UltimaOnline SG https://www.dropbox.com/s/nbb33pfyobl68uj/20161005_233018.jpg?dl=01. LiAlH4 in dry ether2. followed by H2O/ heat? no need heat right? Optional.
Flying grenade SG https://en.m.wikipedia.org/wiki/Cyclobutadieneis cyclobuta-1,3-diene aromatic? why not? all C atoms in cyclobuta-1,3-diene are sp2 hybridised right?
Flying grenade SG The pi electron energy of cyclobutadiene is higher than that of its open-chain counterpart, 1,3-butadiene, and it is therefore said to be anti-aromatic rather than aromatic. The rectangular structure is consistent with the existence of two different 1,2-dideutero-1,3-cyclobutadiene stereoisomers. This indicates that the pi electrons are localized and therefore not considered to be aromatic.
Flying grenade SG Polyenes are poly-unsaturated organic compounds that contain at least three alternating double and single carbon–carbon bonds. These carbon–carbon double bonds interact in a process known as conjugation.
Flying grenade SG 2 methyl groups joined to one carbon or 1 ethyl group is more electron donating by induction?
Flying grenade SG https://en.m.wikipedia.org/wiki/1,4-Benzoquinonebenzoquinone can have resonance?cks say so
UltimaOnline SG 2 methyl groups joined to one carbon or 1 ethyl group is more electron donating by induction?
UltimaOnline SG https://en.m.wikipedia.org/wiki/1,4-Benzoquinonebenzoquinone can have resonance?cks say so Have resonance, but no aromaticity.
Flying grenade SG cks say trans form more than cis https://www.dropbox.com/s/ij42vz0qidnr17e/20161006_122453.jpg?dl=0i still love ur previous post
Flying grenade SG https://www.dropbox.com/s/fspcryinswek27q/20161006_122808.jpg?dl=0 https://www.dropbox.com/s/mcg0k777iuz11rf/20161006_122757.jpg?dl=0
Flying grenade SG cks wrote slow in All his sn2 mechanism https://www.dropbox.com/s/chan9dxxawjj1cu/20161006_123319-1.jpg?dl=0
Flying grenade SG https://www.dropbox.com/s/nu04p9d3tkvhbox/20161006_125259.jpg?dl=0 pg 194what product will form when ester, amides, acyl halides react with 24dnph, Nu Sub to give what?
Flying grenade SG why is OH- hydroxyl group a better leaving group than carbanion R- or hydride H- ? OH- is also a strong nucleophile like R- and H- right ? cks say due to the above reason, aldehydes and ketone undergoes nu add, carboxylic acid undergo nu sub
Flying grenade SG https://www.dropbox.com/s/hld2siryk5xcyxt/20161006_135648.jpg?dl=0how do we know which substituent group is dominant?and in this case cks writes weakly activating CH3 groups dominate the strongly deactivating NO2 group ?
Flying grenade SG e- from NO2 group can delocalise into b.ring of nitrobenzene too right? https://www.dropbox.com/s/akatwjm0cr5ytdx/20161006_144236.jpg?dl=0
Flying grenade SG he writes NaBH4 can be put in aqueous soln https://www.dropbox.com/s/oogvzztova57mf1/20161006_152832.jpg?dl=0
