(a)
Interpretation:
The conversion of benzoic acid to benzylamine by using reductive amination is to be shown.
Concept introduction:
Reductive amination is also known as reductive alkylation. This is basically used for the conversion of a carbonyl group to an amine via an intermediate imine.
Reduction of amide is a process in which amide group is reduced to
(b)
Interpretation:
The conversion of benzaldehyde to benzylamine by using reductive amination is to be shown.
Concept introduction:
Reductive amination is also known as reductive alkylation. This is basically used for the conversion of a carbonyl group to an amine via an intermediate imine.
Reduction of amide is a process in which amide group is reduced to amines in the presence of reducing agents. Lithium aluminium hydride is a good reducing agent for such processes.
(c)
Interpretation:
The conversion of pyrrolidine to
Concept introduction:
Reductive amination is also known as reductive alkylation. This is basically used for the conversion of a carbonyl group to an amine via an intermediate imine.
Reduction of amide is a process in which amide group is reduced to amines in the presence of reducing agents. Lithium aluminium hydride is a good reducing agent for such processes.
(d)
Interpretation:
The conversion of cyclohexanone to
Concept introduction:
Reductive amination is also known as reductive alkylation. This is basically used for the conversion of a carbonyl group to an amine via an intermediate imine.
Reduction of amide is a process in which amide group is reduced to amines in the presence of reducing agents. Lithium aluminium hydride is a good reducing agent for such processes.
(e)
Interpretation:
The conversion of pentan
Concept introduction:
Reductive amination is also known as reductive alkylation. This is basically used for the conversion of a carbonyl group to an amine via an intermediate imine.
Reduction of amide is a process in which amide group is reduced to amines in the presence of reducing agents. Lithium aluminium hydride is a good reducing agent for such processes.
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- Which of these statements is NOT true about the reaction of amines with a cyclic anhydride like phthalic anhydride? a. Dimethylamine will give a cyclic imide product. b. Aniline will give a cyclic imide product. c. Triethylamine will give a cyclic imide product. d. The reaction undergoes a nucleophilic acyl substitution mechanism.arrow_forwardRank the following amines based on basicity Rationalize the electronic effects responsible for the basicity of aminesarrow_forwardShow how to prepare the following aromatic amines by aromatic nitration, followed by reduction. You may use benzene andtoluene as your aromatic starting materials. (c) m-bromoaniline (d) m-aminobenzoic acidarrow_forward
- Compare the physical properties of acid derivatives, and explain the unusually highboiling points and melting points of amides. Compare the relative reactivity ofesters, thioesters, amides, nitriles, anhydrides, and acid chloridesarrow_forwardA. The water solubility of amines found in medications can be increased by salt formation. Dextromethorphan hydrobromide, a cough suppresant, is the salt formed from dextromethorphan (XX) and hydrobromic acid (HBr). Write the equation for the formation of dextromethorphan hydrobromide. B. Suggest appropriate starting materials ( amine and alkyl halide) needed for the preparation of each of the following salts: 1. Cetylpyridinium chloride 2. Benzyldimethyltetradecylammonium chloridearrow_forwardWhy do you wash the dichloromethane solution of your reductive amination product with sodium bicarbonate, rather than dilute aqueous HCl? a) Sodium bicarbonate is a good method of removing aldehydes from organic solvent.b) The amine product will be protonated by acid and remain in the aqueous layer as a salt.c) Sodium bicarbonate transfers the amine starting material into the aqueous layer.d) Sodium bicarbonate reacts with leftover NaBH(OAc)3 and removes it from the mixture.arrow_forward
- Three of the following amines can be prepared by the Gabriel synthesis; three cannot. Write equations showing the successful applications of this method. (a) Butylamine (b) Isobutylamine (c) tert-Butylamine (d) 2-Phenylethylamine (e) N-Methylbenzylamine (f) Anilinearrow_forwardShow how to synthesize the following amines from the indicated starting materials below. Each of the final products may require several sequential steps. Draw the structure for each of the steps and show the reagents required.  Starting material Final product b) Benzene m-bromoaniline c) ethylbenzene p-ethylaniline + o-ethylaniline d) benzene p-bromoaniline + o-bromoanilinearrow_forwardShow how to prepare the following aromatic amines by aromatic nitration, followed by reduction. You may use benzene andtoluene as your aromatic starting materials. p-bromoanilinearrow_forward
- What is the effect of acid on the solubility of amines that are water-insoluble based on aniline and N, N-dimethylaniline?arrow_forwardgive the results of the following compounds after reaction with nitrous acid test a. primary aliphatic amine b. secondary aliphatic amine c. tertiary aliphatic amine d. primary aromatic aminearrow_forwardShow how to convert amines to other functional groups, and devise multistepsyntheses using amines as starting materials and intermediatesarrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning