Hemiacetals, Acetals, and Imines

[@carlasalas1932]

I learned more from this, than my lecture. Like Idk why there is such a lack of clarity in lecture, lol they go straight to explaining the mechanisms with examples without even stating what we're trying to make or what we're working with. You're videos are really saving my ass in Ochem, thank you.

[@j.dreessen8503]

My dude. 90 min lecture boiled down to a 7 minute video. You're the best!

[@monicachiodo3815]

i want to give you a hug

[@ProfessorDaveExplains]

hugs are much appreciated!

[@LexoG33]

Thank you, Dave! I have an exam on carbonyl chemistry coming up, and it should help to hear things explained in other words.

[@elifgoksualgn2744]

professor dave you are a life saver i love your videos so much and they help me understand everything perfectly. Youre amazing!!

[@clashpaper]

Professor Dave, this video is so concise and easy to follow I actually feel like I've misunderstood something.

[@Itz_ronny07]

Elegant explanation

[@abhiramagorti1803]

At 1:30 why does the OH group get protonated but not the OR group? Please answer me professor

[@hamedhosseini4938]

Thank you professor.

[@Vagdebrume]

Dude, I love your videos

[@monicachiodo3815]

i owe you my life

[@freeenergy7189]

could u pls make a video for(amines) reactions with sulfonyl chlorides to form sulfonamides and acylation with carboxylic acids and derivatives to form sulfonamides . THANK YOU

[@deekshajoshi8511]

Sir can you explain reactions of glucose with acetone

[@khidirmanwer2482]

thank you a lot prof.

[@DarlinaLiu]

During imine formation, can we represent the proton transfers by having the negatively charged oxygen pluck the hydrogen from the nitrogen... or that a bad idea?

[@ProfessorDaveExplains]

+Darlina Liu i wouldn't say it's specifically wrong, but it might be statistically unlikely.

[@mygsmolbean]

thank you so much professor! it helps me a lot. anyway i have a weird question.. whats gonna happen to imine if we give heat and KOH? will the oxygen's free electron attact the carbon in imine? thank you before

[@topgap49]

u really should make a video about dcc/dmap and mukaiyama

[@老铁哥]

Hi David, may you please do some video on Titration analysis(Multivariate acid-base titration) and Absorbance spectrophoto

[@annoyingwalker]

Could you explain how an imine is formed with an aldehyde instead?

[@ProfessorDaveExplains]

no difference!

[@Tamar839]

you are amazing

[@deekshajoshi8511]

Sir please tell how to deprotect these groups

[@ProfessorDaveExplains]

like the cyclic acetal that protects ketones/aldehydes? just a little acid

[@deekshajoshi8511]

Ok thanks

[@TheToxicMegacolon]

bless up bro

[@tariqfiqyat848]

i love u so much man

[@giseleho9730]

thank you o chem jesus, for your blessings

[@caitlinaschliman1849]

is it just me and my internet or is the audio and the video not in sync with each other?

[@ProfessorDaveExplains]

works fine for me! try refreshing.

[@jaykemm3472]

Sweet. But just here tryin to figure out how to turn water to wine.

[@johannagallistl2715]

i just fell in love with you

[@benjaminkoerper]

excess alcohol... I felt that

[@sumitsinghal6127]

Nalla

[@Risachanwww]

😭😭😭😭😭❤