Interpretation:The major product of addition of bromine to
Concept introduction:Alkenes are considered electron-rich and undergo bromination addition reaction with
The mechanism of
In the second step, the strained bromonium ion intermediate opens while
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- You are planning to carry out a reaction between propyne, CH3C≡CH and sodium amide, NaNH2. You also need to choose an appropriate solvent for carrying out the reaction. Would ethanol be suitable for this purpose? Explain your rationale clearly.arrow_forwardDraw and name the thee steps of the mechanism of the bromination reaction of 1,2-diphenylethane.arrow_forwardOutline the possible reaction pathways with proper mechanism for the formation ofNylon 6 from Benzene molecule.Q2.arrow_forward
- p-Fluoronitrobenzene is more reactive toward hydroxide ion than is p-chloronitrobenzene. What does this tell you about the rate-determining step for nucleophilic aromatic substitution?arrow_forwardOutline the step-by-step method (initiation, propagation(s), and one termination step) for bromination of 2-bromopropane to produce its major product.arrow_forwardWrite the reaction mechanism E2 between 2-bromopropane with sodium hydroxide, NaOH.arrow_forward
- Provide a synthetic strategy for the construction of molecule Q from molecule R. You may use any reactants/reagents/conditions that are necessary for your synthesis to be successful. متجر онс CHO CN CH, R Provide conditions and a viable mechanism that would explain how molecule D can be converted into molecule C. -os CH,arrow_forwardFollowing compounds are given to you:2-Bromopentane, 2-Bromo-2-methylbutane, 1-Bromopentane(i) Write the compound which is most reactive towards SN2 reaction.(ii) Write the compound which is optically active.(iii) Write the compound which is most reactive towards β – elimination reactionarrow_forwardDescribe the mechanism by which benzene is converted to bromobenzene (C6H5Br) on treatment with a mixture of bromine and iron (III) bromide (Br2/FeBr3). Your answer should illustrate how the electrophile (Br*) is formed from the Br₂/FeBr3 and how it is involved in the electrophilic substitution of the aromatic ring.arrow_forward
- Like other hydroborations, the reaction of alkynes with catecholborane is a syn addition and its regioselectivity is opposite to Markovnikov’s rule.Use this fact to outline a synthesis of the compound shown from 1-hexyne and (Z)-C6H5CH=CHBr.arrow_forward(c) Outline the mechanism for the bromination of 3-methylcyclobutene.arrow_forwardThe following compounds are given to you:2-Bromopentane, 2-Bromo-2-methylbutane, 1-Bromopentane(i) Write the compound which is most reactive towards SN2 reaction.(ii) Write the compound which is optically active.(iii) Write the compound which is most reactive towards P-elimination reaction.arrow_forward
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