Short question Does the product have an H instead of a CH3 group and are there charges in the second to last step on the C of R2C and on the Base in the third to last step of the general mechanism?
@Sally Sally his pronunciation is completely incorrect... as @Barbara O'Boyle mentioned, the K is silent. It's pronounced "No-ven-eygle," if that makes sense.
I had a very minor doubt that was causing a problem in further reactions. Thank you for explaining so clearly!
Short question
Does the product have an H instead of a CH3 group and are there charges in the second to last step on the C of R2C and on the Base in the third to last step of the general mechanism?
Excellent!
great gr8 gr8 gr8 thank you
Great!
nice lecture
Pay attention, why are you saying that the starting dicarbonyl is a lewis acid?
Bronsted
Is there a reason why you left the H off the final product?
Pay attention the starting dicarbonyl compound is not a lewis acid...
Mechanism of doebner modification ,please?
How do we pronounce Knoevenagel?!
Watch the video....but to make your life easier. 0:37 :-)
+AK LECTURES (Andrey K) plz can u plz help me by giving some synthetic apploications of knoevenagel rection urgently plz
Habiba Naeem the hantzch's dihydropyridines is an example.
The 'K' is silent.
@Sally Sally his pronunciation is completely incorrect... as @Barbara O'Boyle mentioned, the K is silent. It's pronounced "No-ven-eygle," if that makes sense.
Damn u sound angry on 1.5 Speed ahaha
please stop singing.