(a)
Interpretation:
The structure of the carbonyl compound and the
Concept introduction:
The reaction between
(b)
Interpretation:
The structure of the carbonyl compound and the amine used to form the given imines is to be predicted.
Concept introduction:
The reaction between ketone/aldehyde and ammonia derivatives in mild acidic condition consists of two steps. The first step is the acid catalyzed addition of the amine to the carbonyl group. And the second step is acid catalyzed dehydration to get the desired product (an imine).
(c)
Interpretation:
The structure of the carbonyl compound and the amine used to form the given imine is to be predicted.
Concept introduction:
The reaction between ketone/aldehyde and ammonia derivatives in mild acidic condition consists of two steps. The first step is the acid catalyzed addition of the amine to the carbonyl group. And the second step is acid catalyzed dehydration to get the desired product (an imine).
(d)
Interpretation:
The structure of the carbonyl compound and the amine used to form the given imine is to be predicted.
Concept introduction:
The reaction between ketone/aldehyde and ammonia derivatives in mild acidic condition consists of two steps. The first step is the acid catalyzed addition of the amine to the carbonyl group. And the second step is acid catalyzed dehydration to get the desired product (an imine).
(e)
Interpretation:
The structure of the carbonyl compound and the amine used to form the given imine is to be predicted.
Concept introduction:
The reaction between ketone/aldehyde and ammonia derivatives in mild acidic condition consists of two steps. The first step is the acid catalyzed addition of the amine to the carbonyl group. And the second step is acid catalyzed dehydration to get the desired product (an imine).
(f)
Interpretation:
The structure of the carbonyl compound and the amine used to form the given imine is to be predicted.
Concept introduction:
The reaction between ketone/aldehyde and ammonia derivatives in mild acidic condition consists of two steps. The first step is the acid catalyzed addition of the amine to the carbonyl group. And the second step is acid catalyzed dehydration to get the desired product (an imine).
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Organic Chemistry (9th Edition)
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- Choose the correct phrase from the following One of the important methods for preparing cyclic amides is the reaction of Crignard reagent with cyclohexanone. The reaction of inulin with indole is given in an acidic medium that gives cyclic amide Caprolactam is a type of cyclic amide that can be prepared from cyclohexanearrow_forwardWhich of the following statements is correct? An aldehyde can react with a secondary amine through a nucleophilic addition-elimination mechanism to give an enamine product. A ketone can react with a secondary amine through a nucleophilic addition mechanism to give an imine product. An ketone can react with a primary amine through a nucleophilic addition-elimination mechanism to give an enamine product. An aldehyde can react with a primary amine through a nucleophilic addition mechanism to give an imine product.arrow_forwardBased on the image attached, it shows methyl salicylate reacts with Ethanamine, and Ether act as a solvent to form N-ethylbenzamide as a product. Explains the mechanism reaction of conversion ester to an amide.arrow_forward
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- Provide the reaction mechanisms and reagents used to carry out the synthesis of this molecule.arrow_forwardPrimary amines can also be prepared by the reaction of an alkyl halide with azide ion, followed by catalytic hydrogenation. What advantage do this method and the Gabriel synthesis have over the synthesis of a primary amine using an alkyl halide and ammonia?arrow_forwardShow how to convert carboxylic acids to other functional groups, and devisemultistep syntheses using carboxylic acids as starting materials and intermediates.Explain how acid chlorides are used as activated derivatives of carboxylic acidsarrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning