a = Proton transfer d = SN2 Nucleophilic substitution g = Nucleophilic subs at carbonyl(acyl Xfer) b = Lewis acid/base e= Electr
ophilic aromatic substitution h = Conjugate (nucleophilic) addn c = E2 elimination f = Carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. n(nh3)3
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- Due to the inability of the reaction to take place, the yield of 1-Bromobutane would drop.
- Since 1-Butanol won't react with the additional sodium bromide, bromination won't happen.
- If water had been supplied, the equilibrium would have shifted extremely far to the left, preventing the reactants from interacting with the acid and favoring the yield of 1-bromobutane instead.
- When a substance undergoes bromination, bromine is added to the compound as a result of the chemical reaction.
- After bromination, the result will have different properties from the initial reactant.
- For example, an alkene is brominated by electrophilic addition of
.
- Benzene ring bromination by electrophilic aromatic substitution.
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