(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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Chapter 18 Solutions
Organic Chemistry Plus Masteringchemistry With Pearson Etext, Global Edition
- 7 Draw the starting alkyl bromide that would produce this alkyne under these conditions. F Drawing 1. NaNH2, A 2. H3O+ £ 4 Temps to rise Tomorrow Q Search H2arrow_forward7 Comment on the general features of the predicted (extremely simplified) ¹H- NMR spectrum of lycopene that is provided below. 00 6 57 PPM 3 2 1 0arrow_forwardIndicate the compound formula: dimethyl iodide (propyl) sulfonium.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningEBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENT


