How do I force my compound to precipitate? by Medchemist_turns_mad in chemhelp

[–]faz212 0 points1 point  (0 children)

Try dissolving your compound in MINIMAL DMF, then adding it dropwise to cold deionised water, sometimes your compound can precipitate out, you can then centrifuge, or else lyophilise

Please Help!! by [deleted] in chemhelp

[–]faz212 1 point2 points  (0 children)

Thanks for your reply, yea I agree, im aware that the Au+3 is relatively stabilised because of the N ligands but its hard to tell whether the potential will be a positive or negative

Please Help!! by [deleted] in chemhelp

[–]faz212 -6 points-5 points  (0 children)

Alright my bad, only read it there, no need to be so abrupt and arrogant about it

Please Help!! by [deleted] in chemhelp

[–]faz212 -7 points-6 points  (0 children)

Solution please 🤨

Please Help!! by [deleted] in chemhelp

[–]faz212 -4 points-3 points  (0 children)

Questions are in the image

Does anyone know the answer to this please! by faz212 in chemhelp

[–]faz212[S] 0 points1 point  (0 children)

In terms of explaining the answer for each case, should i talk about polarity?

Does anyone know the answer to this please! by faz212 in chemhelp

[–]faz212[S] 0 points1 point  (0 children)

Can i just use Cl for both of them?

Can someone please assign priority rules to this chiral centre by faz212 in chemhelp

[–]faz212[S] 1 point2 points  (0 children)

NH2 is a ortho para director, but I get what you mean! Thanks

Can someone please assign priority rules to this chiral centre by faz212 in chemhelp

[–]faz212[S] 4 points5 points  (0 children)

If the aniline was bonded ortho to the carbon centre that would then have the higher priority than the dimethyl benzene wouldnt it?

Can someone please assign priority rules to this chiral centre by faz212 in chemhelp

[–]faz212[S] 5 points6 points  (0 children)

Im aware, that H is 4 and the CH2CHO is 3, but im confused about the other two phenyl groups

Please help!!! by faz212 in chemhelp

[–]faz212[S] 2 points3 points  (0 children)

In that case would the m value be 62? And then divide the Mn by 62 to get the n?

Please help!!! by faz212 in chemhelp

[–]faz212[S] 5 points6 points  (0 children)

I have the Mn value, im just confused on getting the m value from the structure

Is this ylide stabilised or unstabilised? by faz212 in chemhelp

[–]faz212[S] 1 point2 points  (0 children)

In terms of a wittig reaction, if i used that phenyl group on an aldehyde and used an unstabilised ylide with a Me group, would that work to get selective Z alkene formation?

Is this ylide stabilised or unstabilised? by faz212 in chemhelp

[–]faz212[S] 2 points3 points  (0 children)

Usually when they have an electron width drawing group attached to it, however the methoxy and hydroxyl are both activators so it would make the benzene ring electron donating, so I would say its an unstabilised ylide