12. If you theoretically performed the bromination of phenol with only one equivalent of Br₂, which product (ortho or pa
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12. If you theoretically performed the bromination of phenol with only one equivalent of Br₂, which product (ortho or pa
12. If you theoretically performed the bromination of phenol with only one equivalent of Br₂, which product (ortho or para) do you think would predominate? Hint: think about probability and statistics. 13. What product did you obtain from the competitive nitration of methyl benzoate? a. Which particular IR absorptions led you to this conclusion? b. How can the NMR signals in the aromatic region be used to confirm the identity of your product? repetiti oncent **** PUR 8.8 8.6 8.4 8.2 8.0 7.8 ppm 2.0 3.2 12 11 10 9 8 7 6 5 4 3 2 1 0 14. Explain why the -NHCOCH3 in acetanilide is only moderately activating while the -NH2 group in aniline is strongly activating 15. Why is it difficult to get triple nitrations of toluene like in the case of tri-nitro-toluene (TNT)? Int: 1.0 1.1
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