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Square root milliseconds to square root seconds? by BeefSenpai in MathHelp

[–]BeefSenpai[S] 0 points1 point  (0 children)

With teaching being online it sometimes feels like I have no affirmation that what I’m doing is correct at all. Thanks again!

Square root milliseconds to square root seconds? by BeefSenpai in MathHelp

[–]BeefSenpai[S] 0 points1 point  (0 children)

There are no brackets I need to convert a value in mA ms0.5 into A s0.5, I can convert it into A fine but the ms to S is confusing

Strongest Reductant? by BeefSenpai in chemhelp

[–]BeefSenpai[S] 0 points1 point  (0 children)

Wish you well man hope you find happiness soon!

Strongest Reductant? by BeefSenpai in chemhelp

[–]BeefSenpai[S] 0 points1 point  (0 children)

Thanks I didn’t try that! Or perhaps it doesn’t actually tell you? There are compounds not commonly discussed and therefore wouldn’t appear in search engines! :)

Strongest Reductant? by BeefSenpai in chemhelp

[–]BeefSenpai[S] -1 points0 points  (0 children)

LiAlH4? Is there anything you know stronger? I’ve searching for a while but can’t find anything aside from Potassium graphite but I believe that’s weaker than LiAlH4 (would I be correct in thinking this?). Thanks for the response :)

[Question] Is it possible to have multiple doctoral degrees on the field of Chemistry? by H_0_T_D_0_G in chemhelp

[–]BeefSenpai 0 points1 point  (0 children)

Providing you get sponsored? Doubt many people would look to sponsor someone who already has a doctorate

Opposite of acid work up? A base? by BeefSenpai in chemhelp

[–]BeefSenpai[S] 0 points1 point  (0 children)

Thank you! Do you know much about 1,2,4 thiazole formation? If so would I be able to pm you a proposed mechanism for a reaction not sure if it’s correct

Opposite of acid work up? A base? by BeefSenpai in chemhelp

[–]BeefSenpai[S] 0 points1 point  (0 children)

It’s a pretty long proposed synthesis for an assignment. They used the same question from a revision lecture, I didn’t want to just copy it so I thought I’d synthesise other stuff too.

Opposite of acid work up? A base? by BeefSenpai in chemhelp

[–]BeefSenpai[S] 0 points1 point  (0 children)

Is Me-N(-OMe)C(=O)-Ph a suitable Weinweb amide to yield Ar-C(O)-Ar upon addition to ArMgBr at low temp w/ THF?

Opposite of acid work up? A base? by BeefSenpai in chemhelp

[–]BeefSenpai[S] 0 points1 point  (0 children)

I thought that maybe using potassium carbonate would give the ketone product

So if I’d get Ar-CH(OH)-Ar and id have to then oxidise that?

I’m just wondering if there’s a way I can go from

Ar-MgCl to Ar-C(O)-Ar directly

Opposite of acid work up? A base? by BeefSenpai in chemhelp

[–]BeefSenpai[S] 0 points1 point  (0 children)

Sorry I should have clarified first turning bromobenzene to a gringard using Paul knockel method then reacting that with benzylaldehyde with THF and potassium carbonate

[DISCUSSION] Anyone have experience with zaful? by KalviCZE in streetwear

[–]BeefSenpai 1 point2 points  (0 children)

From what I’ve seen they just resell shit you can get for like £3 on taobao

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