1 2 3 Acetanilide (A) Aniline (8) A nisole (C) Complete the following tables and Provide response to the accompanying qu

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1 2 3 Acetanilide (A) Aniline (8) A nisole (C) Complete the following tables and Provide response to the accompanying qu

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1 2 3 Acetanilide A Aniline 8 A Nisole C Complete The Following Tables And Provide Response To The Accompanying Qu 1
1 2 3 Acetanilide A Aniline 8 A Nisole C Complete The Following Tables And Provide Response To The Accompanying Qu 1 (55.56 KiB) Viewed 34 times
1 2 3 Acetanilide (A) Aniline (8) A nisole (C) Complete the following tables and Provide response to the accompanying questions. Show your work and all steps for questions involving calculations. This should be included in the result and discussion sections of your Lab Report. Sample: Group Name of Structure Mol. Wt Mass numbe Compound Compoun (g/mol) of r d (sample) (sample ) 4 5 1 2 3 4 "CH₂ نما 5 Product Group Products of number Acetanilide A Aniline B Anisole C Acetanilide A Aniline Acetanilide Aniline Anisole (sample Acetanilide Aniline NH₂ B Actual yield (g) None CH₁ N/A sampl e used (g) Percent yield (%) 0.347 9 Numbe r of moles of sample (mol.) Melting point (") 60°C Theoretica Reactio 1 yield of n time products (min) (g) Name of product 2,4-Dibromoanisole 1. Range the 3 benzene derivatives from the least to the most activating. 2. Determine the theoretical and percentage yield for all the products obtained from this experiment 3. Had you 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.
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