In radical reactions, there are sometimes non-halogenated side products formed from other termination steps. Choose the possible side product of the reaction shown below? Br2 hv A B 11 C III III IV IV D
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- What is the mechanism to get from the reactant to the productsThere is great excess of H2O in this reaction.methanol + CH3OH Suppose you were told that the above reaction was a substitution reaction but you were not told the mechanism. Evaluate the following categories to determine the reaction mechanism and then draw the structure of the major organic product. Type of alkyl halide: Type of nucleophile: Solvent: Is the product racemic?
- Which of the following alkenes will produce more than one monobromination product in its free radical reaction with one molar equivalent NBS? Structure Structure Structure Structure StructureIgnoring stereoisomers, how many different mono-brominated substitution products can form by reaction of the compound shown below with NBS and light? (Consider all possible radicals and resonance forms.) 05 6 04 03 Onone of these SExplain why only the meso form of 1,2-dibromo-1,2-diphenylethane is formed.
- what is the product and mechanism used in this reaction?The reaction of 1-bromobutane with sodium hydroxide affords the substitution product butan-1-ol. What would happen to the rate of the reaction if the concentration of both 1-bromobutane and sodium hydroxide were doubled? The rate increases by a factor of 4. The rate decreases by a factor of 2. The rate remains the same. The rate increases by a factor of 2.For the following reaction there are three (3) possible products. Two of the products are expected to be minor and one product is expected to be a major product. Br H₂O Name and draw out the step-by-step mechanisms by which each of the products is formed. Briefly explain why one of the three products is expected to be a major product.