Very nice video! Maybe you could also make a separate video testing out its energetic properties when dry. be careful if you do though, we wouldn't want to lose our beloved Vibz! ;D
I plan on making some benzyl chloride soon (need to make the anhydrous zinc chloride catalyst first). Then I may be able to try this :-) great video!! P.S. the quality of your videos is really improving.
I think you got me correcting my own pronunciation, when you said ethyl alcohol, as in ethanol, I heard the hard y like as if you said alkyne so my head went right away to an alcohol with a triple bond that can't exist (I even had to check). Then I realized, *that's* how *I'm* *supposed* *to* *pronounce* *it* isn't it😉
is the Dinitration due to temperature in this procedure or the amount of nitric acid. how would one preform mononitration of already formed p-nitrochlorobenzene?
Characterisation of aldehydes and ketones, due to their insoluble addition compounds with 2,4-DNPH, that usually have a sharp melting point. This, alongside other typical derivatives like oximes and semicarbazones, is how chemists characterised aldehydes and ketones in the old days before modern advanced chromatography techniques and NMR n shiet.
Very nice video! Maybe you could also make a separate video testing out its energetic properties when dry. be careful if you do though, we wouldn't want to lose our beloved Vibz! ;D
I plan on making some benzyl chloride soon (need to make the anhydrous zinc chloride catalyst first). Then I may be able to try this :-) great video!!
P.S. the quality of your videos is really improving.
? you need chlorobenzene, not benzyl chloride
I think you got me correcting my own pronunciation, when you said ethyl alcohol, as in ethanol, I heard the hard y like as if you said alkyne so my head went right away to an alcohol with a triple bond that can't exist (I even had to check).
Then I realized, *that's* how *I'm* *supposed* *to* *pronounce* *it* isn't it😉
Very nice synthesis. Btw, was that water washing of the 2,4-dinitrochlorobenzene enough to separate out any side products from the reaction, if any?
I love this color😍
I never stored it wet lol
is the Dinitration due to temperature in this procedure or the amount of nitric acid. how would one preform mononitration of already formed p-nitrochlorobenzene?
Could we prepare it from direct nitration of phenyl hydrazine?
What it's use in making other compounds ?👍
Characterisation of aldehydes and ketones, due to their insoluble addition compounds with 2,4-DNPH, that usually have a sharp melting point. This, alongside other typical derivatives like oximes and semicarbazones, is how chemists characterised aldehydes and ketones in the old days before modern advanced chromatography techniques and NMR n shiet.
Holy crap... you got this up fast! Lol
@@vibzzlab no, thank _you_ for the awesome content. I definitely want to try this synth out.
Sir auramine o making procees
Wasn't it hydrochloride salt that formed?
Dinitrobenzene reduction video
@@vibzzlab can you give the link sir thank you very much
@@vibzzlab thank you sır 😊😊😊😊
yaw dayı oğlu o profil ne ak padişah resmi aha türk dedim ayak mayak asjdkjaskdasd
Notes send me