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3 cards from this section. Quick, good the night before a test.
What is the product formed when a nitro compound is reduced?
Think about the functional group that replaces the nitro group.
What type of amine do you produce from ammonia reacting with an alkyl halide?
Consider how many alkyl groups are added.
What is the primary product when a nitro compound undergoes reduction?
Think about what functional group replaces the nitro group.
True or False: The ammonolysis of an alkyl halide with ammonia can produce secondary amines.
Consider what happens when ammonia is limited.
Propose a synthetic route to convert a specific nitrile into a desired primary amine. Include all reagents, conditions, and expected yields.
Focus on the reduction conditions and expected reactants.
Evaluate the advantages of using Gabriel phthalimide synthesis over traditional amine synthesis methods.
Think about the implications of purity in reaction outcomes.
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