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@joselyn.villelas: ✨🧡 - #hikes #fallvibes #henryhudson #fyp #asmr
Josiii🤍.
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Saturday 31 October 2026 18:50:45 GMT
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what does HBr do to the molecule that makes roses smell like roses? 🌹 search "inkling orgo" on the App Store or go to tryinkling.app the main smell of rose oil is phenethyl alcohol (2-phenylethanol), a benzene ring on a two-carbon chain that ends in an OH. this page is the exam problem: alcohol + HBr, parts a to d on slide 1, and today's in-app quiz is this exact problem, so the answers to a to d are not here. what is here is the full example on a different alcohol, tert-butanol + HBr, for orgo 1 midterm 2. an OH is a poor leaving group, so the HBr has to act first: the O's lone pair takes an H+, which makes OH2+, and water is a good leaving group. water then leaves on its own and leaves a 3° carbocation. that carbocation is stable because three alkyl groups share the + charge, so Br- bonds to it and you get tert-butyl bromide. a reaction that goes leaving group first, then nucleophile, is SN1. the rose is a 1° alcohol, and a 1° carbocation is too unstable to form, so the 3° story does not carry over. how 1° and 3° alcohols differ with HBr, and SN1 vs SN2 in general, is the heart of the midterm 2 question. part d is the one to commit to: SN1 or SN2 for the rose? 👇 #ochem #organicchemistry #sn2 #chemtok #studytok
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