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- Show how m-toluidine can be converted tom-toluidineCH3 NH2the following compounds, using any necessary reagents.m-toluonitrileWhich set of reagents are most likely to affect the E2 elimination? a. CH3CH2O-, CH3CH2OH b. (CH3)3CO-, (CH3)3COHShow how m-toluidine can be converted tom-toluidineCH3 NH2the following compounds, using any necessary reagents.m-toluonitrile(a) CH3 C N CH3 CH2NH2m-methylbenzylamine(b)m-iodotolueneCH I 3 (c)m-cresol(d) CH3 OH3-methyl-4-nitroanilineCH3 NH2O2N(e)NHCH3N-cyclopentyl-m-toluidine
- Describe the given synthetic pathway. Discuss type of reactions involved, the purpose of each reagent, and the relevance of each step. Provide brief explanation. Create a retrosynthetic map for the synthetic pathway in Question 1.Which of the following is the strongest activating group in electrophilic aromatic substitution reactions? a) -CH2CH2OH b) –OCOCH3 c) –N(CH3)2 d) -N(CH3)3 e) -COOHPropose an efficient synthetic route for each of the following transformations (sketch each intermediate)