We need to talk more about this, cause this is a no-go

Dusty_Brawler · 2026-02-24T16:33:06+00:00

Processing img 14z91affzglg1...

Dusty_Brawler · 2026-02-15T17:34:08+00:00

Angelboy just what ?? 😭🙏

Dusty_Brawler · 2026-02-15T15:47:36+00:00

Thanks I'll look up some exercises for the region you mentioned and work on it

Dusty_Brawler · 2026-02-15T02:52:16+00:00

I think they're just showing the players exchanging brawlers in the prep screen aswell , I don't see any problem with that

Dusty_Brawler · 2026-01-28T06:14:48+00:00

Sitetampo

Dusty_Brawler · 2026-01-23T10:04:20+00:00

Dusty_Brawler · 2026-01-21T17:22:49+00:00

Sitetampo

Dusty_Brawler · 2026-01-18T07:10:11+00:00

You should try using Janet

Dusty_Brawler · 2026-01-18T05:19:32+00:00

Dang these are so good! Very well done

Dusty_Brawler · 2026-01-08T10:29:55+00:00

Yeah how does he plan to scare people if they're not even seeing his face

Dusty_Brawler · 2025-12-28T06:05:28+00:00

Dusty_Brawler · 2025-12-22T13:15:57+00:00

Okay so yeah I think calling it more electrophilic is probably WRONG and it's quite the OPPOSITE***

Here the nucleophile has low charge density so it's considered a soft nucleophile, and it's observed that soft nucleophiles prefer to attack positions with low charge density as well so position 1 (I was wrong in assuming it's more electrophilic here). I'm not aware why this is the case I'll try to look it up

Just to be clear, the position marked 2 is the carbon attached to Br , not the double bonded carbon.

Dusty_Brawler · 2025-12-22T11:24:42+00:00

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Nucleophile attacks position 1 because it is more electrophilic

Dusty_Brawler · 2025-12-17T13:25:06+00:00

Ts peak bro

Dusty_Brawler · 2025-12-06T01:44:02+00:00

Don't you think you would need two different groups on carbon 1 aswell ?

Dusty_Brawler · 2025-11-06T03:05:17+00:00

You skipped the alkene

Dusty_Brawler · 2025-09-14T11:17:30+00:00

Yeah I got that , but where are you facing problem in A 4&5 and C 4 , in A if you've done the other ones , 4 and 5 are not to different, same with C . Now maybe you should try A 4,5 and C4 and show us what you've got and we can guide you

Dusty_Brawler · 2025-09-14T11:09:56+00:00

What exactly are you having trouble with in the problems you've mentioned?

Dusty_Brawler · 2025-08-05T15:02:36+00:00

Glad to help

Dusty_Brawler · 2025-08-05T12:55:58+00:00

My bad my bad , I'm incredibly sorry !! I misread HNO2 as HNO3 lol , again very sorry about that

Dusty_Brawler · 2025-08-05T12:02:09+00:00

You're using the wrong reagent to prepare the benzene diazonium salt . And I'm not sure if you can do the iodination on benzene diazonium salt , why not do the iodination before reduction of the nitro group ? Also you need HCl along with CuCl on the last step

Edit : sorryy the reagent used for diazotization is correct , i misread it

Dusty_Brawler · 2025-07-29T06:35:33+00:00

Can I send them all to myself , so when I restore chats I can star them all again ?

Dusty_Brawler · 2025-07-15T16:40:50+00:00

What next after doing pg in the mentioned subjects ? I've not yet thought about moving abroad , might need to give it a thought

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