Chemistry Connected was created by Laurie Starkey, Organic Chemistry Professor at Cal Poly Pomona.
For online organic chemistry lessons, visit Dr. Starkey's lectures at Educator.com
www.educator.com/chemistry/organic-chemistry/starkey
www.educator.com/chemistry/organic-chemistry-lab/starkey/
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what the fuck?
B will be syn or anti addition?
🙃I liked it
thanks
very informative! thanks!
Thank you so much omg
Roci or racimic i can't see d handwriting
amazing explanation!
Nice one
Thanks 😊
Enjoy Laurie
By chance it will have isolation of tannins
Sir my compounds are non polar compounds. so which solvent do I use for dissove the compound and what solvents do I use in the mobile phase? sir can you tell me a little bit? I am facing a lot of problems in tlc checking
Well summarized ❤
Djjdhdhfhv
This shows how short a conceptual video has to be ❤
Are the answers to the questions in the video somewhere ..?
Splendid!
Beautiful thanks!
Mucha Gracias
Thank you!
Thank you for this video.
i have a midterm next week; thank God i came across this!
What is the solvent used in addition funnel, is it water
@ChemistryConnected could you please provide me with the link for interactive TLC simulator
Thanks so much. I had trouble with these arrows even though my answers were right the whole time. You saved my grade!!
what a lovely video!!! I had so much fun watching😍😍
Wonderful....... God bless you.....
Ty❤
So polarity of Solvent + Component + Stationary Phase all impact Rf values?
for (I), wouldn't you have two compounds since both carbons are secondary carbons and so the bromine could either end up with carbon #3 or carbon #2 since they're equally stable?
ጥሩ ነበር ግን በደንብ አይታይም ጥራት የለውም ከኔ ከሆነ አላውቅም
This is a great resource. Thank for uploading it. Where do you get you handouts from?
This video is really underrated, the concepts were well explained, cleared .y confusion, thanks
Many of the neutral compounds could still be polar molecules, such as anything with a carbonyl. Even a carboxylic acid at acidic pH will still have a polar carbonyl group. So couldn't a significant amount of these still move to the water layer? I'm sure it depends on how hydrophobic the rest of the molecule is too, but acetone and ethanol are pretty water soluble, though I'm not sure what the equilibrium would be between water and say, hexane.
Thanks for the lecture...
Old video but very helpful with the explanations, I found it personally better than any Google page filled with info. Very much appreciated Ma’am.
Moles calculation were explained in simplest way..Thank you..
Your ENTIRE playlist on NMR spectroscopy is so amazing you've made learning the topic much simpler than my professor! Thank you so much!!!!!
Could you please guide me to synthesize methyl vinyl ketone, i mean with reaction conditions. Thank you
Is there another way to extract eugenol from clove oil? On an industrial scale. When you extract this way, do you lose the beta Caryophyllene that’s also in clove oil?
you can extract the cloves directly to make a tincture and distill it into its components, or you can extract the dried residue by using organic solvents. There are many phenolic acids in cloves, which you get from the aquous residue, perhaps following an acid hydrolysis of the residue... Just get going and you will see.
very good video
you didnt say which is which and didnt calc it -_-
「ビデオコンテンツはとても素晴らしいです、おめで
First year thank you
and if we have to calculate amount from equivalent?
Great explanation. Thank You !
Great explanation and information is systemized. Thank you.
Amazing. Thank you so musch it helpfull