more ape 3 | iTeachChem | Page 1

tepid oxide Jul 3, 2025, 3:53 PM

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WhatsApp_Image_2025-07-03_at_20.51.04_1.jpeg

verbal mulchBOT Jul 3, 2025, 3:53 PM

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<@&1227988359910260737>

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Note for OP

+solved @user1 @user2... to close the thread when your doubt is solved. Mention the users who helped you solve the doubt. This will be added to their stats.

neon patio Jul 4, 2025, 4:14 AM

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tepid oxide

A->S, B->PRS, C->P,S ?

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d ka nahi aa rha hai

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D ka im getting R as one of the options

blazing python Jul 4, 2025, 5:28 AM

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D ka shayd P,R hoga

shut skiff Jul 4, 2025, 5:56 PM

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A) me ek acid banega and ek methyl carbinol

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Basically CH3 uske agle carbon pe OH

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So it can give haloform

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Ester hydrolysis hai to acyl cleavage

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Also chiral centre hai us alcohol me so racemic mixture

shut skiff Jul 4, 2025, 5:59 PM

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shut skiff Ester hydrolysis hai to acyl cleavage

(Mechanism me it would occur)

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B) option…..

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B me bhi same as A)

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C) me carbocation formation hoga ‘cause first protonation of that ether vala oxygen

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Followed by bond breaking towards oxygen

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Then tert butyl cation formation

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Racemic mixture nahi banega C me

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Acyl cleavage nahi

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But haloform de dega

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Isme D option will generate a chiral centre
Vo D vaale carbon pe
So racemic mixture

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D option me 2 cleavage hain
Extreme left side vala would be SN2 (‘cause primary carbocation banega if SN1)

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Middle vala is SN1 (‘cause benzylic carbocation)

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So carbocation formation is there

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No acyl cleavage in D
Product doesn’t give haloform

blazing python Jul 4, 2025, 6:27 PM

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concise ans ..

shut skiff Jul 4, 2025, 6:51 PM

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blazing python concise ans ..

I’ve explained everything 😭

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I hope it’s easy enough to decode what options match and what don’t as I’ve discussed each one separately

tepid oxide Jul 17, 2025, 1:16 AM

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+solved @shut skiff

#more ape 3