Could you explain why the last question for the aromaticity part is considered anti? I thought it would be non-aromatic because the N is sp3 and this wouldn't change with resonance.
I meant non-Aromatic because nitrogen is sp3 and there is no p orbital on nitrogen to make resonance with pi electrons so this ring is not fully conjugated.
Dr. G don't make the test to hard please i need at least a 62 to end with an A in ochem
anyone else studying at 3am hahahaha im having so fun !! 😹😹😹😹😹😹😹😹😹
so much studying i think i will take a quick 20 minute nap 😇😇
hello vro
@@danylagunes5307
Could you explain why the last question for the aromaticity part is considered anti? I thought it would be non-aromatic because the N is sp3 and this wouldn't change with resonance.
I meant non-Aromatic because nitrogen is sp3 and there is no p orbital on nitrogen to make resonance with pi electrons so this ring is not fully conjugated.
I have a question regarding problem 1. We do not have a Chlorine halogen in the compound since the isotope peak is not a 3:1 ratio, correct?
That is correct but the question already mentioned that the compound X is a hydrocarbon and only contains carbon and hydrogen atoms.
@@orgtubeR Alright, thank you👍👍