A researcher needed some N-methylbenzamide but only had sodium benzoate available. What reaction conditions could they use to convert their sodium benzoate to the desired product? 00 1.) SOCI₂, pyridine; 2.) CH3NH₂ 1.) H₂O, HCI; 2.) CH3NH2 1.) CH3NH₂; 2.) H₂O, HCI 1.) H₂ CrO4; 2.) NH3 NHCH3

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A researcher needed some N-methylbenzamide but only had sodium benzoate available. What reaction
conditions could they use to convert their sodium benzoate to the desired product?
1.) SOCI₂, pyridine; 2.) CH3NH₂
1.) H₂O, HCI; 2.) CH3NH₂
1.) CH3NH₂; 2.) H₂O, HCI
1.) H₂CrO4; 2.) NH3
NHCH3
Transcribed Image Text:A researcher needed some N-methylbenzamide but only had sodium benzoate available. What reaction conditions could they use to convert their sodium benzoate to the desired product? 1.) SOCI₂, pyridine; 2.) CH3NH₂ 1.) H₂O, HCI; 2.) CH3NH₂ 1.) CH3NH₂; 2.) H₂O, HCI 1.) H₂CrO4; 2.) NH3 NHCH3
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