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Chemistry
bromination of propylbenzene gives 1-bromopropylbenzene instead of 2-bromopropylbenzene or 3-bromopropylbenzene upon reaction with N-bromosuccinimide in precence of benzoyl peroxide as a radical initiator
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Are you asking why? If you are the benzyl radical (Ph-CH.CH2CH3)is the more stable of the three possible.
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Suggest a solvent pair for N-Bromosuccinimide using the following solubility data.
Solubility of N-Bromosuccinimide (g/100g of
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Ah, finding the perfect solvent pair for N-Bromosuccinimide, huh? Well, let me put on my chemistry
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I was wonder what bromine/glacial acetic acid solution is used for during the bromination of acetanilide reaction
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http://www.reference.com/motif/science/mechanism-of-bromination-of-acetanilide
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To calculate the theoretical and percent yield for the bromination of E-stilbene, you need to know
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Please write the chemical equation and calculate the reaction enthalpy (or energy) for the total bromination (addition of
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To determine the chemical equation and calculate the reaction enthalpy for the total bromination of
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what is the lewis structure for N-bromosuccinimide?
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We can't draw structure on this forum but here is a site that give the structural formula. You can
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Show all steps with reagents how you would synthesize propylbenzene from benzene.
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We would use a Friedel-Crafts alkylation of benzene: Benzene + 1-chloropropane ---> Propylbenzene +
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Hi guys,
I thought it would be due to aromaticity breaking difficulty? In the bromination reaction, why are the double bonds
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I think you are right. The aromatic ring has extra stability due to resonance.
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What is the effect of using cyclohexane as the solvent in the bromination of acetanilide?
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Go to the library! :))
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Explain why bromination of cyclohexene produces trans 1,2-dibromocyclohexane.
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The bromination of cyclohexene produces trans 1,2-dibromocyclohexane because of the concerted
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