazer4023]

No there is usually no dash between the name of the last substituent and the parent alkane e.g. it's 3-ethyl-2-methyldecane never 3-ethyl-2-methyl-decane.

[@born2bee]

thank youuuuuuuuuu!!!

[@Georgiaboy_]

if the last carbon had substituents aren't those carbons as well?

[@eniolaabolade8638]

Why don't we count the substituents and add to the number of carbon atoms?

[@awesomechemistbyedward1506]

I LOVE YOU

[@thecolorofcolour]

You are an angel, man. Fucking love you.

[@edniagutierrez7171]

thaaaank you

[@ajithkumar4129]

Tq

[@thewwefan57]

Bicyclo *4.2.0*

[@chirayatabhattacharyya8140]

great job sir , you made my day ; what's your email id so that i can contact you? really liked your easier approach of teaching !

[@mohamad-abdo]

!!!!!

[@himanshushekhar899]

hindi nhi aata hai bancho

[@alaaallam9042]

very helpful, thank you

[@alaaallam9042]

very helpful, thank you