(a)
Interpretation: The
Concept introduction: Gabriel synthesis is a method of preparation of primary
(b)
Interpretation: The alkyl halide needed to prepare the given primary amine by Gabriel synthesis is to be determined.
Concept introduction: Gabriel synthesis is a method of preparation of primary amines. This is a nucleophilic substitution reaction. The phthalimide in presence of base forms the resonance stabilized anion which acts as a nucleophile and attacks the electrophilic carbon of alkyl haides.
(c)
Interpretation: The alkyl halide needed to prepare the given primary amine by Gabriel synthesis is to be determined.
Concept introduction: Gabriel synthesis is a method of preparation of primary amines. This is a nucleophilic substitution reaction. The phthalimide in presence of base forms the resonance stabilized anion which acts as a nucleophile and attacks the electrophilic carbon of alkyl haides.
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ORGANIC CHEMISTRY
- What acetylide anion and alkyl halide can be used to prepare each alkyne? Indicate all possibilities when more than one route will work.arrow_forwardDraw the products formed when each compound is treated with one equivalent of HBr.arrow_forwardDraw the organic products formed when each alkyne is treated with two equivalents of HBr.arrow_forward
- What alkyl halides are formed when attached ether is treated with HBr?arrow_forward2. How many different ß-hydroxyaldehydes and ß-hydroxyketones, including constitutional isomers and stereoisomers, are formed upon treatment of a mixture of acetone and benzaldehyde with base? a. b. 2 c. 3 d. 4arrow_forwardGive the IUPAC name for each alkyne.arrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning