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IiTeachChem

•Created by Nimboi on 3/18/2025 in #💭│doubts

Amines, organic conversion question

Hope this explains it

17 replies

IiTeachChem

•Created by Nimboi on 3/18/2025 in #💭│doubts

Amines, organic conversion question

Because when amine is treated with no2 it has a very low yield of nitroproduct

17 replies

IiTeachChem

•Created by Nimboi on 3/18/2025 in #💭│doubts

Amines, organic conversion question

Actually for the second one, treating the amide with so3h is commonly used when u want to substitute no2 at o and p, but it also can be used for bromine

17 replies

IiTeachChem

•Created by Nimboi on 3/18/2025 in #💭│doubts

Amines, organic conversion question

1) on heating so3h is attached at para 2) this is a common method to get bromine substituted at ortho/para the so3h dead teases the electron density in benzene which favours the substitution of bromine

17 replies

IiTeachChem

•Created by Say_miracle_shadow on 2/26/2025 in #💭│doubts

SN1 or SN2

KOH can be used for both SN1 and SN2, it depends on the substrate taken, here there is a possibility for a stable carbocation so I said SN1 Now if I were to take primary propanol or something, that time SN2 will take place Pls correct me if I am wrong

19 replies

IiTeachChem

•Created by Say_miracle_shadow on 2/26/2025 in #💭│doubts

SN1 or SN2

SN1

19 replies

IiTeachChem

•Created by hardcoreisdead on 2/15/2025 in #💭│doubts

ortho para directing

Nvm didn’t read the Q fully

65 replies

IiTeachChem