The mechanism was well explained, really loved that part. Organic chemistry is truly a beautiful part of chemistry as the experiments we can do with various reagents are truly limitless. A small request if possible to cover a lot of the reagents used in my ap class, at least the ones you feel important, as no matter how much I read extra some other reagents pop up in the exam which I'm unable to determine the mechanism of. Pls do help. Love the vids. Keep posting
Hey Dave, I reckon you should do a video with telltale about the psychological paranoia and the general mind on people obsessed with conspiracy theory’s. I reckon telltale would be a good person to collaborate with given his channel is about that sort of thing and I’m quite sure that he might have a psychology degree (although I faintly remember it being mentioned). Anyway, cheers! Don’t let the low (high for me) views stop you man, your a great inspiration to all for science.
Professor dave. i got a question about transition metal ions, do they retain their transition metal properties after they are in an ionization state where they no longer have a partially filled d-orbital (ie. Ti 4+, has no partially filled d orbital left, will it still produce a color when dissolved in water,etc.)
@@ProfessorDaveExplains Hmm, i see, in terms of different oxidation states it can create different colors, but how about the oxidation states that no longer contain any partially filled d-orbital like Ti 4+ or V 5+
@@justinjaya9268 It can often depend on what co-ion the metal is coordinated with. The d-orbitals are still available even if nominally empty and if the energy gap is right then the compound will absorb light at frequencies that give visible colours.
Dear Prof. Dave, I wonder what particular cells in the kidney produce HIF? Besides, what is the control center of red blood cell production? Many thanks! ( Or anyone who knows, could u plz kindly answer me? Quite confused...)
It’s Jesus here to save me from my failing class.
🤣🤣🤣🤣🤣
The mechanism was well explained, really loved that part. Organic chemistry is truly a beautiful part of chemistry as the experiments we can do with various reagents are truly limitless. A small request if possible to cover a lot of the reagents used in my ap class, at least the ones you feel important, as no matter how much I read extra some other reagents pop up in the exam which I'm unable to determine the mechanism of. Pls do help. Love the vids. Keep posting
life saver as always, thank you dave I owe you my first born
Informative and helpful, as always, Professor Dave. Thanks.
Nice , love from India.
Very nice, thank you for all series
very good information
thanks a lot professor , content is enough and excellent
Welp I’ve been pronouncing periodic acid wrong the whole time
Thank you sooo much sir !
Very helpful thank you
Thank you, that clarified a lot
Thank you
Hey Dave, I reckon you should do a video with telltale about the psychological paranoia and the general mind on people obsessed with conspiracy theory’s. I reckon telltale would be a good person to collaborate with given his channel is about that sort of thing and I’m quite sure that he might have a psychology degree (although I faintly remember it being mentioned). Anyway, cheers! Don’t let the low (high for me) views stop you man, your a great inspiration to all for science.
Thanks a lot professor wanted this video badly finally got it
I use this acid to cleave carbon-carbon bonds, periodically.
thank you 😊
How does formic acid form from the reaction of periodic acid and glycerol?
Hi Professor Dave!!
Professor Dave what is 2HIO4
two equivalents of periodic acid
3:50 How do Aldehydes get cleaved to become Formic Acid in this example? Does the Acylium ion HC(+)O steal (-)OH from the Periodate transition state?
Wow sir extremaly good ✌✌✌
It's not Periodic acid.
It's Per Iodic acid
It's one word. That's how prefixes work.
Please make a video about angle ,tortional and steric strain
and thank you
Professor dave. i got a question about transition metal ions, do they retain their transition metal properties after they are in an ionization state where they no longer have a partially filled d-orbital (ie. Ti 4+, has no partially filled d orbital left, will it still produce a color when dissolved in water,etc.)
the different ions produce different colors, even two different oxidation states for the same metal can produce different colors
@@ProfessorDaveExplains Hmm, i see, in terms of different oxidation states it can create different colors, but how about the oxidation states that no longer contain any partially filled d-orbital like Ti 4+ or V 5+
@@justinjaya9268 It can often depend on what co-ion the metal is coordinated with. The d-orbitals are still available even if nominally empty and if the energy gap is right then the compound will absorb light at frequencies that give visible colours.
Isn't that erythrose? Not Glyceraldehyde?
too good!
What is mechanism in case of other compounds where hydroxyl group is adjacent to carbonyl group i.e. glyceraldehyde & dihydroxy acetone ?
Damn, catfished by a science video... AGAIN.
Dear Prof. Dave, I wonder what particular cells in the kidney produce HIF? Besides, what is the control center of red blood cell production? Many thanks! ( Or anyone who knows, could u plz kindly answer me? Quite confused...)
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Thank you Jesus😊😊
wowwwww
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