Pyridine (below) undergoes EAS reactions at a rate much slower than benzene, and the substitution eaction mostly occurs at position 3. Explain both of these observations, drawing all structures required to upport your reasoning. E+ E

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Q: Synthesize from benzene. (Hint: All of these require diazonium ions.) ) 4-methoxyaniline

A: Synthesize of 4-methoxyaniline from benzene.

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Q: 3- Identify the aromatic compounds and provide justification for your answers: s S. 2 Q

A: Aromaticity - It is clear that benzene is an especially stable compound. A number of other compounds…

Q: 2) Starting with benzene, outline a synthesis for each of the following: Z=O 0.1 0=2 b 0=6=0 -OH

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A: The nucleophilic substitution reaction of alkyl bromide with OH- is given below

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Q: What is the structure for (2R,3S)-2-bromo-1,3-pentanediol? OH I Br Br OH OH HO Br OI O II O III O IV…

A: Name : (2R,3S)-2-bromo-1,3-pentanediol

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Q: Chemistry 3. Complete the following reaction scheme. Give all product(s) and indicate major or minor…

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