
Concept explainers
(a)
Interpretation:
The structure of N-isopropylaniline is to be drawn.
Concept introduction:

Answer to Problem 23.1P
The structure of N-isopropylaniline is shown below.
Explanation of Solution
The name N-isopropylaniline indicates that it consists of the structure of aniline compound. One hydrogen atom of
Figure 1
The structure of N-isopropylaniline is shown in Figure 1.
(b)
Interpretation:
The structure of tert-butylamine is to be drawn.
Concept introduction:
Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are basic in nature because the nitrogen can donate its lone pairs and also the ability of the nitrogen to accept the proton in water.

Answer to Problem 23.1P
The structure of tert-butylamine is shown below.
Explanation of Solution
The name tert-butylamine indicates that it consist of tert-butyl group. The tert-butyl group is attached to an amine group. The structure of tert-butylamine is shown below.
Figure 2
The structure of tert-butylamine is shown in Figure 2.
(c)
Interpretation:
The structure of
Concept introduction:
Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are basic in nature because the nitrogen can donate its lone pairs and also the ability of the nitrogen to accept the proton in water.

Answer to Problem 23.1P
The structure of
Explanation of Solution
The name
Figure 3
The structure of
(d)
Interpretation:
The structure of
Concept introduction:
Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are basic in nature because the nitrogen can donate its lone pairs and also the ability of the nitrogen to accept the proton in water.

Answer to Problem 23.1P
The structure of
Explanation of Solution
The name
Figure 4
The structure of
(e)
Interpretation:
The structure of
Concept introduction:
Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are basic in nature because the nitrogen can donate its lone pairs and also the ability of the nitrogen to accept the proton in water.

Answer to Problem 23.1P
The structure of
Explanation of Solution
The name
Figure 5
The structure of
(f)
Interpretation:
The structure of
Concept introduction:
Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are basic in nature because the nitrogen can donate its lone pairs and also the ability of the nitrogen to accept the proton in water.

Answer to Problem 23.1P
The structure of
Explanation of Solution
The name
Figure 6
The structure of
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Chapter 23 Solutions
EBK ORGANIC CHEMISTRY
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- What alkene or alkyne yields the following products after oxidative cleavage with ozone? Click the "draw structure" button to launch the drawing utility. draw structure ... andarrow_forwardDraw the products of the stronger acid protonating the other reactant. H3C-C=C-4 NH2 KEq CH H3C `CH3 Product acid Product basearrow_forward2. Draw the missing structure(s) in each of the following reactions. The missing structure(s) can be a starting material or the major reaction product(s). C5H10 Br H-Br CH2Cl2 + enant.arrow_forward
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- 3 attempts left Check my work Draw the products formed in the following oxidative cleavage. [1] 03 [2] H₂O draw structure ... lower mass product draw structure ... higher mass productarrow_forward2. Draw the missing structure(s) in each of the following reactions. The missing structure(s) can be a starting material or the major reaction product(s). H-Br CH2Cl2arrow_forwardWrite the aldol condensation mechanism and product for benzaldehyde + cyclohexanone in a base. Then trans-cinnamaldehyde + acetone in base. Then, trans-cinnamaldehyde + cyclohexanone in a base.arrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning

